2012 Medtronic Coronary Catalog

Contents
W i n t e r 2 0 1 2
Coronary
Products
Catalog
Contents
At Medtronic, were committed to innovating for life by pushing the

boundaries of medical technology and changing the way the world treats
chronic disease. Our innovations help physicians diagnose diseases earlier,
treat patients with minimal disruptions and alleviate pain and symptoms
throughout patients lives. To do that, we think beyond the status quo
relentlessly seeking improved ways to help people live better, longer and
more productive lives.
The Medtronic CardioVascular business, our third largest, spans the major
specialties of interventional cardiology and cardiac and vascular surgery.
Our products, developed in collaboration with leading physicians, are used
to reduce the potentially debilitating effects of coronary, aortic and structural
heart disease.*
Through continued innovation and collaboration, we are pleased to offer one

of the most comprehensive coronary product portfolios for the treatment of
coronary artery disease.
Sincerely,
Jason Fontana
Vice President, U.S. Coronary Therapy
Strategy and Development
* This catalog only covers percutaneous coronary interventional products. Please contact
LifeLine CardioVascular Technical Support for information on other cardiovascular products.
Coronary Products Catalog
WINTER 2012
Drug-Eluting Stents
resolute integrity Zotarolimus-eluting Coronary Stent:
rX Coronary Stent System . . . . . . . . . . . . . . . . . . . . . . . . . 1
OtW Coronary Stent System . . . . . . . . . . . . . . . . . . . . . . . 3
endeavor Sprint Zotarolimus-eluting Coronary Stent:
Bare Metal Stents
integrity Bare Metal CoronaryStent:
Balloon Dilatation Catheters
Sprinter Legend Semicompliant. . . . . . . . . . . . . . . . . . . . . . . 11
Sprinter Legend 1.25 mm . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Sprinter OtW Semicompliant . . . . . . . . . . . . . . . . . . . . . . . . 13
nC Sprinter rX noncompliant . . . . . . . . . . . . . . . . . . . . . . . . 14
nC Stormer OtW noncompliant . . . . . . . . . . . . . . . . . . . . . . 15
Guide Catheters
Launcher Guide Catheters . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Left Coronary/17 Right Coronary/19 Radial/21 Other/22
Sherpa nX Guide Catheters
nX Active. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
nX Balanced. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Z2 Guide Catheters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Left Coronary/39 Right Coronary/41 Other/43
Zuma Guide Catheters . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Left Coronary/45 Right Coronary/47 Other/49
Embolic Protection
export AP Aspiration Catheter . . . . . . . . . . . . . . . . . . . . . . . 51
export Xt Aspiration Catheter . . . . . . . . . . . . . . . . . . . . . . . . 52
GuardWire temporary Occlusion and Aspiration System . . . . . . . 52
Interventional Guidewires (0.014 in.)
Zinger Stainless Steel Workhorse . . . . . . . . . . . . . . . . . . . . . . 53
intuition Stainless Steel Advanced Workhorse . . . . . . . . . . . . . . 55
Cougar nitinol Workhorse . . . . . . . . . . . . . . . . . . . . . . . . . . 56
thunder Stainless Steel extra-Support . . . . . . . . . . . . . . . . . . 57
ProVia Stainless Steel Crossing . . . . . . . . . . . . . . . . . . . . . . . 58
(continued on next page)

Contents
Contents, continued
Diagnostics and Accessories

Angiographic Catheters. . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
SiteSeer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
Pro-Flo . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70
Sones Woven Coronary Catheters . . . . . . . . . . . . . . . . . . . 80
Woven Coronary CathetersHigh-Volume . . . . . . . . . . . . . 83
Woven Coronary CathetersGeneral Purpose and
transvalvular Catheters . . . . . . . . . . . . . . . . . . . . . . . . . 84
Introducers
input tS introducer Sheaths . . . . . . . . . . . . . . . . . . . . . . . 85
input PS introducer Sheaths . . . . . . . . . . . . . . . . . . . . . . . 86
input Accessories (obturators, vessel dilators, sterile sleeves) . . 87
input SSV Split-Away Sheath with Valve and Side Port . . . . . . 88
transseptal Catheter introducer Sheaths . . . . . . . . . . . . . . . 89
Interventional Accessories
everest inflation Device and Survival Kit . . . . . . . . . . . . . . . . 91
Piton Disposable Adapters . . . . . . . . . . . . . . . . . . . . . . . . 92
Stretch insertion tool, Steering Handles . . . . . . . . . . . . . . . . 92
Pediatric Products
Pediatric Woven Coronary Catheters . . . . . . . . . . . . . . . . . . 93
Pediatric Woven niH Catheters . . . . . . . . . . . . . . . . . . . . . . 94
Pediatric rashkind Septostomy Balloon Catheters . . . . . . . . . 95
Brockenbrough needles. . . . . . . . . . . . . . . . . . . . . . . . . . 96
Pediatric Mullins transseptal introducer Sheath . . . . . . . . . . . 96
Hemodynamic Monitoring Catheter
Pulmonary Wedge Pressure (PWP) Catheter . . . . . . . . . . . . . 97
Angiographic Guidewires
Stainless Steel Guidewires . . . . . . . . . . . . . . . . . . . . . . . . . 99
PtFe-Coated Guidewires: Fixed Core . . . . . . . . . . . . . . . . . . 100
PtFe-Coated Guidewires: Movable Core . . . . . . . . . . . . . . . . 101
Heparin over PtFe-Coated Guidewires . . . . . . . . . . . . . . . . . 101
Specialty Guidewires . . . . . . . . . . . . . . . . . . . . . . . . . . . . 102
Transseptal Products
Brockenbrough needles . . . . . . . . . . . . . . . . . . . . . . . . . 105
transseptal Catheter introducer Sheaths. . . . . . . . . . . . . . . . 105
Contact and Ordering Information
Contact and Ordering information . . . . . . . . . . . . . . . . . . . . . 107

Reimbursement Tech Support Ordering Shipping Returns . . . 107
2011 Coronary Diagnostic and intervention Coding Sheet . . . . . . 109
ii
Contents
Drug-Eluting Coronary Stents
Resolute Integrity Drug-Eluting

RX Coronary Stent System General Characteristics:
Supplied sterile.
items per box: 1
Resolute Integrity DES, built on

0.69 mm (2.1 F) Minimal balloon
proximal shaft overhang the Integrity platform, delivers
a powerful antiproliferative,
zotarolimus, via the BioLinx
biocompatible polymer. The
low-profile, cobalt-alloy stent
is mounted on the extended
pressure, semicompliant,
0.91 mm (2.7 F) Proximal and distal RX MicroTrac delivery system.
distal shaft radiopaque markers
Resolute Integrity RX Ordering Information

Stent Length (mm)
Stent
Diameter (mm) 8 9 12 14 15 18 22 26 30
2.25 RSINT22508UX RSINT22512UX RSINT22514UX RSINT22518UX RSINT22522UX RSINT22526UX RSINT22530UX
Resolute Integrity RX Compliance

Stent Diameter
Deployed Stent i.D. (mm)
Pressure
(atm) 2.25 2.50 2.75 3.00 3.50 4.00
6 2.20 2.45 2.70 2.90 3.30 3.75
7 2.20 2.45 2.70 2.95 3.35 3.80
8 2.25 2.50 2.75 3.00 3.40 3.90
9 2.30 2.55 2.80 3.05 3.50 3.95
10 2.30 2.60 2.85 3.10 3.55 4.05
11 2.35 2.60 2.90 3.15 3.60 4.10
12 2.40 2.65 2.95 3.20 3.65 4.15
13 2.40 2.70 3.00 3.20 3.70 4.20
14 2.45 2.70 3.05 3.25 3.75 4.25
15 2.50 2.75 3.10 3.30 3.80 4.30
16 2.55 2.80 3.15 3.35 3.85 4.35
17 2.60 2.80 3.20 3.40 3.90 4.40
18 2.60 2.85 3.25 3.45 3.95 4.45
19 2.90 3.30 3.50 4.00 4.50
20 2.95 3.40 3.55 4.05
Nominal pressure Rated burst pressure*

Do not postdilate the 2.252.75-mm stents to greater than 3.50 mm.
Rated burst pressuredo not exceed.
*
Crossing profiles:
2.252.75 mm: 0.971.04 mm (0.0380.040 in.)
3.04.0 mm: 1.041.19 mm (0.0410.047 in.)
For distribution in the USA only.

1 2012 Medtronic, inc. All rights reserved. UC201204308en 2/12
CORONARY
Drug-Eluting Stents
Contents
Indications The safety and effectiveness of the Resolute Integrity stent have not yet been established in the following
The Resolute Integrity Zotarolimus-Eluting Coronary Stent System is indicated for improving coronary patient populations: Patients with target lesions which were treated with prior brachytherapy or the use
luminal diameters in patients, including those with diabetes mellitus, with symptomatic ischemic heart of brachytherapy to treat in-stent restenosis of a Resolute Integrity stent Women who are pregnant or
disease due to de novo lesions of length 27 mm in native coronary arteries with reference vessel lactating Men intending to father children Pediatric patients Patients with coronary artery reference
diameters of 2.25 mm to 4.20 mm. vessel diameters of <2.25 mm or >4.20 mm Patients with coronary artery lesions longer than 27 mm or
Contraindications requiring more than one Resolute Integrity stent Patients with evidence of an acute MI within 72 hours of
The Resolute Integrity Zotarolimus-Eluting Coronary Stent System is contraindicated for use in: Patients intended stent implantation Patients with vessel thrombus at the lesion site Patients with lesions located
with a known hypersensitivity or allergies to aspirin, heparin, bivalirudin, clopidogrel, prasugrel, ticagrelor, in a saphenous vein graft, in the left main coronary artery, ostial lesions, or bifurcation lesions Patients
ticlopidine, drugs such as zotarolimus, tacrolimus, sirolimus, everolimus or similar drugs or any other with diffuse disease or poor flow distal to identified lesions Patients with tortuous vessels in the region
analogue or derivative Patients with a known hypersensitivity to the cobalt-based alloy (cobalt, nickel, of the target vessel or proximal to the lesion Patients with in-stent restenosis Patients with moderate or
chromium and molybdenum) Patients with a known hypersensitivity to the BioLinx polymer or its severe lesion calcification at the target lesion Patients with occluded target lesions including chronic total
individual components occlusions Patients with three-vessel disease Patients with a left ventricular ejection fraction of <30%
Coronary artery stenting is contraindicated for use in: Patients in whom antiplatelet and/or Patients with a serum creatinine of >2.5mg/dl Patients with longer than 24 months of follow-up
anticoagulation therapy is contraindicated Patients who are judged to have a lesion that prevents The safety and effectiveness of the Resolute Integrity stent have not been established in the cerebral,
complete inflation of an angioplasty balloon or proper placement of the stent or stent delivery system carotid or peripheral vasculature.
warnings Potential Adverse Events
Please ensure that the inner package has not been opened or damaged as this would indicate the sterile Other risks associated with using this device are those associated with percutaneous coronary diagnostic
barrier has been breached. The use of this product carries the same risks associated with coronary artery (including angiography and IVUS) and treatment procedures. These risks (in alphabetical order) may
stent implantation procedures, which include subacute and late vessel thrombosis, vascular complications include but are not limited to: Abrupt vessel closure Access site pain, hematoma or hemorrhage
and/or bleeding events. This product should not be used in patients who are not likely to comply with the Allergic reaction (to contrast, antiplatelet therapy, stent material, or drug and polymer coating) Aneurysm,
recommended antiplatelet therapy. pseudoaneurysm, or arteriovenous fistula (AVF) Arrhythmias, including ventricular fibrillation Balloon
Precautions rupture Bleeding Cardiac tamponade Coronary artery occlusion, perforation, rupture or dissection
Only physicians who have received adequate training should perform implantation of the stent. Stent Coronary artery spasm Death Embolism (air, tissue, device or thrombus) Emergency surgery: peripheral
placement should only be performed at hospitals where emergency coronary artery bypass graft surgery vascular or coronary bypass Failure to deliver the stent Hemorrhage requiring transfusion Hypotension/
can be readily performed. Subsequent stent restenosis or occlusion may require repeat catheter-based hypertension Incomplete stent apposition Infection or fever MI Pericarditis Peripheral ischemia/
treatments (including balloon dilatation) of the arterial segment containing the stent. The long-term peripheral nerve injury Renal failure Restenosis of the stented artery Shock/pulmonary edema Stable
outcome following repeat catheter-based treatments of previously implanted endothelialized stents is or unstable angina Stent deformation, collapse, or fracture Stent migration (or embolization) Stent
not well characterized. The risks and benefits of the stent implantation should be assessed for patients misplacement Stroke/transient ischemic attack Thrombosis (acute, subacute or late)
with a history of severe reaction to contrast agents. Do not expose or wipe the product with organic Adverse Events Related to Zotarolimus
solvents such as alcohol. When drug-eluting stents (DES) are used outside the specified Indications for Use, Patients exposure to zotarolimus is directly related to the total amount of stent length implanted. The
patient outcomes may differ from the results observed in the RESOLUTE pivotal clinical trials. Compared actual side effects/complications that may be associated with the use of zotarolimus are not fully known.
to use within the specified Indications for Use, the use of DES in patients and lesions outside of the labeled The adverse events that have been associated with the intravenous injection of zotarolimus in humans
indications, including more tortuous anatomy, may have an increased risk of adverse events, including include but are not limited to: Anemia Diarrhea Dry skin Headache Hematuria Infection Injection
stent thrombosis, stent embolization, myocardial infarction (MI), or death Care should be taken to control site reaction Pain (abdominal, arthralgia, injection site) Rash
the position of the guide catheter tip during stent delivery, deployment, and balloon withdrawal. Before Please reference appropriate product Instructions for Use for more information regarding indications,
withdrawing the stent delivery system, visually confirm complete balloon deflation by fluoroscopy to avoid warnings, precautions and potential adverse events.
guiding catheter movement into the vessel and subsequent arterial damage Stent thrombosis is a low- CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.
frequency event that is frequently associated with MI or death. Data from the RESOLUTE clinical trials have
been prospectively evaluated and adjudicated using the definition developed by the Academic Research
Consortium (ARC).

CORONARY
Drug-Eluting Stents
Contents
Resolute Integrity Drug-Eluting

OTw Coronary Stent System General Characteristics:
Supplied sterile.
items per box: 1

proximal shaft overhang Resolute Integrity DES, built on
the Integrity platform, delivers
a powerful antiproliferative,
zotarolimus, via the BioLinx
biocompatible polymer. The
low-profile, cobalt-alloy stent
is mounted on the extended
0.91 mm (2.7 F) Proximal and distal pressure, semicompliant,
OTW MicroTrac delivery system.
Resolute Integrity OTw Ordering Information

Stent Stent Length (mm)
Diameter (mm) 8 9 12 14 15 18 22 26 30
2.25 RSINT22508W RSINT22512W RSINT22514W RSINT22518W RSINT22522W RSINT22526W RSINT22530W
Resolute Integrity OTw Compliance

Stent Diameter
Pressure
(atm) 2.25 2.50 2.75 3.00 3.50 4.00
6 2.20 2.45 2.70 2.90 3.30 3.75
7 2.20 2.45 2.70 2.95 3.35 3.80
8 2.25 2.50 2.75 3.00 3.40 3.90
9 2.30 2.55 2.80 3.05 3.50 3.95
10 2.30 2.60 2.85 3.10 3.55 4.05
11 2.35 2.60 2.90 3.15 3.60 4.10
12 2.40 2.65 2.95 3.20 3.65 4.15
13 2.40 2.70 3.00 3.20 3.70 4.20
14 2.45 2.70 3.05 3.25 3.75 4.25
15 2.50 2.75 3.10 3.30 3.80 4.30
16 2.55 2.80 3.15 3.35 3.85 4.35
17 2.60 2.80 3.20 3.40 3.90 4.40
18 2.60 2.85 3.25 3.45 3.95 4.45
19 2.90 3.30 3.50 4.00 4.50
20 2.95 3.40 3.55 4.05

*
Crossing profiles:
2.252.75 mm: 0.971.04 mm (0.0380.040 in.)
3.04.0 mm: 1.041.19 mm (0.0410.047 in.)

CORONARY
Drug-Eluting Stents
Contents
Indications The safety and effectiveness of the Resolute Integrity stent have not yet been established in the following
The Resolute Integrity Zotarolimus-Eluting Coronary Stent System is indicated for improving coronary patient populations: Patients with target lesions which were treated with prior brachytherapy or the use
luminal diameters in patients, including those with diabetes mellitus, with symptomatic ischemic heart of brachytherapy to treat in-stent restenosis of a Resolute Integrity stent Women who are pregnant or
disease due to de novo lesions of length 27 mm in native coronary arteries with reference vessel lactating Men intending to father children Pediatric patients Patients with coronary artery reference
diameters of 2.25 mm to 4.20 mm. vessel diameters of <2.25 mm or >4.20 mm Patients with coronary artery lesions longer than 27 mm or
Contraindications requiring more than one Resolute Integrity stent Patients with evidence of an acute MI within 72 hours of
The Resolute Integrity Zotarolimus-Eluting Coronary Stent System is contraindicated for use in: Patients intended stent implantation Patients with vessel thrombus at the lesion site Patients with lesions located
with a known hypersensitivity or allergies to aspirin, heparin, bivalirudin, clopidogrel, prasugrel, ticagrelor, in a saphenous vein graft, in the left main coronary artery, ostial lesions, or bifurcation lesions Patients
ticlopidine, drugs such as zotarolimus, tacrolimus, sirolimus, everolimus or similar drugs or any other with diffuse disease or poor flow distal to identified lesions Patients with tortuous vessels in the region
analogue or derivative Patients with a known hypersensitivity to the cobalt-based alloy (cobalt, nickel, of the target vessel or proximal to the lesion Patients with in-stent restenosis Patients with moderate or
chromium and molybdenum) Patients with a known hypersensitivity to the BioLinx polymer or its severe lesion calcification at the target lesion Patients with occluded target lesions including chronic total
individual components occlusions Patients with three-vessel disease Patients with a left ventricular ejection fraction of <30%
Coronary artery stenting is contraindicated for use in: Patients in whom antiplatelet and/or Patients with a serum creatinine of >2.5mg/dl Patients with longer than 24 months of follow-up
anticoagulation therapy is contraindicated Patients who are judged to have a lesion that prevents The safety and effectiveness of the Resolute Integrity stent have not been established in the cerebral,
complete inflation of an angioplasty balloon or proper placement of the stent or stent delivery system carotid or peripheral vasculature.
warnings Potential Adverse Events
Please ensure that the inner package has not been opened or damaged as this would indicate the sterile Other risks associated with using this device are those associated with percutaneous coronary diagnostic
barrier has been breached. The use of this product carries the same risks associated with coronary artery (including angiography and IVUS) and treatment procedures. These risks (in alphabetical order) may
stent implantation procedures, which include subacute and late vessel thrombosis, vascular complications include but are not limited to: Abrupt vessel closure Access site pain, hematoma or hemorrhage
and/or bleeding events. This product should not be used in patients who are not likely to comply with the Allergic reaction (to contrast, antiplatelet therapy, stent material, or drug and polymer coating) Aneurysm,
recommended antiplatelet therapy. pseudoaneurysm, or arteriovenous fistula (AVF) Arrhythmias, including ventricular fibrillation Balloon
Precautions rupture Bleeding Cardiac tamponade Coronary artery occlusion, perforation, rupture or dissection
Only physicians who have received adequate training should perform implantation of the stent. Stent Coronary artery spasm Death Embolism (air, tissue, device or thrombus) Emergency surgery: peripheral
placement should only be performed at hospitals where emergency coronary artery bypass graft surgery vascular or coronary bypass Failure to deliver the stent Hemorrhage requiring transfusion Hypotension/
can be readily performed. Subsequent stent restenosis or occlusion may require repeat catheter-based hypertension Incomplete stent apposition Infection or fever MI Pericarditis Peripheral ischemia/
treatments (including balloon dilatation) of the arterial segment containing the stent. The long-term peripheral nerve injury Renal failure Restenosis of the stented artery Shock/pulmonary edema Stable
outcome following repeat catheter-based treatments of previously implanted endothelialized stents is or unstable angina Stent deformation, collapse, or fracture Stent migration (or embolization) Stent
not well characterized. The risks and benefits of the stent implantation should be assessed for patients misplacement Stroke/transient ischemic attack Thrombosis (acute, subacute or late)
with a history of severe reaction to contrast agents. Do not expose or wipe the product with organic Adverse Events Related to Zotarolimus
solvents such as alcohol. When drug-eluting stents (DES) are used outside the specified Indications for Use, Patients exposure to zotarolimus is directly related to the total amount of stent length implanted. The
patient outcomes may differ from the results observed in the RESOLUTE pivotal clinical trials. Compared actual side effects/complications that may be associated with the use of zotarolimus are not fully known.
to use within the specified Indications for Use, the use of DES in patients and lesions outside of the labeled The adverse events that have been associated with the intravenous injection of zotarolimus in humans
indications, including more tortuous anatomy, may have an increased risk of adverse events, including include but are not limited to: Anemia Diarrhea Dry skin Headache Hematuria Infection Injection
stent thrombosis, stent embolization, myocardial infarction (MI), or death Care should be taken to control site reaction Pain (abdominal, arthralgia, injection site) Rash
the position of the guide catheter tip during stent delivery, deployment, and balloon withdrawal. Before Please reference appropriate product Instructions for Use for more information regarding indications,
withdrawing the stent delivery system, visually confirm complete balloon deflation by fluoroscopy to avoid warnings, precautions and potential adverse events.
guiding catheter movement into the vessel and subsequent arterial damage Stent thrombosis is a low- CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.
frequency event that is frequently associated with MI or death. Data from the RESOLUTE clinical trials have
been prospectively evaluated and adjudicated using the definition developed by the Academic Research
Consortium (ARC).

CORONARY
Drug-Eluting Stents
Contents
Endeavor Sprint Zotarolimus-Eluting

RX Coronary Stent System General Characteristics:
Supplied sterile.
items per box: 1
3.0 F intermediate shaft 3.3 F proximal shaft Minimal balloon overhang
The Endeavor zotarolimus-eluting
coronary stent system is a low-
profile, modular, cobalt alloy
drug-eluting stent that effectively
combines the deliverability of the
Driver stent platform with a highly
lipophilic sirolimus analog and a
clinically established PC polymer.
2.7 F distal shaft Proximal and The Endeavor stent is mounted on
distal radiopaque an extended-pressure, semi-
markers compliant rapid exchange delivery
system and features minimal
balloon overhang.
Endeavor Sprint RX Ordering Information
Balloon Length (mm) Crossing Profile O.D.
Diameter (mm) 8 9 12 14 15 18 24 30 mm (in.)
2.50 ENSP25008UX ENSP25012UX ENSP25014UX ENSP25018UX ENSP25024UX ENSP25030UX 1.021.04 (0.0400.041)
Endeavor Sprint RX Compliance

Pressure Deployed Stent I.D. (mm) Technical Information
(atm) 5 F minimum guide catheter i.D.: 1.4 mm (0.056 in.)
2.50 3.00 3.50
6 2.43 2.88 3.31
Nominal pressure
7 2.48 2.93 3.36
8 2.53 2.99 3.43 Rated burst pressure*
9 2.58 3.05 3.49
10 2.62 3.11 3.56 * Rated burst pressuredo not exceed.
Test data on file at Medtronic, Inc.
11 2.65 3.15 3.60
CAUTION: Do not dilate the stent beyond
12 2.69 3.18 3.64 Nominal pressure: the pressure these limits.
13 2.72 3.22 3.68 at which the balloon reaches its
labeled diameter. Rated burst Nominal Dilatation
14 2.75 3.25 3.71 pressure: the maximum pressure Stent Diameter Limits
15 2.79 3.29 3.75 to which a balloon is designed to 2.5 mm 3.0 mm
16 2.83 3.33 3.78 be inflated (95% confidence 3.0 mm 3.5 mm
that 99.9% will not fail below 3.5 mm 4.0 mm
17 2.86 3.37 3.82 rated burst pressure).
Indications an increased risk of adverse events, including stent thrombosis, stent embolization, MI, or death.
The Endeavor Sprint Zotarolimus-Eluting Coronary Stent Delivery System is indicated for improving The safety and effectiveness of the Endeavor stent have not yet been established in the following patient
coronary luminal diameter in patients with ischemic heart disease due to de novo lesions of length 27 mm populations:
in native coronary arteries with reference vessel diameters of 2.5 mm to 3.5 mm. Women who are pregnant or lactating Men intending to father children Pediatric patients Patients
with vessel thrombus at the lesion site Patients with coronary artery reference vessel diameters <2.5 mm
Contraindications or >3.5 mm Patients with coronary artery lesions longer than 27 mm or requiring more than one Endeavor
The Endeavor Zotarolimus-Eluting Coronary Stent System is contraindicated for use in: stent Patients with lesions located in saphenous vein grafts, in the unprotected left main coronary artery,
Patients with a known hypersensitivity to zotarolimus or structurally-related compounds Patients with ostial lesions, or lesions located at a bifurcation Patients with diffuse disease or poor flow distal to the
a known hypersensitivity to the cobalt-based alloy (cobalt, nickel, chromium, and molybdenum) Patients identified lesions Patients with multivessel disease Patients with tortuous vessels in the region of the
with a known hypersensitivity to Phosphorylcholine polymer or its individual components. obstruction or proximal to the lesion Patients with a recent acute myocardial infarction where there is
Coronary artery stenting is contraindicated for use in: evidence of thrombus or poor flow Patients for longer than 48 months of follow-up Patients with in-stent
Patients with a known hypersensitivity or allergies to aspirin, heparin, clopidogrel or ticlopidine Patients restenosis Patients with moderate or severe calcification in the lesion or a chronic total occlusion Patients
who cannot receive recommended antiplatelet and/or anticoagulation therapy Patients who are judged with prior brachytherapy of the target lesion or the use of brachytherapy to treat in-stent restenosis in an
to have a lesion that prevents complete inflation of an angioplasty balloon or proper placement of the Endeavor stent.
stent or stent delivery system.
The safety and effectiveness of the Endeavor stent have not been established in the cerebral, carotid, or
warnings peripheral vasculature.
Please ensure that the inner package has not been opened or damaged, as this indicates the sterile barrier
has been breached The use of this product carries the risks associated with coronary artery stenting, Potential Adverse Events
including subacute thrombosis, vascular complications, and/or bleeding events This product should not Other risks associated with using this device are those associated with percutaneous coronary diagnostic
be used in patients who are not likely to comply with the recommended antiplatelet therapy. (including angiography and IVUS) and treatment procedures. These risks may include, but are not limited
to Abrupt vessel closure Access site pain, hematoma or hemorrhage Allergic reaction (to contrast,
Precautions antiplatelet therapy, stent material, or drug and polymer coating) Aneurysm, pseudoaneurysm, or
Only physicians who have received adequate training should perform implantation of the stent Stent arteriovenous fistula (AVF) Arrhythmias Balloon rupture Cardiac tamponade Coronary artery occlusion,
placement should only be performed at hospitals where emergency coronary artery bypass graft surgery perforation, rupture, or dissection Coronary artery spasm Death Embolism (air, tissue, device, or
can be readily performed Subsequent stent blockage may require repeat dilatation of the arterial segment thrombus) Emergency surgery: peripheral vascular or coronary bypass Failure to deliver the stent
containing the stent. The long-term outcome following repeat dilatation of endothelialized stents is not Hemorrhage requiring transfusion Hypotension/hypertension Incomplete stent apposition Infection or
well characterized Risks and benefits of the stent should be assessed for patients with history of severe fever Late or very late thrombosis Myocardial infarction (MI) Myocardial ischemia Peripheral ischemia/
reaction to contrast agents Do not expose or wipe the product with organic solvents such as alcohol or peripheral nerve injury Renal failure Restenosis of the stented artery Rupture of native or bypass graft
detergents Stent thrombosis is a low-frequency event that current drug-eluting stent (DES) clinical trials Shock/pulmonary edema Stent deformation, collapse, or fracture Stent migration Stent misplacement
are not adequately powered to fully characterize. Stent thrombosis is frequently associated with myocardial Stroke/transient ischemic attack Thrombosis (acute and subacute) Unstable angina Ventricular
infarction (MI) or death. Data from the ENDEAVOR randomized clinical trials have been prospectively fibrillation.
evaluated and adjudicated using both the protocol definition of stent thrombosis and the definition
developed by the Academic Research Consortium (ARC), and demonstrate specific patterns of stent Adverse Events Related to Zotarolimus
thrombosis that vary depending on the definition used. In the ENDEAVOR clinical trials analyzed to date, the Patients exposure to zotarolimus is directly related to the total amount of stent length implanted. The
differences in the incidence of stent thrombosis observed with the Endeavor stent compared to bare metal actual side effects/complications that may be associated with the use of zotarolimus are not fully known.
stents have not been associated with an increased risk of cardiac death, MI, or all-cause mortality. Additional The adverse events that have been associated with the intravenous injection of zotarolimus in humans
data from longer-term follow-up in the ENDEAVOR randomized clinical trials and analyses of DES-related include Anemia Application site reaction Diarrhea Dry skin Headache Hematuria Infection
stent thrombosis are expected and should be considered in making treatment decisions as data become Injection site reaction Pain (abdominal, arthralgia, injection site) Rash.
available When DES are used outside the specified Indications for Use, patient outcomes may differ from the Please reference appropriate product Instructions for Use for more information regarding indications,
results observed in the pivotal clinical trials Compared to use within the specified Indications for Use, the use warnings, precautions and potential adverse events.
of DES in patients and lesions outside of the labeled indications, including more tortuous anatomy, may have CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.

CORONARY
Drug-Eluting Stents
Contents
Endeavor Sprint Zotarolimus-Eluting

OTw Coronary Stent System General Characteristics:
Supplied sterile.
items per box: 1
3.0 F intermediate shaft 3.3 F proximal Minimal balloon overhang
shaft The Endeavor zotarolimus-eluting
coronary stent system is a low-
profile, modular, cobalt alloy
drug-eluting stent that effectively
combines the deliverability of the
Driver stent platform with a highly
lipophilic sirolimus analog and a
clinically established PC polymer.
2.7 F distal shaft Proximal and The Endeavor stent is mounted on
distal radiopaque an extended-pressure, semi-
markers compliant over-the-wire delivery
system and features minimal
balloon overhang.
Endeavor Sprint OTw Ordering Information
Balloon Length (mm) Crossing Profile O.D.
Diameter (mm) 8 9 12 14 15 18 24 30 mm (in.)
2.50 ENSP25008W ENSP25012W ENSP25014W ENSP25018W ENSP25024W ENSP25030W 1.021.04 (0.0400.041)
Endeavor Sprint OTw Compliance

Pressure Deployed Stent I.D. (mm) Technical Information
(atm) 5 F minimum guide catheter i.D.: 1.4 mm (0.056 in.)
2.50 3.00 3.50
6 2.43 2.88 3.31
Nominal pressure
7 2.48 2.93 3.36
8 2.53 2.99 3.43 Rated burst pressure*
9 2.58 3.05 3.49
10 2.62 3.11 3.56 * Rated burst pressuredo not exceed.
11 2.65 3.15 3.60
CAUTION: Do not dilate the stent beyond
12 2.69 3.18 3.64 Nominal pressure: the pressure these limits.
13 2.72 3.22 3.68 at which the balloon reaches its
labeled diameter. Rated burst Nominal Dilatation
14 2.75 3.25 3.71 pressure: the maximum pressure Stent Diameter Limits
15 2.79 3.29 3.75 to which a balloon is designed to 2.5 mm 3.0 mm
16 2.83 3.33 3.78 be inflated (95% confidence 3.0 mm 3.5 mm
that 99.9% will not fail below 3.5 mm 4.0 mm
17 2.86 3.37 3.82 rated burst pressure).
Indications an increased risk of adverse events, including stent thrombosis, stent embolization, MI, or death.
The Endeavor Sprint Zotarolimus-Eluting Coronary Stent Delivery System is indicated for improving The safety and effectiveness of the Endeavor stent have not yet been established in the following patient
coronary luminal diameter in patients with ischemic heart disease due to de novo lesions of length 27 mm populations:
in native coronary arteries with reference vessel diameters of 2.5 mm to 3.5 mm. Women who are pregnant or lactating Men intending to father children Pediatric patients Patients
with vessel thrombus at the lesion site Patients with coronary artery reference vessel diameters <2.5 mm
Contraindications or >3.5 mm Patients with coronary artery lesions longer than 27 mm or requiring more than one Endeavor
The Endeavor Zotarolimus-Eluting Coronary Stent System is contraindicated for use in: stent Patients with lesions located in saphenous vein grafts, in the unprotected left main coronary artery,
Patients with a known hypersensitivity to zotarolimus or structurally-related compounds Patients with ostial lesions, or lesions located at a bifurcation Patients with diffuse disease or poor flow distal to the
a known hypersensitivity to the cobalt-based alloy (cobalt, nickel, chromium, and molybdenum) Patients identified lesions Patients with multivessel disease Patients with tortuous vessels in the region of the
with a known hypersensitivity to Phosphorylcholine polymer or its individual components. obstruction or proximal to the lesion Patients with a recent acute myocardial infarction where there is
Coronary artery stenting is contraindicated for use in: evidence of thrombus or poor flow Patients for longer than 48 months of follow-up Patients with in-stent
Patients with a known hypersensitivity or allergies to aspirin, heparin, clopidogrel or ticlopidine Patients restenosis Patients with moderate or severe calcification in the lesion or a chronic total occlusion Patients
who cannot receive recommended antiplatelet and/or anticoagulation therapy Patients who are judged with prior brachytherapy of the target lesion or the use of brachytherapy to treat in-stent restenosis in an
to have a lesion that prevents complete inflation of an angioplasty balloon or proper placement of the Endeavor stent.
stent or stent delivery system.
The safety and effectiveness of the Endeavor stent have not been established in the cerebral, carotid, or
warnings peripheral vasculature.
Please ensure that the inner package has not been opened or damaged, as this indicates the sterile barrier
has been breached The use of this product carries the risks associated with coronary artery stenting, Potential Adverse Events
including subacute thrombosis, vascular complications, and/or bleeding events This product should not Other risks associated with using this device are those associated with percutaneous coronary diagnostic
be used in patients who are not likely to comply with the recommended antiplatelet therapy. (including angiography and IVUS) and treatment procedures. These risks may include, but are not limited
to Abrupt vessel closure Access site pain, hematoma or hemorrhage Allergic reaction (to contrast,
Precautions antiplatelet therapy, stent material, or drug and polymer coating) Aneurysm, pseudoaneurysm, or
Only physicians who have received adequate training should perform implantation of the stent Stent arteriovenous fistula (AVF) Arrhythmias Balloon rupture Cardiac tamponade Coronary artery occlusion,
placement should only be performed at hospitals where emergency coronary artery bypass graft surgery perforation, rupture, or dissection Coronary artery spasm Death Embolism (air, tissue, device, or
can be readily performed Subsequent stent blockage may require repeat dilatation of the arterial segment thrombus) Emergency surgery: peripheral vascular or coronary bypass Failure to deliver the stent
containing the stent. The long-term outcome following repeat dilatation of endothelialized stents is not Hemorrhage requiring transfusion Hypotension/hypertension Incomplete stent apposition Infection or
well characterized Risks and benefits of the stent should be assessed for patients with history of severe fever Late or very late thrombosis Myocardial infarction (MI) Myocardial ischemia Peripheral ischemia/
reaction to contrast agents Do not expose or wipe the product with organic solvents such as alcohol or peripheral nerve injury Renal failure Restenosis of the stented artery Rupture of native or bypass graft
detergents Stent thrombosis is a low-frequency event that current drug-eluting stent (DES) clinical trials Shock/pulmonary edema Stent deformation, collapse, or fracture Stent migration Stent misplacement
are not adequately powered to fully characterize. Stent thrombosis is frequently associated with myocardial Stroke/transient ischemic attack Thrombosis (acute and subacute) Unstable angina Ventricular
infarction (MI) or death. Data from the ENDEAVOR randomized clinical trials have been prospectively fibrillation.
evaluated and adjudicated using both the protocol definition of stent thrombosis and the definition
developed by the Academic Research Consortium (ARC), and demonstrate specific patterns of stent Adverse Events Related to Zotarolimus
thrombosis that vary depending on the definition used. In the ENDEAVOR clinical trials analyzed to date, the Patients exposure to zotarolimus is directly related to the total amount of stent length implanted. The
differences in the incidence of stent thrombosis observed with the Endeavor stent compared to bare metal actual side effects/complications that may be associated with the use of zotarolimus are not fully known.
stents have not been associated with an increased risk of cardiac death, MI, or all-cause mortality. Additional The adverse events that have been associated with the intravenous injection of zotarolimus in humans
data from longer-term follow-up in the ENDEAVOR randomized clinical trials and analyses of DES-related include Anemia Application site reaction Diarrhea Dry skin Headache Hematuria Infection
stent thrombosis are expected and should be considered in making treatment decisions as data become Injection site reaction Pain (abdominal, arthralgia, injection site) Rash.
available When DES are used outside the specified Indications for Use, patient outcomes may differ from the Please reference appropriate product Instructions for Use for more information regarding indications,
results observed in the pivotal clinical trials Compared to use within the specified Indications for Use, the use warnings, precautions and potential adverse events.
of DES in patients and lesions outside of the labeled indications, including more tortuous anatomy, may have CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.

Contents
Bare Metal Coronary Stents
Integrity RX Coronary Stent System

0.69 mm (2.1 F) Minimal balloon General Characteristics:
proximal shaft overhang
Supplied sterile.
items per box: 1
The Integrity bare metal coronary

stent system incorporates
continuous sinusoid technology
0.91 mm (2.7 F) Proximal and distal
in an advanced, low-profile cobalt
distal shaft radiopaque markers alloy stent that is mounted on the
extended-pressure, semicompliant
RX MicroTrac delivery system.
Integrity RX Ordering Information

Diameter (mm) 8 9 12 14 15 18 22 26 30
2.25 INT22508UX INT22512UX INT22514UX INT22518UX INT22522UX INT22526UX
3.00 INT30009UX INT30012UX INT30015UX INT30018UX INT30022UX INT30026UX INT30030UX
Integrity RX Compliance
Stent Diameter
Pressure
(atm) 2.25 2.50 2.75 3.00 3.50 4.00
6 2.15 2.40 2.65 2.85 3.25 3.70
7 2.20 2.45 2.70 2.90 3.30 3.75
8 2.20 2.50 2.75 2.95 3.40 3.85
9 2.25 2.55 2.80 3.05 3.45 3.90
10 2.30 2.55 2.85 3.10 3.50 4.00
11 2.35 2.60 2.90 3.10 3.55 4.05
12 2.35 2.65 2.90 3.15 3.60 4.10
13 2.40 2.65 2.95 3.20 3.65 4.15
14 2.45 2.70 3.00 3.25 3.65 4.20
15 2.50 2.75 3.05 3.30 3.70 4.25
16 2.50 2.80 3.10 3.30 3.75 4.30
17 2.55 2.80 3.15 3.35 3.80 4.35
18 2.60 2.85 3.20 3.40 3.85 4.40
19 2.65 2.90 3.25 3.45 3.90 4.45
20 2.75 2.95 3.30 3.50 3.90

*
Crossing profiles:
2.252.75 mm: 0.971.04 mm (0.0380.040 in.)
3.04.0 mm: 1.041.19 mm (0.0410.047 in.)

7 2011 Medtronic, inc. All rights reserved. UC201101771aen 10/11
CORONARY
Bare Metal Stents
Contents
Indications for Use The Integrity Coronary Stent Systems do not vascular complications and/or bleeding
The Integrity Coronary Stent Systems are provide for distal dye injections or pressure events. Administration of appropriate
indicated for improving coronary luminal measurements through the guidewire lumen. anticoagulant, antiplatelet and coronary
diameter in patients with symptomatic Expansion of the stent should not be vasodilator therapy is critical to successful
ischemic heart disease due to discrete de novo undertaken if the stent is not appropriately stent implantation and follow-up.
or restenotic lesions with reference vessel positioned in the vessel. If the position of Subsequent restenosis may require repeat
diameters of 2.254.0 mm and 30 mm in the stent is not optimal, it should not be dilatation of the arterial segment containing
length using direct stenting or predilatation. expanded. the stent. The long-term outcome following
Contraindications Incomplete deployment of the stent (i.e., stent repeat dilatation of endothelialized coronary
Patients in whom antiplatelet and/or not fully expanded) may cause procedural stents is unknown at present.
anticoagulation therapy is contraindicated complications resulting in patient injury. Potential Adverse Events
Patients who are judged to have a lesion that Advancement of an Integrity Coronary Stent The following complications may be associated
prevents complete inflation of an angioplasty System through a previously stented segment with the use of coronary stenting devices or
balloon or proper placement of a stent or stent may cause procedural complications resulting PTCA:
delivery system in patient injury. Acute myocardial infarction Allergic reaction
warnings/Precautions Placement of the stent has the potential to to contrast medium/stent material/medications
The long-term effects of stents and the risks compromise sidebranch patency. Arrhythmias (including ventricular fibrillation
associated with lifelong carrying of these Administer appropriate anticoagulant/ and ventricular tachycardia) Arteriovenous
implants are unknown. This lack of knowledge antiplatelet and coronary artery vasodilator fistula Bleeding complications Cardiac
should be considered in making a risk/benefit therapy according to current medical tamponade Cerebrovascular accident/stroke
assessment for the patient prior to implantation. guidelines and manufacturers instructions. Death Dissection of coronary artery Drug
The Integrity Coronary Stent Systems are Caution must be taken when using ancillary reactions Embolization (air, stent, tissue or
provided sterile, for one procedure only. Do equipment, such as intravascular ultrasound thrombotic) Emergency coronary artery
not resterilize. Use by the Use by date noted catheters, to avoid dislodgement or bypass graft surgery (CABG) Endocarditis
on the package. deformation of the stent. Failure to deliver the stent Stent deformation,
Only physicians who have received When multiple stents are required, stent collapse or fracture Hematoma Hemorrhage
appropriate training should perform materials should be of similar composition. requiring transfusion Injury of the coronary
implantation of the stent. Use of an Integrity Placing multiple stents of different materials artery Myocardial ischemia/infarction Pain
Coronary Stent System requires advanced in contact with each other may increase the and tenderness at the insertion site Perforation
coronary angioplasty technical skills. The potential for corrosion. Data obtained from Peripheral Ischemia Peripheral nerve injury
instructions will give technical guidance, but in vitro corrosion tests using a cobalt alloy Pseudoaneurysm (coronary/femoral/radial)
do not obviate the need for formal training in stent (Medtronic Integrity Coronary Stent) in Pyrogenic reaction Restenosis of the dilated
the use of the device. combination with a stainless steel alloy stent artery or stented segment Sepsis/infection
Patients allergic to cobalt alloy may suffer an (Boston Scientific Libert Coronary Stent) Short-term hemodynamic deterioration
allergic reaction to this implant. do not suggest an increased risk of in vivo (hypotension/hypertension) Stent thrombosis
Do not remove the stent from the stent corrosion. or occlusion Total occlusion of coronary artery
delivery system; the stent cannot be removed When using two wires, care should be taken Unstable angina Vascular thrombosis Vessel
and placed on another balloon catheter for when introducing, torquing and removing one dissection/perforation/spasm
deployment. or both guidewires to avoid entanglement. Please reference appropriate product
Do not try to straighten a kinked shaft or It is recommended that one guidewire be Instructions for Use for a more detailed list of
hypotube. Straightening a kinked metal shaft completely withdrawn from the patient before indications, warnings, precautions and potential
may result in breakage of the shaft. If the removing any additional equipment. adverse events.
device is kinked, it should not be used. Stent placement should only be performed
Significant amounts of air in the balloon may at hospitals where emergency coronary CAUTION: Federal (USA) law restricts this device
cause uneven expansion of the stent and artery bypass graft surgery can be readily to sale by or on the order of a physician.
difficulty in deployment of the stent. Do not performed.
pre-inflate balloon prior to stent deployment. Judicious selection of patients is necessary
Use balloon preparation technique described since the use of this device carries the
within this instructional material. associated risk of subacute thrombosis,

CORONARY
Bare Metal Stents
Contents
Integrity OTw Coronary Stent System General Characteristics:

Supplied sterile.
items per box: 1

proximal shaft overhang The Integrity bare metal coronary
stent system incorporates
continuous sinusoid technology
in an advanced, low-profile cobalt
alloy stent that is mounted on the
extended-pressure, semi-compliant
OTW MicroTrac delivery system.
0.91 mm (2.7 F) Proximal and distal
Integrity OTw Ordering Information

Diameter (mm) 8 9 12 14 15 18 22 26 30
2.25 INT22508W INT22512W INT22514W INT22518W INT22522W INT22526W
3.00 INT30009W INT30012W INT30015W INT30018W INT30022W INT30026W INT30030W
Integrity OTw Compliance

Stent Diameter
Pressure
(atm) 2.25 2.50 2.75 3.00 3.50 4.00
6 2.15 2.40 2.65 2.85 3.25 3.70
7 2.20 2.45 2.70 2.90 3.30 3.75
8 2.20 2.50 2.75 2.95 3.40 3.85
9 2.25 2.55 2.80 3.05 3.45 3.90
10 2.30 2.55 2.85 3.10 3.50 4.00
11 2.35 2.60 2.90 3.10 3.55 4.05
12 2.35 2.65 2.90 3.15 3.60 4.10
13 2.40 2.65 2.95 3.20 3.65 4.15
14 2.45 2.70 3.00 3.25 3.65 4.20
15 2.50 2.75 3.05 3.30 3.70 4.25
16 2.50 2.80 3.10 3.30 3.75 4.30
17 2.55 2.80 3.15 3.35 3.80 4.35
18 2.60 2.85 3.20 3.40 3.85 4.40
19 2.65 2.90 3.25 3.45 3.90 4.45
20 2.75 2.95 3.30 3.50 3.90

*
Crossing profiles:
2.252.75 mm: 0.971.04 mm (0.0380.040 in.)
3.04.0 mm: 1.041.19 mm (0.0410.047 in.)

CORONARY
Bare Metal Stents
Contents
Indications for Use The Integrity Coronary Stent Systems do not vascular complications and/or bleeding
The Integrity Coronary Stent Systems are provide for distal dye injections or pressure events. Administration of appropriate
indicated for improving coronary luminal measurements through the guidewire lumen. anticoagulant, antiplatelet and coronary
diameter in patients with symptomatic Expansion of the stent should not be vasodilator therapy is critical to successful
ischemic heart disease due to discrete de novo undertaken if the stent is not appropriately stent implantation and follow-up.
or restenotic lesions with reference vessel positioned in the vessel. If the position of Subsequent restenosis may require repeat
diameters of 2.254.0 mm and 30 mm in the stent is not optimal, it should not be dilatation of the arterial segment containing
length using direct stenting or predilatation. expanded. the stent. The long-term outcome following
Contraindications Incomplete deployment of the stent (i.e., stent repeat dilatation of endothelialized coronary
Patients in whom antiplatelet and/or not fully expanded) may cause procedural stents is unknown at present.
anticoagulation therapy is contraindicated complications resulting in patient injury. Potential Adverse Events
Patients who are judged to have a lesion that Advancement of an Integrity Coronary Stent The following complications may be associated
prevents complete inflation of an angioplasty System through a previously stented segment with the use of coronary stenting devices or
balloon or proper placement of a stent or stent may cause procedural complications resulting PTCA:
delivery system in patient injury. Acute myocardial infarction Allergic reaction
warnings/Precautions Placement of the stent has the potential to to contrast medium/stent material/medications
The long-term effects of stents and the risks compromise sidebranch patency. Arrhythmias (including ventricular fibrillation
associated with lifelong carrying of these Administer appropriate anticoagulant/ and ventricular tachycardia) Arteriovenous
implants are unknown. This lack of knowledge antiplatelet and coronary artery vasodilator fistula Bleeding complications Cardiac
should be considered in making a risk/benefit therapy according to current medical tamponade Cerebrovascular accident/stroke
assessment for the patient prior to implantation. guidelines and manufacturers instructions. Death Dissection of coronary artery Drug
The Integrity Coronary Stent Systems are Caution must be taken when using ancillary reactions Embolization (air, stent, tissue or
provided sterile, for one procedure only. Do equipment, such as intravascular ultrasound thrombotic) Emergency coronary artery
not resterilize. Use by the Use by date noted catheters, to avoid dislodgement or bypass graft surgery (CABG) Endocarditis
on the package. deformation of the stent. Failure to deliver the stent Stent deformation,
Only physicians who have received When multiple stents are required, stent collapse or fracture Hematoma Hemorrhage
appropriate training should perform materials should be of similar composition. requiring transfusion Injury of the coronary
implantation of the stent. Use of an Integrity Placing multiple stents of different materials artery Myocardial ischemia/infarction Pain
Coronary Stent System requires advanced in contact with each other may increase the and tenderness at the insertion site Perforation
coronary angioplasty technical skills. The potential for corrosion. Data obtained from Peripheral Ischemia Peripheral nerve injury
instructions will give technical guidance, but in vitro corrosion tests using a cobalt alloy Pseudoaneurysm (coronary/femoral/radial)
do not obviate the need for formal training in stent (Medtronic Integrity Coronary Stent) in Pyrogenic reaction Restenosis of the dilated
the use of the device. combination with a stainless steel alloy stent artery or stented segment Sepsis/infection
Patients allergic to cobalt alloy may suffer an (Boston Scientific Libert Coronary Stent) Short-term hemodynamic deterioration
allergic reaction to this implant. do not suggest an increased risk of in vivo (hypotension/hypertension) Stent thrombosis
Do not remove the stent from the stent corrosion. or occlusion Total occlusion of coronary artery
delivery system; the stent cannot be removed When using two wires, care should be taken Unstable angina Vascular thrombosis Vessel
and placed on another balloon catheter for when introducing, torquing and removing one dissection/perforation/spasm
deployment. or both guidewires to avoid entanglement. Please reference appropriate product
Do not try to straighten a kinked shaft or It is recommended that one guidewire be Instructions for Use for a more detailed list of
hypotube. Straightening a kinked metal shaft completely withdrawn from the patient before indications, warnings, precautions and potential
may result in breakage of the shaft. If the removing any additional equipment. adverse events.
device is kinked, it should not be used. Stent placement should only be performed
Significant amounts of air in the balloon may at hospitals where emergency coronary CAUTION: Federal (USA) law restricts this device
cause uneven expansion of the stent and artery bypass graft surgery can be readily to sale by or on the order of a physician.
difficulty in deployment of the stent. Do not performed.
pre-inflate balloon prior to stent deployment. Judicious selection of patients is necessary
Use balloon preparation technique described since the use of this device carries the
within this instructional material. associated risk of subacute thrombosis,

Contents
Sprinter Legend Semicompliant Balloon Dilatation Catheter

Over-the-wire luer Gold-swaged Proximal shaft Platinum iridium Proximal shaft (oval) General Characteristics:
marker bands marker bands
Supplied sterile.
Items per box: 1
RX luer
Flexible FasTrac tip Flexible FasTrac tip design
Dura-Trac
hydrophilic Fulcrum Dura-Trac
Distal shaft coating balloon material hydrophilic
Distal shaft coating
Sprinter Legend RX Ordering Information
Balloon Balloon Length (mm) Crossing Profile
Diameter (mm) 6 10 12 15 20 25 30 O.D. mm (in.)
1.25 SPL12506X SPL12510X SPL12512X SPL12515X SPL12520X 0.5 (0.020)
2.00 SPL20006X SPL20010X SPL20012X SPL20015X SPL20020X SPL20025X SPL20030X 0.6 (0.022)
2.25 SPL22506X SPL22510X SPL22512X SPL22515X SPL22520X SPL22525X 0.6 (0.022)
3.25 SPL32512X SPL32515X SPL32520X 0.6 (0.023)
3.75 SPL37512X SPL37515X SPL37520X 0.6 (0.023)
Sprinter Legend OTW Ordering Information

Diameter (mm) 6 10 15 20 O.D. mm (in.)
1.25 SPL12506WL SPL12510WL SPL12515WL SPL12520WL 0.5 (0.020)
Sprinter Legend Compliance
Balloon Diameter (mm)
Pressure RX/OTW RX
(atm) 1.25 1.50 2.00 2.25 2.50 2.75 3.00 3.25 3.50 3.75 4.00
4 0.60 1.36
5 0.60 1.41 Nominal pressure.
6 0.63 1.47 1.91 2.23 2.34 2.60 2.81 3.14 3.32 3.61 3.85 Rated burst pressure
7 0.67 1.53 1.95 2.29 2.41 2.67 2.89 3.22 3.42 3.70 3.96 do not exceed.
Nominal pressure and
8 0.75 1.58 2.00 2.33 2.47 2.74 2.97 3.29 3.50 3.79 4.05 rated burst pressure are the same.
9 0.86 1.61 2.03 2.38 2.53 2.79 3.04 3.35 3.57 3.86 4.12
Nominal pressure: the pressure at
10 0.99 1.64 2.06 2.41 2.57 2.84 3.09 3.40 3.63 3.93 4.18 which the balloon reaches its labeled
11 1.11 1.67 2.09 2.44 2.61 2.89 3.14 3.44 3.68 3.98 4.23 diameter
12 1.20 1.70 2.12 2.47 2.64 2.93 3.18 3.48 3.73 4.02 4.29 Rated burst pressure: the maximum
13 1.28 1.73 2.14 2.51 2.67 2.96 3.22 3.52 3.77 4.07 4.35 pressure to which a balloon is
14 1.35 1.75 2.16 2.54 2.70 3.00 3.25 3.56 3.82 4.12 4.40 designed to be inflated (95%
confidence that 99.9% will not fail
15 1.40 1.78 2.19 2.58 2.73 3.03 3.29 3.59 3.87 4.16 4.45 below rated burst pressure)
16 2.21 2.61 2.76 3.07 3.33 3.64 3.92 4.21 4.50 Test data on file at Medtronic, Inc.
Compatible with 6 F Technical Information

kissing balloon technique. Catheter length RX 142 cm; OTW 152 cm Shaft O.D. for 1.253.50 mm
Distal shaft length RX 21 cm Proximal RX 1.9 F; OTW 3.2 F
Any combination of two Sprinter Legend
Platinum iridium marker bands Distal 2.4 F/2.6 F
rapid exchange balloon models (1.25
1.251.50 mm Single Shaft O.D. for 3.754.00 mm
3.50 mm) can be used for the kissing
2.004.00 mm Double Proximal RX 1.9 F; OTW 3.2 F
balloon technique within a 6 F (MGCID
Dura-Trac selective coating Distal 2.5 F/2.7 F
0.070) guide catheter. Test data on file at
MiniWrap MGCID 1.4 mm/.056"
Medtronic, Inc.
1.25 mm Zerofold
1.50 mm 2 folds
2.003.75 mm 3 folds
4.00 mm 5 folds

11 2011 Medtronic, Inc. All rights reserved. UC200903035aEN 6/11
CORONARY
Contents
Sprinter Legend 1.25 mm Semicompliant

Balloon Dilatation Catheter
General Characteristics:
Over-the-wire Gold-swaged Proximal shaft Platinum iridium
marker band
Proximal shaft Supplied sterile.
marker bands
items per box: 1
Flexible FasTrac tip design Product Description:

Flexible FasTrac tip
The Sprinter Legend 1.25-mm semi
Dura-Trac Dura-Trac compliant balloon dilatation catheter

hydrophilic
Distal shaft
hydrophilic
Distal shaft
coating
Fulcrum
balloon material coating with award-winning* SuperCrosser
Zerofold Technology.
Sprinter Legend 1.25 mm RX Ordering Information
Balloon Balloon Length (mm) Crossing
Diameter Profile O.D.
(mm) 6 10 12 15 20 mm (in.)
Sprinter Legend 1.25 mm OTw Ordering Information

Balloon Balloon Length (mm) Crossing
Diameter Profile O.D.
(mm) 6 10 15 20 mm (in.)
1.25 SPL12506WL SPL12510WL SPL12515WL SPL12520WL 0.5 (0.020)
Sprinter Legend 1.25 Compliance

Deployed Stent TECHNICAL INFORMATION
Pressure Nominal pressure
I.D. (mm) Catheter length RX 142 cm; OTW 152 cm
(atm) Distal shaft length RX 21 cm
1.25 Rated burst pressure
4 0.60 Platinum iridium marker bands
Nominal pressure and rated
1.25 mm Single
5 0.60 burst pressure are the same.
Dura-Trac selective coating
6 0.63 Test data on file at Medtronic, Inc.
MiniWrap

7 0.67 1.25 mm Zerofold

Nominal pressure: the pressure at which the Shaft dimensions for 1.25 mm
8 0.75 balloon reaches its labeled diameter. Proximal RX 1.9 F; OTW 3.2 F
9 0.86 Rated burst pressure: the maximum pressure to Distal 2.4 F/2.6 F
which a balloon is designed to be inflated
10 0.99 (95% confidence that 99.9% will not fail below MGCID 1.4 mm/.056
rated burst pressure).
11 1.11
12 1.20
13 1.28
14 1.35
15 1.40
16
The Lowest Crossing Profile on the Market

Lesion entry profile: 0.41 mm (0.016")
Crossing profile: 0.5 mm (0.020")
Profile over mid-marker: 0.6 mm (0.024")
SuperCrosser Zerofold Technology 0.5-mm (0.020")

(no balloon wrap or shoulders) crossing profile
Micro-Brite 0.41-mm (0.016")

low-profile marker band FasTrac tapered tip
* Medtronic CardioVascular in Ireland was selected as the overall winner of the

In testing vs. US competitors.
Innovation Company of the Year Award 2007 for its SuperCrosser Zerofold Technology by Test data on file at Medtronic, Inc. Bench testing may not
The Institution of Engineers of Ireland. be indicative of clinical performance.

CORONARY
Contents
Sprinter OTw Semicompliant

Proximal shaft
Supplied sterile.
items per box: 1
Gold-swaged marker bands
Dura-Trac
hydrophilic Fulcrum
Distal shaft coating balloon material
Sprinter OTw Ordering Information

Balloon Balloon Length (mm) Crossing Profile O.D.
Diameter (mm) 6 10 12 15 20 25 30 mm (in.)
1.50 SPR1506W SPR1510W SPR1512W SPR1515W SPR1520W 0.53 (0.021)
2.00 SPR2006W SPR2010W SPR2012W SPR2015W SPR2020W SPR2025W SPR2030W 0.56 (0.022)
2.25 SPR22506W SPR22512W SPR22515W SPR22520W 0.56 (0.022)
2.75 SPR27506W SPR27512W SPR27515W SPR27520W 0.58 (0.023)
3.25 SPR32512W SPR32515W SPR32520W 0.58 (0.023)
3.75 SPR37512W SPR37515W SPR37520W 0.58 (0.023)
Sprinter OTw Compliance

Pressure Balloon Diameter (mm)
(atm) 1.50 2.00 2.25 2.50 2.75 3.00 3.25 3.50 3.75 4.00
4 1.40 1.79 2.00 2.21 2.43 2.65 2.88 3.11 3.31 3.51
5 1.45 1.85 2.07 2.29 2.52 2.75 2.99 3.23 3.44 3.66
6 1.50 1.91 2.14 2.36 2.62 2.87 3.10 3.33 3.55 3.78
7 1.55 1.96 2.20 2.44 2.69 2.94 3.18 3.41 3.66 3.91
8 1.58 2.00 2.25 2.50 2.75 3.00 3.25 3.50 3.75 4.00
9 1.61 2.04 2.29 2.55 2.80 3.06 3.31 3.56 3.82 4.08
10 1.63 2.07 2.33 2.59 2.84 3.10 3.36 3.62 3.88 4.15 Nominal pressure
11 1.66 2.10 2.36 2.62 2.89 3.15 3.41 3.66 3.94 4.21 Rated burst pressure*
12 1.68 2.12 2.39 2.66 2.92 3.18 3.44 3.71 3.99 4.26 *Rated burst pressuredo not exceed.
13 1.70 2.15 2.42 2.69 2.96 3.23 3.49 3.75 4.03 4.31
14 1.72 2.18 2.45 2.72 2.99 3.27 3.54 3.80 4.08 4.36 Nominal pressure: the pressure at
which the balloon reaches its labeled
15 1.75 2.20 2.47 2.74 3.03 3.32 3.59 3.86 4.14 4.42 diameter. Rated burst pressure: the
16 2.22 2.50 2.78 3.07 3.36 3.63 3.91 4.19 4.47 maximum pressure to which a balloon
17 2.25 2.53 2.81 3.10 3.40 3.68 3.96 4.24 4.52 is designed to be inflated (95% con-
fidence that 99.9% will not fail below
18 2.28 2.56 2.84 3.15 3.46 3.74 4.02 4.30 4.58 rated burst pressure).
TECHNICAL INFORMATION
Catheter length 138 cm Shaft dimensions for 1.53.5 mm
Gold-swaged marker bands Proximal 3.2 F
1.5 mm Single Distal 2.4 F/2.6 F
2.004.00 mm Double Shaft dimensions for 3.754.0 mm
Dura-Trac selective coating Proximal 3.2 F
Fulcrum balloon material Distal 2.5 F
MiniWrap MGCID 0.056"
1.5 mm 2 folds Test data on file at Medtronic, Inc.
2.03.75 mm 3 folds Bench test results may not be
4.0 mm 5 folds indicative of clinical performance.
13 For distribution in the USA only.

2011 Medtronic, inc. All rights reserved. UC200905056aen 7/11
CORONARY
Contents
NC Sprinter RX Noncompliant
Gold-swaged Proximal shaft
marker bands General Characteristics:
Supplied sterile.
items per box: 1
Dura-Trac
hydrophilic Soft Fulcrum Plus
Distal shaft coating balloon material
NC Sprinter RX Ordering Information

Diameter (mm) 6 9 12 15 21 27 O.D. mm (in.)
2.00 NCSP2006X NCSP2009X NCSP2012X NCSP2015X NCSP2021X 0.60 (0.024)
2.25 NCSP22506X NCSP22512X NCSP22521X 0.62 (0.024)
2.50 NCSP2506X NCSP2509X NCSP2512X NCSP2515X NCSP2521X NCSP2527X 0.63 (0.025)
2.75 NCSP27506X NCSP27512X NCSP27515X NCSP27521X 0.65 (0.025)
4.50 NCSP4515X NCSP4521X 0.76 (0.030)
5.00 NCSP5015X 0.80 (0.032)
NC Sprinter RX Compliance
Pressure Balloon Diameter (mm)
(atm) 2.00 2.25 2.50 2.75 3.00 3.25 3.50 3.75 4.00 4.50 5.00
8 1.98 2.17 2.45 2.70 2.97 3.09 3.36 3.62 3.87 4.27 4.75
9 2.00 2.20 2.49 2.74 3.01 3.15 3.42 3.68 3.93 4.34 4.84
10 2.02 2.23 2.51 2.77 3.04 3.18 3.45 3.72 3.97 4.39 4.91
11 2.03 2.24 2.53 2.80 3.07 3.22 3.49 3.76 4.01 4.44 4.97
12 2.05 2.26 2.55 2.82 3.10 3.25 3.52 3.79 4.05 4.48 5.01
13 2.07 2.28 2.57 2.84 3.13 3.28 3.55 3.82 4.08 4.51 5.06
14 2.08 2.30 2.58 2.87 3.15 3.31 3.58 3.85 4.11 4.55 5.10 Nominal pressure
15 2.10 2.32 2.60 2.89 3.18 3.33 3.61 3.88 4.15 4.58 5.14 Rated burst pressure*
16 2.12 2.33 2.62 2.91 3.20 3.36 3.63 3.90 4.18 4.61 5.18 *Rated burst pressuredo not exceed.
17 2.13 2.36 2.63 2.93 3.23 3.39 3.65 3.93 4.22 4.65 5.22
18 2.15 2.38 2.65 2.95 3.26 3.41 3.68 3.96 4.25 4.68 5.26 Nominal pressure: the pressure at
19 2.17 2.40 2.66 2.98 3.29 3.44 3.71 3.99 4.29 4.72 5.30 diameter. Rated burst pressure: the
20 2.19 2.42 2.68 3.00 3.47 3.73 4.02 4.76 maximum pressure to which a balloon
21 2.21 2.44 2.70 3.03 3.50 3.77 4.05 4.80 is designed to be inflated (95% con-
22 2.23 2.46 2.72 3.05 3.53 4.08 4.84 rated burst pressure).
Catheter length 142 cm Shaft dimensions for 4.005.00 mm
Gold-swaged marker bands Proximal 0.65 mm (1.9 F)
2.005.00 mm Double Distal 1.02 mm (3.0 F)
Dura-Trac selective coating MGCID 1.42 mm/.056" (2.004.00 mm)
Soft Fulcrum Plus balloon material MGCID 1.68 mm/0.066" (4.505.00 mm)
MiniWrap
2.003.75 mm 3 folds
4.005.00 mm 5 folds
Shaft dimensions for 2.003.75 mm
Proximal 0.65 mm (1.9 F) Test data on file at Medtronic, Inc.
Bench test results may not be
Distal 0.81 mm/0.86 mm (2.4 F/2.6 F) indicative of clinical performance.

CORONARY
Contents
NC Stormer OTw Noncompliant

Intermediate shaft Proximal shaft Tapered tip design
Supplied sterile.
Dura-Trac hydrophilic coating
items per box: 1
Fulcrum Plus balloon material

Distal shaft Swaged marker bands
NC Stormer OTw Ordering Information

Balloon Balloon Length (mm)
Diameter (mm) 6 11 14 16 18 21 26 31
2.00 NCS2006W NCS2011W NCS2016W NCS2021W
2.25 NCS22506W NCS22511W NCS22516W NCS22521W
2.50 NCS2506W NCS2511W NCS2514W NCS2516W NCS2518W NCS2521W NCS2531W
2.75 NCS27506W NCS27511W NCS27514W NCS27516W NCS27518W NCS27521W
3.00 NCS3006W NCS3011W NCS3014W NCS3016W NCS3018W NCS3021W NCS3026W NCS3031W
3.50 NCS3506W NCS3511W NCS3514W NCS3516W NCS3518W NCS3521W NCS3526W
NC Stormer OTw Compliance
Nominal pressure
Rated burst pressure*
*Rated burst pressuredo not exceed.
Nominal pressure: the pressure at

diameter. Rated burst pressure: the
maximum pressure to which a balloon
is designed to be inflated (95% con-
rated burst pressure).
Nominal pressure 2.04.0 mm 10 atm Dura-Trac selective coating
Rated burst pressure 2.04.0 mm 18 atm Soft Fulcrum Plus balloon material
Catheter length 138 cm No. of balloon folds
Distal/mid shaft O.D. 2.02.5 mm O.D.s 3 folds
Distal = 2.5 F Mid = 2.7 F Proximal = 3.2 F 2.753.0 mm O.D.s 4 folds
Exit markers 3.253.5 mm O.D.s 5 folds
Brachial, 88 cm Femoral, 98 cm 3.754.0 mm O.D.s 6 folds
Marker bands
2 on all 2.04.0 mm O.D.s
Bench test results may not be
indicative of clinical performance.

CORONARY
Contents
16
Contents
Coronary Guide Catheters
Supplied sterile.
Launcher Guide Catheters items per box: 1
LEFT CORONARY CURVES
Left
JL5.0
Standard JL3.0 JCL4.0
JL3.5 JL6.0
JCL4.5
JCL3.0
JL4.0
JCL3.5 JCL5.0
JL4.5
5F 6F 7F 8F
(i.D. 0.058 in.) (i.D. 0.071 in.) (i.D. 0.081 in.) (i.D. 0.090 in.)
Curve Style without Sideholes without Sideholes* without Sideholes* without Sideholes*
JL3.0 LA5JL30 LA6JL30 LA7JL30 LA8JL30
JCL3.0 LA5JCL30 LA6JCL30 LA7JCL30 LA8JCL30
Short
SL3.0
Left SL4.0 SL5.0
SL3.5 SL4.5 SL6.0
5F 6F 7F 8F
SL3.0 LA5SL30 LA6SL30 LA7SL30 LA8SL30
*To specify sideholes, add SH to the end of the product code.

17 2011 Medtronic, Inc. All rights reserved. UC200104300fEN 8/11
CORONARY
Guide Catheters
Contents
Launcher left coronary curves, continued
Amplatz
AL.75
Left AL2.0
AL3.0
AL1.0
AL1.5 AL2.5 AL4.0
5F 6F 7F 8F
AL.75 LA5AL75 LA6AL75 LA7AL75 LA8AL75
AL1.0 LA5AL10 LA6AL10 LA7AL10 LA8AL10
Short SAL.75
Amplatz SAL2.0 SAL3.0
Left SAL1.0
SAL1.5 SAL2.5 SAL4.0
5F 6F 7F 8F
SAL.75 LA5SAL75 LA6SAL75 LA7SAL75 LA8SAL75
SAL1.0 LA5SAL10 LA6SAL10 LA7SAL10 LA8SAL10
Left
Backup EBU3.0 EBU4.5
EBU3.75
Support
EBU EBU3.5 EBU4.0 EBU5.0

(Extra
Backup) 5F 6F 7F 8F
EBU3.0 LA5EBU30 LA6EBU30 LA7EBU30 LA8EBU30

CORONARY
Guide Catheters
Contents
Supplied sterile.
RIGHT CORONARY CURVES

Right JCR3.5
Standard JR3.0 JR4.5
JCR4.0
JR5.0
JR3.5
JCR4.5
JR6.0 JCR5.0
JR4.0
5F 6F 7F 8F
JR3.0 LA5JR30 LA6JR30 LA7JR30 LA8JR30
JCR3.5 LA5JCR35 LA6JCR35 LA7JCR35 LA8JCR35
Short Right SR3.0

SR4.0 SR5.0
SR6.0
SR3.5 SR4.5
5F 6F 7F 8F
SR3.0 LA5SR30 LA6SR30 LA7SR30 LA8SR30
SL6.0 LA5SR60 LA6SR60 LA7SR60 LA8SR60
AR1.0
Amplatz AR2.0 ALR1-2
Right
5F 6F 7F 8F
AR1.0 LA5AR10 LA6AR10 LA7AR10 LA8AR10
AR2.0 LA5AR20 LA6AR20 LA7AR20 LA8AR20
ALR1-2 LA5ALR12 LA6ALR12 LA7ALR12 LA8ALR12

Specialty curve for extra backup.

CORONARY
Guide Catheters
Contents
Launcher right coronary curves, continued
Short SAR1.0 SAR2.0

Amplatz
Right
5F 6F 7F 8F
SAR1.0 LA5SAR10 LA6SAR10 LA7SAR10 LA8SAR10
SAR2.0 LA5SAR20 LA6SAR20 LA7SAR20 LA8SAR20
Shepherds SCR3.5 SCR4.0 SCR5.0

Crook Right
5F 6F 7F 8F
SCR3.5 LA5SCR35 LA6SCR35 LA7SCR35 LA8SCR35
ECR ECR4.0 ECR4.5

ECR3.0
ECR3.5
5F 6F 7F 8F
ECR3.5 LA5ECR35 LA6ECR35 LA7ECR35 LA8ECR35
3DRC
Right
Backup RBU 3.5
RBU 4.5
Support 3DRIGHT
RBU 4.0 NOTO

RBU
NOTO
3DRC 5F 6F 7F 8F
3DRIGHT
RBU3.5 LA5RBU35 LA6RBU35 LA7RBU35 LA8RBU35
RBU4.0 LA5RBU40 LA6RBU40 LA7RBU40 LA8RBU40
RBU4.5 LA6RBU45
NOTO LA5NOTO LA6NOTO LA7NOTO LA8NOTO
3DRC LA63DRC LA73DRC LA83DRC
3DRIGHT LA53DRIGHT LA63DRIGHT

CORONARY
Guide Catheters
Contents
Supplied sterile.
items per box: 1
Launcher Guide Catheters
RADIAL CURVES
Radial Curves
MRADIAL RRAD
LARA
MRESS
5F 6F
(i.D. 0.058 in.) (i.D. 0.071 in.)
Curve Style without Sideholes without Sideholes
MRADIAL LA5MRADIAL LA6MRADIAL
MRESS LA5MRESS LA6MRESS
RRAD LA5RRAD LA6RRAD
LARA LA5LARA LA6LARA
Easy Radial erADL erADr erADrSt

easy radial Left easy radial right easy radial right Short tip
ERADL
erADLLt
easy radial Left Long tip
erADLSt
easy radial Left Short tip
5F 6F
Recommended Sizing (i.D. 0.058 in.) (i.D. 0.071 in.)
Curve Style Artery without Sideholes without Sideholes
ERADL Left main, standard-size aorta LA5ERADL LA6ERADL
ERADLLT Left main, enlarged aorta LA5ERADLLT LA6ERADLLT
ERADLST Left main, narrowed aorta LA5ERADLST LA6ERADLST
ERADR Right coronary artery, standard-size aorta LA5ERADR LA6ERADR
ERADRST Right coronary artery, narrowed aorta LA5ERADRST LA6ERADRST
Other Launcher 5F 6F 5F 6F
curves that can be (i.D. 0.058 in.) (i.D. 0.071 in.) (i.D. 0.058 in.) (i.D. 0.071 in.)
Curve Style without Sideholes without Sideholes Curve Style
used for without Sideholes without Sideholes
LA5EBU30 LA6EBU30 MAC3030 LA5MAC3030 LA6MAC3030
transradial LA5EBU35 LA6EBU35 LA5HSI LA6HSI
procedures LA5EBU375 LA6EBU375
EBU LA5HSII LA6HSII
LA5EBU40 LA6EBU40 HOCKEY STICK
LA5HSREL LA6HSREL
LA5EBU45 LA6EBU45 LA5HSIII LA6HSIII
LA5EBU50 LA6EBU50 MULTIPURPOSE LA5MPST LA6MPST
ALR12 LA5ALR12 LA6ALR12 IMA LA5IMA LA6IMA
LA5MAC30 LA6MAC30
LA5MAC35 LA6MAC35
MAC LA5MAC375 LA6MAC375
LA5MAC40 LA6MAC40
LA5MAC45 LA6MAC45

CORONARY
Guide Catheters
Contents
Supplied sterile.
OTHER CURVES
Multipurpose Hockey Stick Relaxed

MB1 MPST
MB2 Hockey Stick I Hockey Stick III
MP1
Hockey Stick II
MP2 El Gamal
5F 6F 7F 8F
MB1 LA5MB1 LA6MB1 LA7MB1 LA8MB1
MB2 LA5MB2 LA6MB2 LA7MB2 LA8MB2
MP1 LA5MP1 LA6MP1 LA7MP1 LA8MP1
MP2 LA6MP2
MPST LA5MPST LA6MPST LA7MPST LA8MPST
Hockey Stick I LA5HSI LA6HSI LA7HSI LA8HSI
Hockey Stick II LA5HSII LA6HSII LA7HSII LA8HSII
Hockey Stick Relaxed LA5HSREL LA6HSREL LA7HSREL LA8HSREL
Hockey Stick III LA5HSIII LA6HSIII LA7HSIII LA8HSIII
El Gamal LA5ELGAMAL LA6ELGAMAL LA7ELGAMAL LA8ELGAMAL
MAC
(Multi-Aortic) MAC3.0 MAC3.75 MAC4.5
MAC3.5 MAC4.0 MAC5.0
5F 6F 7F 8F
MAC3.0 LA5MAC30 LA6MAC30 LA7MAC30 LA8MAC30

CORONARY
Guide Catheters
Contents
Launcherother curves, continued
Bypass LCB
Curves
RCBII IMA
RCB
5F 6F 7F 8F
LCB LA5LCB LA6LCB LA7LCB LA8LCB
LCB (90 cm) LA7LCBD LA7LCBD LA8LCBD
RCB LA5RCB LA6RCB LA7RCB LA8RCB
RCB (90 cm) LA5RCBD LA6RCBD LA7RCBD LA8RCBD
RCBII LA5RCBII LA6RCBII LA7RCBII LA8RCBII
IMA LA5IMA LA6IMA LA7IMA LA8IMA
IMA (90 cm) LA5IMAD LA6IMAD LA7IMAD LA8IMAD
Champ Champ0.5
Champ2.0
Champ3.5
Champ1.0
Champ2.5
Champ4.0
Champ1.5 Champ3.0
5F 6F 7F 8F
Champ0.5 LA5CHAMP05 LA6CHAMP05 LA7CHAMP05 LA8CHAMP05

CORONARY
Guide Catheters
Contents

CORONARY
Guide Catheters
Contents
Supplied sterile.
items per box: 1
Sherpa NX Active Guide Catheters

Left
JL3.0 JL5.0 JCL4.0
Standard
JL3.5 JL6.0
JCL4.5
JCL3.0
JL4.0
JCL3.5 JCL5.0
JL4.5
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
Curve Style without Sideholes without Sideholes with Sideholes
JL3.0 SA5JL30 SA6JL30 SA6JL30SH
JCL3.0 SA5JCL30 SA6JCL30 SA6JCL30SH
Short Left SL3.0 SL4.0 SL5.0
SL3.5 SL4.5 SL6.0
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
SL3.0 SA5SL30 SA6SL30 SA6SL30SH

CORONARY
Guide Catheters
Contents
Sherpa nX Active left coronary curves, continued
Amplatz AL.75
Left AL2.0
AL3.0
AL1.0
AL1.5 AL2.5 AL4.0
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
AL.75 SA5AL75 SA6AL75 SA6AL75SH
AL1.0 SA5AL10 SA6AL10 SA6AL10SH
Short SAL.75
Left SAL1.0
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
SAL.75 SA5SAL75 SA6SAL75 SA6SAL75SH
SAL1.0 SA5SAL10 SA6SAL10 SA6SAL10SH
Left
EBU3.75
Support

(Extra Backup)
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
EBU3.0 SA5EBU30 SA6EBU30 SA6EBU30SH

CORONARY
Guide Catheters
Contents
Supplied sterile.
items per box: 1
Sherpa NX Active
Right JCR3.5
JR3.0 JR4.5
Standard
JCR4.0
JR5.0
JR3.5
JCR4.5
JR6.0 JCR5.0
JR4.0
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
JR3.0 SA5JR30 SA6JR30 SA6JR30SH
JCR3.5 SA5JCR35 SA6JCR35 SA6JCR35SH
Short Right SR3.0

SR4.0 SR5.0
SR6.0
SR3.5 SR4.5
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
SR3.0 SA5SR30 SA6SR30 SA6SR30SH
SL6.0 SA5SR60 SA6SR60 SA6SR60SH
Amplatz AR1.0 AR2.0 ALR1-2

Right
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
AR1.0 SA5AR10 SA6AR10 SA6AR10SH
AR2.0 SA5AR20 SA6AR20 SA6AR20SH
ALR1-2 SA5AR12 SA6ALR12 SA6ALR12SH

CORONARY
Guide Catheters
Contents
Sherpa nX Active right coronary curves, continued
Short SAR1.0 SAR2.0
Amplatz
Right
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
SAR1.0 SA5SAR10 SA6SAR10 SA6SAR10SH
SAR2.0 SA5SAR20 SA6SAR20 SA6SAR20SH

Crook Right
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
SCR3.5 SA5SCR35 SA6SCR35 SA6SCR35SH
Right
Backup ECR3.0 ECR4.0 ECR4.5
Support
ECR3.5
ECR
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
ECR3.0 SA6ECR30 SA6ECR30SH
ECR3.5 SA5ECR35 SA6ECR35 SA6ECR35SH
Backup 3DRIGHT
Support RBU 3.5

RBU 4.5
3DRC
RBU NOTO
RBU 4.0
NOTO
3DRC
3DRIGHT 5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
RBU3.5 SA5RBU35 SA6RBU35 SA6RBU35SH
RBU4.0 SA5RBU40 SA6RBU40 SA6RBU40SH
RBU4.5 SA6RBU45 SA6RBU45SH
NOTO SA5NOTO SA6NOTO SA6NOTOSH
3DRIGHT SA53DRIGHT SA63DRIGHT SA63DRIGHTSH
3DRC SA63DRC SA63DRCSH

CORONARY
Guide Catheters
Contents
Supplied sterile.
Sherpa NX Active items per box: 1
RADIAL CURVES
Radial Curves
MRADIAL RRAD
LARA
MRESS
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
Curve Style without Sideholes without Sideholes
MRADIAL SA5MRADIAL SA6MRADIAL
MRESS SA5MRESS SA6MRESS
RRADIAL SA5RRAD SA6RRAD
LARA SA5LARA SA6LARA

erADLLt
erADLSt
5F 6F
Recommended Sizing (i.D. 0.058 in.) (i.D. 0.070 in.)
Curve Style Artery without Sideholes without Sideholes
ERADL Left main, standard-size aorta SA5ERADL SA6ERADL
ERADLLT Left main, enlarged aorta SA5ERADLLT SA6ERADLLT
ERADLST Left main, narrowed aorta SA5ERADLST SA6ERADLST
ERADR Right coronary artery, standard-size aorta SA5ERADR SA6ERADR
ERADRST Right coronary artery, narrowed aorta SA5ERADRST SA6ERADRST
Other Sherpa NX 5F 6F 5F 6F
Active curves that
Curve Style without Sideholes without Sideholes Curve Style without Sideholes without Sideholes
can be used for SA5EBU30 SA6EBU30 MAC3030 SA5MAC3030 SA6MAC3030
transradial SA5EBU35 SA6EBU35 SA5HSI SA6HSI
procedures EBU
SA5EBU375 SA6EBU375 SA5HSII SA6HSII
SA5EBU40 SA6EBU40 HOCKEY STICK
SA5RMHSII SA6RMHSII
SA5EBU45 SA6EBU45 SA5HSIII SA6HSIII
SA5EBU50 SA6EBU50 MULTIPURPOSE SA5MPST SA6MPST
ALR12 SA5ALR12 SA6ALR12 IMA SA5IMA SA6IMA
SA5MAC30 SA6MAC30
SA5MAC35 SA6MAC35
MAC SA5MAC375 SA6MAC375
SA5MAC40 SA6MAC40
SA5MAC45 SA6MAC45

CORONARY
Guide Catheters
Contents
Supplied sterile.
items per box: 1
Sherpa NX Active
OTHER CURVES
Multipurpose Hockey Stick Relaxed
MB1 MPST
Hockey Stick III

Hockey Stick I
MB2
Hockey Stick II
MP1 El Gamal
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
MB1.0 SA5MB1 SA6MB1 SA6MB1SH
MB2.0 SA5MB2 SA6MB2 SA6MB2SH
MP1 SA5MP1 SA6MP1 SA6MP1SH
MP2 SA6MP2 SA6MP2SH
MPST SA5MPST SA6MPST
Hockey Stick I SA5HSI SA6HSI SA6HSISH
Hockey Stick II SA5HSII SA6HSII SA6HSIISH
Hockey Stick Relaxed SA5HSREL SA6HSREL SA6HSRELSH
Hockey Stick III SA5HSIII SA6HSIII SA6HSIIISH
El Gamal SA5ELGAMAL SA6ELGAMAL SA6ELGAMALSH
MAC
(Multi-Aortic)
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
MAC3.0 SA5MAC30 SA6MAC30 SA6MAC30SH

CORONARY
Guide Catheters
Contents
Sherpa nX Activeother curves, continued
Bypass
LCB
Curves
RCBII IMA
RCB
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
LCB SA5LCB SA6LCB SA6LCBSH
LCB (90 cm) SA6LCBD SA6LCBDSH
RCB SA5RCB SA6RCB SA6RCBSH
RCB (90 cm) SA5RCBD SA6RCBD SA6RCBDSH
RCBII SA5RCBII SA6RCBII SA6RCBIISH
IMA SA5IMA SA6IMA SA6IMASH
IMA (90 cm) SA5IMAD SA6IMAD SA6IMADSH
Champ Champ0.5
Champ2.0
Champ3.5
Champ1.0
Champ2.5
Champ4.0
Champ1.5 Champ3.0
5F 6F
(i.D. 0.058 in.) (i.D. 0.070 in.)
Champ0.5 SA5CHAMP05 SA6CHAMP05 SA6CHAMP05SH

CORONARY
Guide Catheters
Contents
Supplied sterile.
items per box: 1
Sherpa NX Balanced Guide Catheters

Left
JL3.0 JL5.0 JCL4.0
Standard
JL3.5 JL6.0
JCL4.5
JCL3.0
JL4.0
JCL3.5 JCL5.0
JL4.5
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
Curve Style without Sideholes* without Sideholes* without Sideholes*
JL3.0 SB6JL30 SB6JL30 SB6JL30
JCL3.0 SB6JCL30 SB6JCL30 SB6JCL30
Short SL3.0 SL4.0 SL5.0

Left
SL3.5 SL4.5 SL6.0
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
SL3.0 SB6SL30 SB7SL30 SB8SL30
*To specify sideholes, add SH to product code.

CORONARY
Guide Catheters
Contents
Sherpa nX Balanced left coronary curves, continued
Amplatz AL.75
AL2.0
Left AL3.0
AL1.0
AL1.5 AL2.5 AL4.0
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
AL.75 SB6AL75 SB7AL75 SB8AL75
AL1.0 SB6AL10 SB7AL10 SB8AL10
Short SAL.75
Left
SAL1.0
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
SAL.75 SB6SAL75 SB7SAL75 SB8SAL75
SAL1.0 SB6SAL10 SB7SAL10 SB8SAL10
Backup
Support EBU3.0 EBU3.75
EBU4.5
Left

(Extra
Backup) 6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
EBU3.0 SB6EBU30 SB7EBU30 SB8EBU30

CORONARY
Guide Catheters
Contents
Supplied sterile.
items per box: 1
Sherpa NX Balanced
Right JCR3.5
JR3.0 JR4.5
Standard
JCR4.0
JR5.0
JR3.5
JCR4.5
JR6.0 JCR5.0
JR4.0
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
JR3.0 SB6JR30 SB7JR30 SB8JR30
JCR3.5 SB6JCR35 SB7JCR35 SB8JCR35
Short Right SR3.0

SR4.0 SR5.0
SR6.0
SR3.5 SR4.5
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
SR3.0 SB6SR30 SB7SR30 SB8SR30
SL6.0 SB6SR60 SB7SR60 SB8SR60
Right
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
AR1.0 SB6SR30 SB7SR30 SB8SR30
AR2.0 SB6SR50 SB7SR50 SB8SR50
ALR1-2 SB6SR60 SB7SR60 SB8SR60

CORONARY
Guide Catheters
Contents
Sherpa nX Balanced right coronary curves, continued
Short AR1.0 AR2.0 ALR1-2
Amplatz
Right
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
SAR1.0 SB6SAR10 SB7SAR10 SB8SAR10
SAR2.0 SB6SAR20 SB7SAR20 SB8SAR20

Crook Right
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
SCR3.5 SB6SCR35 SB7SCR35 SB8SCR35
ECR
ECR4.0 ECR4.5
ECR3.0
ECR3.5
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
ECR3.0 SB7ECR30 SB8ECR30SH
ECR3.5 SB6ECR35 SB7ECR35 SB8ECR35SH
ECR4.0 SB6ECR40 SB7ECR40 SB8SCR40SH
ECR4.5 SB6ECR45 SB7ECR45 SB8ECR45SH
Right 3DRIGHT
Backup RBU 3.5

RBU 4.5
Support 3DRC
RBU 4.0 NOTO

RBU
NOTO
3DRC 6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
3DRIGHT
RBU3.5 SB6RBU35 SB7RBU35 SB8RBU35
NOTO SB6NOTO SB7NOTO SB8NOTO
3DRC SB73DRC SB83DRC
3DRIGHT SB63DRIGHT SB73DRIGHT SB83DRIGHT

CORONARY
Guide Catheters
Contents
Supplied sterile.
Sherpa NX Balanced items per box: 1
RADIAL CURVES
Radial Curves
MRADIAL RRAD
LARA
MRESS
6F 7F
(i.D. 0.070 in.) (i.D. 0.080 in.)
Curve Style without Sideholes without Sideholes*
MRADIAL SB6MRADIAL SB7MRADIAL
MRESS SB6MRESS SB7MRESS
RRAD SB6RRAD SB7RRAD
LARA SB6LARA SB7LARA

erADLLt
erADLSt
6F
Recommended Sizing (i.D. 0.070 in.)
Curve Style Artery without Sideholes
ERADL Left main, standard-size aorta SB6ERADL
ERADLLT Left main, enlarged aorta SB6ERADLLT
ERADLST Left main, narrowed aorta SB6ERADLST
ERADR Right coronary artery, standard-size aorta SB6ERADR
ERADRST Right coronary artery, narrowed aorta SB6ERADRST
Other Sherpa NX 6F *To specify sideholes,

6F
Balanced curves Curve (i.D. 0.070 in.) Curve
(i.D. 0.070 in.) add SH to product
that can be used for Style without Sideholes Style without Sideholes code.
transradial SA6EBU30 MAC3030 SA6MAC3030
procedures SA6EBU35 SA6HSI
SA6EBU375 SA6HSII
EBU HOCKEY STICK
SA6EBU40 SA6HSREL
SA6EBU45 SA6HSIII
SA6EBU50 MULTIPURPOSE SA6MPST
ALR12 SA6ALR12 IMA SA6IMA
SA6MAC30
SA6MAC35
MAC SA6MAC375 Sideholes available
SA6MAC40
SA6MAC45

CORONARY
Guide Catheters
Contents
Supplied sterile.
items per box: 1
Sherpa NX Balanced
OTHER CURVES
Multipurpose
Hockey Stick Relaxed
MB1 MPST
MB2 Hockey Stick I Hockey Stick III
MP1
Hockey Stick II
MP2 El Gamal
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
MB1 SB6MB1 SB7MB1 SB8MB1
MB2 SB6MB2 SB7MB2 SB8MB2
MP1 SB6MP1 SB7MP1 SB8MP1
MP2 SB6MP2
MPST SB6MPST SB7MPST SB8MPST
Hockey Stick I SB6HSI SB7HSI SB8HSI
Hockey Stick II SB6HSII SB7HSII SB8HSII
Hockey Stick Relaxed SB6RMHSII SB7RMHSII SB8RMHSII
Hockey Stick III SB6HSIII SB7HSIII SB8HSIII
El Gamal SB6ELGAMAL SB7ELGAMAL SB8ELGAMAL
MAC
(Multi-Aortic) MAC3.0 MAC4.5
MAC3.75
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
MAC3.0 SB6MAC30 SB7MAC30 SB8MAC30

CORONARY
Guide Catheters
Contents
Sherpa nX Balancedother curves, continued
Bypass LCB
Grafts
RCBII IMA
RCB
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
LCB SB6LCB SB7LCB SB8LCB
LCB (90 cm) SB6LCBD SB8LCBD
RCB SB6RCB SB7RCB SB8RCB
RCB (90 cm) SB6RCBD SB7RCBD SB8RCBD
RCBII SB6RCBII SB7RCBII SB8RCBII
IMA SB6IMA SB7IMA SB8IMA
IMA (90 cm) SB6IMAD SB7IMAD SB8IMAD
Champ Champ0.5
Champ2.0
Champ3.5
Champ1.0
Champ2.5
Champ4.0
Champ1.5 Champ3.0
6F 7F 8F
(i.D. 0.070 in.) (i.D. 0.080 in.) (i.D. 0.088 in.)
Champ0.5 SB6CHAMP05 SB7CHAMP05 SB8CHAMP05

CORONARY
Guide Catheters
Contents
Supplied sterile.
Z2 Guide Catheters items per box: 1

Left JL3.0 FL3.0 JCL3.0
Standard
FL3.5
JL3.5 JCL3.5
FL4.0
JL4.0
JCL4.0
FL4.5
JL4.5
JCL4.5
FL5.0
JL5.0
JCL5.0
FL6.0
JL6.0
5F 6F 7F 8F
JL3.0 ZM5JL30 Z26JL30 Z27JL30 Z28JL30
FL3.0 ZM5FL30 Z26FL30 Z27FL30 Z28FL30
JCL3.0 ZM5JCL30 Z26JCL30 Z27JCL30 Z28JCL30
Short
SL3.0 SL4.0 SL5.0
Left
SL3.5 SL4.5 SL6.0
5F 6F 7F 8F
SL3.0 ZM5SL30 Z26SL30 Z27SL30 Z28SL30

CORONARY
Guide Catheters
Contents
Z2 left coronary curves, continued
Amplatz AL.75
Left AL2.0
AL3.0
AL1.0
AL1.5 AL2.5 AL4.0
5F 6F 7F 8F
AL.75 ZM5AL75 Z26AL75 Z27AL75 Z28AL75
AL1.0 ZM5AL10 Z26AL10 Z27AL10 Z28AL10
Short SAL.75
Left SAL1.0
5F 6F 7F 8F
SAL.75 ZM5SAL75 Z26SAL75 Z27SAL75 Z28SAL75
SAL1.0 ZM5SAL10 Z26SAL10 Z27SAL10 Z28SAL10
Left
Support EBU3.75

(Extra
Backup) 5F 6F 7F 8F
EBU3.0 ZM5EBU30 Z26EBU30 Z27EBU30 Z28EBU30

CORONARY
Guide Catheters
Contents
Supplied sterile.
Right FR3.0 JCR3.5

JR3.0
Standard
FR3.5 JCR4.0
JR3.5
JR4.0 FR4.0
JCR4.5
JR4.5 FR4.5
JCR5.0
JR5.0 FR5.0
JR6.0
FR6.0
5F 6F 7F 8F
JR3.0 ZM5JR30 Z26JR30 Z27JR30 Z28JR30
FR3.0 ZM5FR30 Z26FR30 Z27FR30 Z28FR30
JCR3.5 ZM5JCR35 Z26JCR35 Z27JCR35 Z28JCR35
Short Right SR3.0

SR4.0 SR5.0
SR6.0
SR3.5 SR4.5
5F 6F 7F 8F
SR3.0 ZM5SR30 Z26SR30 Z27SR30 Z28SR30
SR4.5 Z26SR45 Z27SR45 Z28SR45
SL6.0 ZM5SR60 Z26SR60 Z27SR60 Z28SR60

CORONARY
Guide Catheters
Contents
Z2 right coronary curves, continued
AR1.0
Amplatz AR2.0
ALR1-2
Right
5F 6F 7F 8F
ALR1-2 is a specialty (i.D. 0.058 in.) (i.D. 0.070 in.) (i.D. 0.081 in.) (i.D. 0.091 in.)
curve for extra backup Curve Style without Sideholes without Sideholes* without Sideholes* without Sideholes*
AR1.0 ZM5AR10 Z26AR10 Z27AR10 Z28AR10
AR2.0 ZM5AR20 Z26AR20 Z27AR20 Z28AR20
ALR1-2 ZM5AR12 Z26AR12 Z27AR12 Z28AR12
SAR1.0 SAR2.0
Short
Amplatz
Right 5F 6F 7F 8F
SAR1.0 ZM5SAR10 Z26SAR10 Z27SAR10 Z28SAR10
SAR2.0 ZM5SAR20 Z26SAR20 Z27SAR20 Z28SAR20

Crook Right
5F 6F 7F 8F
SCR3.5 ZM5SCR35 Z26SCR35 Z27SCR35 Z28SCR35
ECR ECR4.0 ECR4.5

ECR3.0
ECR3.5
5F 6F 7F 8F
ECR3.5 Z26ECR35 Z27ECR35 Z28ECR35
ECR4.0 ZM5ECR40 Z26ECR40 Z27ECR40 Z28SCR40
ECR4.5 Z26ECR45 Z27ECR45 Z28ECR45
NOTO 3DRC
Right RBU3.5
Backup 3DRIGHT
Support RBU4.0
5F 6F 7F 8F
Curve Style without Sideholes without Sideholes without Sideholes without Sideholes
RBU35 Z26RBU35*
RBU40 Z26RBU40*
NOTO ZM5NOTO Z26NOTO* Z27NOTO* Z28NOTO*
3DRC Z263DRC
3DRIGHT ZM53DRIGHT Z263DRIGHT Z273DRIGHT

CORONARY
Guide Catheters
Contents
Supplied sterile.
OTHER CURVES
Multipurpose
Hockey Stick I Hockey Stick III
MB1
Hockey Stick II
MB2 El Gamal
Hockey Stick Relaxed

MP1
5F 6F 7F 8F
MB1 ZM5MB1 Z26MB1 Z27MB1 Z28MB1
MB2 ZM5MB2 Z26MB2 Z27MB2 Z28MB2
MP1 ZM5MP1 Z26MP1 Z27MP1 Z28MP1
MP2 Z26MP2
Hockey Stick I ZM5HSI Z26HSI Z27HSI Z28HSI
Hockey Stick II ZM5HSII Z26HSII Z27HSII Z28HSII
Hockey Stick Relaxed Z26RMHSII Z27RMHSII
Hockey Stick III ZM5HSIII Z26HSIII Z27HSIII Z28HSIII
El Gamal ZM5ELGAMAL Z26ELGAMAL Z27ELGAMAL Z28ELGAMAL
MAC
(Multi-Aortic) MAC3.0 MAC3.75 MAC4.5
5F 6F 7F 8F
MAC3.0 ZM5MAC30 Z26MAC30 Z27MAC30 Z28MAC30

Sidehole model not available.

CORONARY
Guide Catheters
Contents
Z2other curves, continued
Bypass RCB
LCB IMA
Curves
5F 6F 7F 8F
LCB ZM5LCB Z26LCB Z27LCB Z28LCB
LCB (90 cm) Z26LCBD Z27LCBD Z28LCBD
RCB ZM5RCB Z26RCB Z27RCB Z28RCB
RCB (90 cm) ZM5RCBD Z26RCBD Z27RCBD Z28RCBD
IMA ZM5IMA Z26IMA Z27IMA Z28IMA
IMA (90 cm) ZM5IMAD Z26IMAD Z27IMAD Z28IMAD
Champ Champ0.5
Champ2.0
Champ3.5
Champ1.0
Champ2.5
Champ4.0
Champ1.5 Champ3.0
5F 6F 7F 8F
Champ0.5 ZM5CHAMP05 Z26CHAMP05 Z27CHAMP05 Z28CHAMP05

CORONARY
Guide Catheters
Contents
Supplied sterile.
Zuma Guide Catheters items per box: 1

Left JL3.0 FL3.0 JCL3.0
Standard
FL3.5
JL3.5 JCL3.5
FL4.0
JL4.0
JCL4.0
FL4.5
JL4.5
JCL4.5
FL5.0
JL5.0
JCL5.0
FL6.0
JL6.0
7F
6F with radiopaque Marker Band 8F 9F
Curve Style without Sideholes* without Sideholes* without Sideholes* without Sideholes*
JL3.0 ZM6JL30 ZT7JL30 ZS8JL30 ZM9JL30
FL3.0 ZM6FL30 ZT7FL30 ZS8FL30 ZM9FL30
FL6.0 ZM6FL60 ZS8FL60 ZM9FL60
JCL3.0 ZM6JCL30 ZT7JCL30 ZS8JCL30 ZM9JCL30
Short SL3.0 SL4.0 SL5.0

Left
SL3.5 SL4.5 SL6.0
7F
SL3.0 ZM6SL30 ZT7SL30 ZS8SL30 ZM9SL30
SL6.0 ZM6SL60 ZT7SL60

CORONARY
Guide Catheters
Contents
Zuma left coronary curves, continued
Amplatz AL.75
AL2.0
Left AL3.0
AL1.0
AL1.5 AL2.5 AL4.0
7F
AL.75 ZM6AL75 ZT7AL75 ZS8AL75 ZM9AL75
AL1.0 ZM6AL10 ZT7AL10 ZS8AL10 ZM9AL10
Short SAL.75
Left SAL1.0
7F
SAL.75 ZM6SAL75 ZT7SAL75 ZS8SAL75 ZM9SAL75
SAL1.0 ZM6SAL10 ZT7SAL10 ZS8SAL10 ZM9SAL10
Left
EBU3.75
Support

(Extra
Backup) 7F
EBU3.0 ZM6EBU30 ZT7EBU30 ZS8EBU30 ZM9EBU30

CORONARY
Guide Catheters
Contents
Supplied sterile.
Zuma Guide Catheters items per box: 1

Right FR3.0 JCR3.5
JR3.0
Standard
FR3.5 JCR4.0
JR3.5
JR4.0 FR4.0
JCR4.5
JR4.5 FR4.5
JCR5.0
JR5.0 FR5.0
JR6.0
FR6.0
7F
JR3.0 ZM6JR30 ZT7JR30 ZS8JR30 ZM9JR30
FR3.0 ZM6FR30 ZT7FR30 ZS8FR30 ZM9FR30
JCR3.5 ZM6JCR35 ZT7JCR35 ZS8JCR35 ZM9JCR35
Short Right SR3.0

SR4.0 SR5.0
SR6.0
SR3.5 SR4.5
7F
SR3.0 ZM6SR30 ZT7SR30 ZS8SR30 ZM9SR30
SR4.5 ZS8SR45 ZM9SR45
SR6.0 ZM6SR60 ZT7SR60

CORONARY
Guide Catheters
Contents
Zuma right coronary curves, continued

Right
ALR1-2 is a specialty
curve for extra backup
7F
AR1.0 ZM6AR10 ZT7AR10 ZS8AR10 ZM9AR10
AR2.0 ZM6AR20 ZT7AR20 ZS8AR20 ZM9AR20
ALR1-2 ZM6ALR12 ZT7ALR12 ZS8ALR12 ZM9ALR12
Short SAR1.0 SAR2.0

Amplatz
Right
7F
Curve Style without Sideholes* with Sideholes without Sideholes* without Sideholes*
SAR1.0 ZM6SAR10 ZT7SAR10SH ZS8SAR10 ZM9SAR10
SAR2.0 ZM6SAR20 ZT7SAR20SH ZS8SAR20 ZM9SAR20
Shepherds
SCR3.5 SCR4.0 SCR5.0
Crook Right
7F
SCR3.5 ZM6SCR35 ZT7SCR35 ZS8SCR35 ZM9SCR35
Right NOTO 3DRIGHT
Backup
Support
7F
6F with radiopaque Marker Band 8F
(i.D. 0.068 in.) (i.D. 0.081 in.) (i.D. 0.091 in.)
NOTO ZM6NOTO ZT7NOTO ZS8NOTO
3DRIGHT ZM63DRIGHT

CORONARY
Guide Catheters
Contents
Supplied sterile.
items per box: 1
Zuma Guide Catheters
OTHER CURVES
Multipurpose
Hockey Stick III
MB1 Hockey Stick I
MB2
Hockey Stick II El Gamal

MP1
7F
MB1 ZM6MB1 ZT7MB1 ZS8MB1 ZM9MB1
MB2 ZM6MB2 ZT7MB2 ZS8MB2 ZM9MB2
MP1 ZT7MP1
Hockey Stick I ZM6HSI ZT7HSI ZS8HSI ZM9HSI
Hockey Stick II ZM6HSII ZT7HSII ZS8HSII ZM9HSII
Hockey Stick III ZM6HSIII ZT7HSIII ZS8HSIII ZM9HSIII
El Gamal ZM6ELGAMAL ZT7ELGAMAL ZS8ELGAMAL ZM9ELGAMAL
MAC
(Multi-Aortic)
7F
MAC3.0 ZM6MAC30 ZT7MAC30 ZS8MAC30 ZM9MAC30

CORONARY
Guide Catheters
Contents
Zumaother curves, continued
Bypass LCB RCB IMA

Curves
7F
LCB ZM6LCB ZT7LCB ZS8LCB ZM9LCB
LCB (90 cm) ZM6LCBD ZT7LCBD ZS8LCBD ZM9LCBD
RCB ZM6RCB ZT7RCB ZS8RCB ZM9RCB
RCB (90 cm) ZM6RCBD ZT7RCBD ZS8RCBD ZM9RCBD
IMA ZM6IMA ZT7IMA ZS8IMA ZM9IMA
IMA (90 cm) ZM6IMAD ZT7IMAD ZS8IMAD ZM9IMAD
Champ Champ0.5
Champ2.0
Champ3.5
Champ1.0
Champ2.5
Champ4.0
Champ1.5 Champ3.0
7F
Champ0.5 Z26CHAMP05 ZT7CHAMP05 ZS8CHAMP05 ZM9CHAMP05
Champ3.0 Z26CHAMP30 ZT7CHAMP30 ZS8CHAMP30

Contents
Embolic Protection
Supplied sterile.
includes two syringes, one filter and
Export AP Aspiration Catheter extension line with stopcock.
The Export AP Aspiration Catheter

uses a manual locking syringe
to easily remove embolic
material from throughout the
arterial system.
wire Compatibility
Product Code Guide/Sheath Compatibility (in.) Length (cm)
EXPORTAP 6 F min guide ID 0.070" 0.014 140
GEZ6200US7B 7 F min guide ID 0.080" 0.014 145
IMPORTANT INFORMATION: CAUTION: Federal (USA) law restricts these devices to sale by or on
Prior to use, refer to the Instructions for Use supplied with these the order of a licensed healthcare practitioner. See package inserts
devices for indications, contraindications, side effects, suggested for full product information.
procedure, warnings and precautions. Please consult your local Medtronic sales representative for more
information.
All brand names, product names or trademarks belong to their respective holders.
CORONARY
Embolic Protection
Contents
Supplied sterile. includes two
syringes, two filters and extension
Export XT Aspiration Catheter line with stopcock.
The Export XT Aspiration Catheter

uses a manual locking syringe to
easily remove embolic material from
throughout the arterial system.
wire Compatibility
Product Code Guide/Sheath Compatibility (in.) Length (cm)
EXPORTXT 6 F min guide ID 0.070" (5 F sheath) 0.014 140
GEZ6200US7B 6 F min guide ID 0.070" (5 F sheath) 0.014 145
Guardwire Temporary Occlusion and General Characteristics:

Supplied sterile.
Aspiration System items per box: 1
The GuardWire System utilizes an

atraumatic balloon to occlude
the vessel and prevent particu-
late debris from moving distally.
Intervention is performed over an
0.014" wire. The Export Aspiration
Catheter is then used to aspirate
the debris during balloon occlu-
sion. This simple, elegant solution
to distal protection has been clini-
cally proven to reduce cumulative
MACE events by 42 percent at
30-day follow-up when compared
with non-GuardWire procedures.*
* Donald S. Baim, on behalf of the

Saphenous vein graft Angioplasty Free Guardwire Total Length Balloon Occlusion Distal Tip
of Emboli Randomized (SAFER) trial Product Code wire O.D. (in.) (cm) Range (mm) Length (cm) Profile (in.)
investigators, Circulation 2002;105:1285- GEZ6200US 0.014 200 3.06.0 2.5 0.036
1290 GEZ6300US 0.014 300 3.06.0 2.5 0.036
GEZ5200US 0.014 200 2.55.0 2.5 0.028
GEZ5300US 0.014 300 2.55.0 2.5 0.028
IMPORTANT INFORMATION: CAUTION: Federal (USA) law restricts these devices to sale by or on
Prior to use, refer to the Instructions for Use supplied with these the order of a licensed healthcare practitioner. See package inserts
devices for indications, contraindications, side effects, suggested for full product information.
procedure, warnings and precautions. Please consult your local Medtronic sales representative for more
information.
Contents
Interventional Guidewires
Supplied sterile.
Zinger Stainless Steel workhorse Guidewire (0.014-in.) items per box: 5
The Zinger line of guidewires is the latest advancement in Zinger is available in various support levels as well as
highly trackable guidewires with excellent torque control. a marker version to meet your preference and clinical
Available with Pro/Pel silicone coating or Hydro-Track challenge.
hydrophilic coating for more treatment strategies. 2-cm radiopaque tip for visibility.
Zinger Light
Tip style: Forming ribbon
Outer coating: Hydro-Track
Product Product Code Tip Configuration Length (cm) Coating Comments
or Pro/Pel
Tip Stiffness Support ZINGER LS ZNGRLS180HS Straight tip 180 Hydro-Track DOC Compatible
ZINGER LS ZNGRLS180S Straight tip 180 Pro/Pel DOC Compatible
ZINGER LS ZNGRLS180HJ J-tip 180 Hydro-Track DOC Compatible
ZINGER LS ZNGRLS180J J-tip 180 Pro/Pel DOC Compatible
ZINGER LS ZNGRLS300HS Straight tip 300 Hydro-Track
ZINGER LS ZNGRLS300S Straight tip 300 Pro/Pel
ZINGER LS ZNGRLS300HJ J-tip 300 Hydro-Track
ZINGER LS ZNGRLS300J J-tip 300 Pro/Pel
Zinger Marker

Measuring zone 1 cm 1 cm 2 cm
or Pro/Pel
Tip Stiffness Support Product Product Code Tip Configuration Length (cm) Coating Comments
ZINGER MK ZNGRMK180HS Straight tip 180 Hydro-Track DOC Compatible
ZINGER MK ZNGRMK180S Straight tip 180 Pro/Pel DOC Compatible
ZINGER MK ZNGRMK180HJ J-tip 180 Hydro-Track DOC Compatible
ZINGER MK ZNGRMK180J J-tip 180 Pro/Pel DOC Compatible
ZINGER MK ZNGRMK300HS Straight tip 300 Hydro-Track
ZINGER MK ZNGRMK300S Straight tip 300 Pro/Pel
ZINGER MK ZNGRMK300HJ J-tip 300 Hydro-Track
ZINGER MK ZNGRMK300J J-tip 300 Pro/Pel
Zinger guidewires are continued on the next page
Important Information Potential Adverse Events:

Prior to use, refer to the Instructions for Use supplied with these devices for The following complications may be associated with the use of guide wire
indications, contraindications, side effects, suggested procedure, warnings and devices; excessive bleeding, air embolism, ischemia, hematoma at the puncture
precautions. site, infection, vessel spasm, vascular thrombosis and vessel dissection and
Indications for Use perforation.
Medtronic guide wires are steerable guide wires that are used for the introduc- CAUTION
tion and placement of diagnostic or interventional devices in the coronary Federal (USA) law restricts these devices to sale by or on the order of a licensed
and peripheral vasculature and may be used to reach and cross a target healthcare practitioner. See package inserts for full product information.
lesion. Medtronic guide wires are not intended for use in cerebral vasculature. Please contact your local Medtronic sales representative for more information.
Medtronic steerable exchange guide wires are used to facilitate the substitution
of one diagnostic or interventional device for another. Test data on file at Medtronic, Inc. Bench test results may not be indicative of
clinical performance.
53 2011 Medtronic, Inc. All rights reserved. UC200104301gEN 6/11
CORONARY
Contents
Supplied sterile.
items per box: 5
Zinger, continued
Zinger Medium
or Pro/Pel Product Product Code Tip Configuration Length (cm) Coating Comments
Tip Stiffness Support ZINGER MS ZNGRMS180HS Straight tip 180 Hydro-Track DOC Compatible
ZINGER MS ZNGRMS180S Straight tip 180 Pro/Pel DOC Compatible
ZINGER MS ZNGRMS180HJ J-tip 180 Hydro-Track DOC Compatible
ZINGER MS ZNGRMS180J J-tip 180 Pro/Pel DOC Compatible
ZINGER MS ZNGRMS300HS Straight tip 300 Hydro-Track
ZINGER MS ZNGRMS300S Straight tip 300 Pro/Pel
ZINGER MS ZNGRMS300HJ J-tip 300 Hydro-Track
ZINGER MS ZNGRMS300J J-tip 300 Pro/Pel
Zinger Support

Tip Stiffness Support ZINGER S ZNGRS190HS Straight tip 180 Hydro-Track DOC Compatible
ZINGER S ZNGRS190S Straight tip 180 Pro/Pel DOC Compatible
ZINGER S ZNGRS190HJ J-tip 180 Hydro-Track DOC Compatible
ZINGER S ZNGRS190J J-tip 180 Pro/Pel DOC Compatible
ZINGER S ZNGRS300HS Straight tip 300 Hydro-Track
ZINGER S ZNGRS300S Straight tip 300 Pro/Pel
ZINGER S ZNGRS300HJ J-tip 300 Hydro-Track
ZINGER S ZNGRS300J J-tip 300 Pro/Pel
CORONARY
Contents
Supplied sterile.
items per box: 5
Intuition Stainless Steel Advanced workhorse Guidewire (0.014-in.)

The Intuition Guidewire offers torque performance and Femoral (proximal) markers on wire, 90 cm and 100 cm
one-gram tip weight to give precision and confidence from distal tip.
during more difficult workhorse cases. Available with Pro/Pel silicone coating or Hydro-Track
Rounded tip and body provide control. hydrophilic coating for more treatment strategies.
Accu-Core technology provides torque performance to 3-cm radiopaque tip for visibility.
control and direct the wire.
Tip style: Core-to-tip

or Pro/Pel
Tip Stiffness Support
Intuition
3 cm

Intuition INTU180S Straight tip 180 Hydro-Track DOC Compatible
Intuition INTU180SS Straight tip 180 Pro/Pel DOC Compatible
Intuition INTU300S Straight tip 300 Hydro-Track
Intuition INTU300SS Straight tip 300 Pro/Pel
CORONARY
Contents
Supplied sterile.
items per box: 5
Cougar Nitinol workhorse Guidewire (0.014-in.)

The Cougar Steerable Guidewire offers the performance Available in Hydro-Track hydrophilic or Pro/Pel silicone
and support required for workhorse cases. coating.
Nitinol core wire. The Hydro-Track hydrophilic coating offers optimal
lubricity and durability.
Double coil tip design offers a soft tip with outstanding The Pro/Pel silicone coating offers traditional
tip shape retention. performance for situations that require reduced lubricity.
3-cm radiopaque tip for visibility.
Cougar LS
Light Support
Tip style: Forming ribbon 3 cm
Tip Stiffness Support COUGAR LS CGRLS190HS Straight tip 190 Hydro-Track DOC Compatible
COUGAR LS CGRLS190S Straight tip 190 Pro/Pel DOC Compatible
COUGAR LS CGRLS190HJ J-tip 190 Hydro-Track DOC Compatible
COUGAR LS CGRLS190J J-tip 190 Pro/Pel DOC Compatible
COUGAR LS CGRLS300HS Straight tip 300 Hydro-Track
COUGAR LS CGRLS300S Straight tip 300 Pro/Pel
COUGAR LS CGRLS300HJ J-tip 300 Hydro-Track
COUGAR LS CGRLS300J J-tip 300 Pro/Pel
Cougar XT
Medium Support

Outer coating: Hydro-Track Product Product Code Tip Configuration Length (cm) Coating Comments
or Pro/Pel COUGAR XT CGRXT190HS Straight tip 190 Hydro-Track DOC Compatible
COUGAR XT CGRXT190S Straight tip 190 Pro/Pel DOC Compatible
COUGAR XT CGRXT190HJ J-tip 190 Hydro-Track DOC Compatible
COUGAR XT CGRLS190J J-tip 190 Pro/Pel DOC Compatible
COUGAR XT CGRXT300HS Straight tip 300 Hydro-Track
COUGAR XT CGRXT300S Straight tip 300 Pro/Pel
COUGAR XT CGRXT300HJ J-tip 300 Hydro-Track
COUGAR XT CGRXT300J J-tip 300 Pro/Pel
CORONARY
Contents
Supplied sterile.
items per box: 5
Thunder Stainless Steel Extra-Support Guidewire (0.014-in.)

The Thunder Guidewire has a stainless steel core-to-tip Pro/Pel silicone coating.
design that provides enhanced support and stability while
3 cm radiopaque tip for visibility.
maintaining excellent torque characteristics with precise
tip control and steering.
Short transition zone (rail) provides support for accurate
device placement.

Outer coating: Pro/Pel
3 cm

THUNDER THNDR190S Straight tip 190 Pro/Pel DOC Compatible
THUNDER THNDR190J J Tip 190 Pro/Pel DOC Compatible
THUNDER THNDR300S Straight tip 300 Pro/Pel
THUNDER THNDR300J J Tip 300 Pro/Pel
CORONARY
Contents
Supplied sterile.
ProVia Stainless Steel Crossing Guidewire (0.014-in.) items per box: 5
The ProVia Crossing Guidewire is designed to cross demanding lesions. Femoral (proximal) markers on wire, 90 cm and 100 cm from distal tip.
Accu-Core wire technology is designed to provide torque performance to Available in Hydro-Track hydrophilic or Pro/Pel silicone coating.
control and direct the wire. The Hydro-Track hydrophilic coating offers optimal lubricity and durability.
Rounded tip and body provide control. The Pro/Pel silicone coating offers traditional performance for situations that
Tapered tip on ProVia 9 and 12 wires. require reduced lubricity.
1-mm noncoated tip on the hydrophilic version. 3-cm radiopaque tip for visibility.
ProVia 3
Straight tip (0.014 in.)
Tip style: Core-to-tip 3 cm

or Pro/Pel Product Product Code Size (g) Tip Configuration Length (cm) Coating Comments
Tip Stiffness Support ProVia 3 3PROV180HS 3 Straight tip 180 Hydro-Track DOC Compatible
ProVia 3 3PROV180SS 3 Straight tip 180 Pro/Pel DOC Compatible
ProVia 3 3PROV300HS 3 Straight tip 300 Hydro-Track
ProVia 3 3PROV300SS 3 Straight tip 300 Pro/Pel
ProVia 6
Straight tip (0.014 in.)

Tip Stiffness Support ProVia 6 6PROV180HS 6 Straight tip 180 Hydro-Track DOC Compatible
ProVia 6 6PROV180SS 6 Straight tip 180 Pro/Pel DOC Compatible
ProVia 6 6PROV300HS 6 Straight tip 300 Hydro-Track
ProVia 6 6PROV300SS 6 Straight tip 300 Pro/Pel
ProVia 9
Tapered tip (0.009 in.)

Tip Stiffness Support ProVia 9 9PROV180HS 9 Tapered tip 180 Hydro-Track DOC Compatible
ProVia 9 9PROV180SS 9 Tapered tip 180 Pro/Pel DOC Compatible
ProVia 9 9PROV300HS 9 Tapered tip 300 Hydro-Track
ProVia 9 9PROV300SS 9 Tapered tip 300 Pro/Pel
ProVia 12
Tapered tip (0.009 in.)

Tip Stiffness Support ProVia 12 12PROV180HS 12 Tapered tip 180 Hydro-Track DOC Compatible
ProVia 12 12PROV180SS 12 Tapered tip 180 Pro/Pel DOC Compatible
ProVia 12 12PROV300HS 12 Tapered tip 300 Hydro-Track
ProVia 12 12PROV300SS 12 Tapered tip 300 Pro/Pel
Contents
DIAGNOSTICS AND ACCESSORIES
Angiographic Catheters
Supplied sterile.
Color-coded luer and packaging.
SiteSeer Angiographic Catheters Maximum guidewire: 4 F = 0.035"
5/6 F = 0.038"
All curve styles have an atraumatic The unique coronary catheter shaft design incorporates The soft tip allows for gentle ostial intubation.
soft tip, with the exception of the a wire braid for responsive torque control and columnar SiteSeer catheters are engineered to withstand an
pigtail curves. XT shafts on 6 F strength. The polymer inner and outer jackets provide injection pressure of:
pigtails provide extra support for a large inner lumen for easy hand injection and clear 1195 psi: 6 F pigtail catheters
valve crossability. images. 1200 psi: All coronary and 5 F pigtail catheters
The ergonomic hub allows for comfortable catheter
manipulations and includes a color-coded luer for easy
size identification.
Pebax inner Strain ergonomic hub Color-coded

Catheter Construction Pebax
jacket relief luer
outer
5/6 F SiteSeer Catheters jacket
Double-braided
shaft
Inner Diameters
i.D. = 0.042" i.D. = 0.045" i.D. = 0.055" i.D. = 0.050"
4F 5F 6F 6F
Coronary and Coronary and Coronary catheters Pigtail catheters
pigtail catheters pigtail catheters
Straight Pigtail Product Code French Size Items per Box Sideholes Length (cm)
5A0069 5 10 6 110
5A0094 5 10 6 125
6A0031 6 10 6 110
6A0079 6 10 6 125
6A0028 6 10 12 110
6A0077 6 (XT) 10 6 110
6A0069 6 (XT) 10 12 110
6A0027 6 (XT) 10 6 125
Straight Tight Radius Pigtail Product Code French Size Items per Box Sideholes Length (cm)
4A0025 4 10 6 125
4A0028 4 10 6 110
5A0028 5 10 6 110
6A0092 6 (XT) 10 6 110
59 2011 Medtronic, Inc. All rights reserved. UC200104302eEN 11/11
CORONARY
Angiographic Catheters Contents
SiteSeer Angiographic Catheters, continued General Characteristics:

Supplied sterile.
All curve styles have an atraumatic soft tip, with the exception of the pigtail curves. Maximum guidewire: 4 F = 0.035"
XT shafts on 6 F pigtails provide extra support for valve crossability. 5/6 F = 0.038"
Van Tassel 145 Angled Product Code French Size Items per Box Sideholes Length (cm)
Pigtail 5A0070 5 10 6 110
6A0032 6 10 6 110
145 6A0029 6 10 12 110
6A0078 6 (XT) 10 6 110
6A0070 6 (XT) 10 12 110
Van Tassel 155 Product Code French Size Items per Box Sideholes Length (cm)
Angled Pigtail 5A0071 5 10 6 110
155
6A0030 6 10 12 110
6A0071 6 (XT) 10 12 110
145 Angled Product Code French Size Items per Box Sideholes Length (cm)
Tight Radius Pigtail 4A0026 4 10 6 125
4A0029 4 10 6 110
145
5A0029 5 10 6 110
6A0093 6 (XT) 10 6 110
155 Angled Product Code French Size Items per Box Sideholes Length (cm)
Tight Radius Pigtail 4A0027 4 10 6 125
155 4A0030 4 10 6 110
5A0030 5 10 6 110
Judkins Left 3.5 Product Code French Size Items per Box Length (cm)
5A0084 5 5 100
6A0080 6 5 100
Judkins Left 3.5 I Product Code French Size Items per Box Length (cm)
4A0010 4 5 100
5A0010 5 5 100
6A0010 6 5 100
CORONARY
Contents Angiographic Catheters

Supplied sterile.
5A0085 5 10 100
5A0089 5 10 125
6A0085 6 10 100
6A0087 6 10 125
4A0011 4 10 100
4A0040 4 10 125
5A0011 5 10 100
5A0040 5 10 125
6A0011 6 10 100
6A0042 6 10 125
5A0086 5 5 100
6A0082 6 5 100
Judkins Left 4.5 I Product Code French Size items per Box Length (cm)
4A0068 4 5 100
5A0060 5 5 100
6A0012 6 5 100
5A0087 5 5 100
6A0083 6 5 100
4A0012 4 5 100
5A0012 5 5 100
6A0013 6 5 100
4A0013 4 5 100
5A0013 5 5 100
6A0014 6 5 100
CORONARY

Supplied sterile.
No Torque Right Product Code French Size Items per Box Length (cm)
4A0006 4 5 100
5A0006 5 5 100
6A0006 6 5 100
3D Right Coronary Product Code French Size Items per Box Length (cm)
4A0007 4 5 100
5A0007 5 5 100
6A0007 6 5 100
Judkins Right 3.5 Product Code French Size Items per Box Length (cm)
4A0001 4 5 100
5A0001 5 5 100
6A0001 6 5 100
5A0002 5 10 100
5A0088 5 10 125
6A0002 6 10 100
6A0086 6 10 125
Judkins Right 4.0 I Product Code French Size Items per Box Length (cm)
4A0002 4 10 100
4A0041 4 10 125
5A0075 5 10 100
5A0041 5 10 125
6A0075 6 10 100
6A0043 6 10 125
Modified Judkins Right 4.0 Product Code French Size Items per Box Length (cm)
4A0003 4 10 100
5A0003 5 10 100
6A0003 6 10 100
4A0004 4 5 100
5A0004 5 5 100
6A0004 6 5 100
CORONARY

Supplied sterile.
4A0005 4 5 100
5A0005 5 5 100
6A0005 6 5 100
Amplatz Left I Product Code French Size Items per Box Length (cm)
4A0018 4 5 100
5A0018 5 5 100
6A0020 6 5 100
Amplatz Left II Product Code French Size Items per Box Length (cm)
4A0019 4 5 100
5A0019 5 5 100
6A0021 6 5 100
Amplatz Left III Product Code French Size Items per Box Length (cm)
4A0020 4 5 100
5A0020 5 5 100
6A0022 6 5 100
Amplatz Right I Product Code French Size Items per Box Length (cm)
4A0016 4 5 100
5A0016 5 5 100
6A0018 6 5 100
Modified Amplatz Right Product Code French Size Items per Box Length (cm)
4A0067 4 5 100
5A0068 5 5 100
6A0017 6 5 100
Amplatz Right II Product Code French Size Items per Box Length (cm)
4A0017 4 5 100
5A0017 5 5 100
6A0019 6 5 100
CORONARY

Supplied sterile.
Champ 0.5 Product Code French Size Items per Box Length (cm)
4A0008 4 5 100
4A0044 4 5 110
5A0008 5 5 100
5A0044 5 5 110
6A0008 6 5 100
6A0046 6 5 110
4A0009 4 5 100
5A0009 5 5 100
5A0045 5 5 110
6A0009 6 5 100
6A0047 6 5 110
5A0014 5 5 100
5A0046 5 5 110
6A0015 6 5 100
6A0048 6 5 110
5A0015 5 5 100
5A0047 5 5 110
6A0016 6 5 100
6A0049 6 5 110
Multipurpose A-1 Product Code French Size Items per Box Length (cm)
4A0021 4 5 100
4A0048 4 5 110
5A0021 5 5 100
5A0048 5 5 110
6A0023 6 5 100
6A0050 6 5 110
Multipurpose A-2 Product Code French Size Items per Box Length (cm)
(two sideholes) 4A0022 4 5 100
4A0049 4 5 110
5A0022 5 5 100
5A0049 5 5 110
6A0024 6 5 100
6A0051 6 5 110
CORONARY

Supplied sterile.
Multipurpose B-1 Product Code French Size Items per Box Length (cm)
4A0023 4 5 100
4A0050 4 5 110
5A0023 5 5 100
5A0050 5 5 110
6A0025 6 5 100
6A0052 6 5 110
Multipurpose B-2 Product Code French Size Items per Box Length (cm)
4A0051 4 5 110
5A0024 5 5 100
5A0051 5 5 110
6A0026 6 5 100
6A0053 6 5 110
Left Coronary Bypass Product Code French Size Items per Box Length (cm)
4A0032 4 5 100
5A0032 5 5 100
6A0034 6 5 100
Right Coronary Bypass Product Code French Size Items per Box Length (cm)
4A0033 4 5 100
5A0033 5 5 100
6A0035 6 5 100
Internal Mammary Artery Product Code French Size Items per Box Length (cm)
4A0031 4 5 100
5A0031 5 5 100
6A0033 6 5 100
Sones A Product Code French Size Items per Box Length (cm)
5A0055 5 5 80
5A0037 5 5 100
6A0057 6 5 80
6A0039 6 5 100
Sones B Product Code French Size Items per Box Length (cm)
5A0038 5 5 100
6A0058 6 5 80
6A0040 6 5 100
CORONARY
SiteSeer Angiographic Catheters General Characteristics:

Supplied sterile.
Sones C Product Code French Size Items per Box Length (cm)
6A0059 6 5 80
6A0041 6 5 100
Brachial 3.5 Product Code French Size Items per Box Length (cm)
(one sidehole) 4A0034 4 5 100
5A0052 5 5 80
5A0034 5 5 100
6A0054 6 5 80
6A0036 6 5 100
5A0053 5 5 80
5A0035 5 5 100
6A0055 6 5 80
6A0037 6 5 100
5A0036 5 5 100
6A0056 6 5 80
6A0038 6 5 100
Alternative Product Code Description French Size Items per Box Length (cm)
4A0042 Arani I 4 5 100
5A0042 Arani I 5 5 100

Arani l
6A0044 Arani I 6 5 100
6A0045 Arani II 6 5 100

Arani ll
5A0059 El Gamal I 5 5 100
6A0061 El Gamal I 6 5 100

El Gamal I
CORONARY
Supplied sterile.
Angio-Kits per box: 5
Maximum guidewire: see label
Packaging Options for SiteSeer Catheters Xt shafts on 6 F pigtails provide
extra support for valve crossability
Angio-Kits
Angio-Kit contains:
Judkins right
4-cm catheter
One Judkins Right 4-cm catheter (JR4.0)
Judkins Left i
One Judkins Left I 4-cm catheter (JL4.0 I) 4-cm catheter
One straight or angled pigtail catheter:
Straight Pigtail Catheter Product Code French Size Pigtail Curve Pigtail Sideholes
4A0061 4 Straight 6
5A0062 5 Straight 6
6A0063 6 Straight 12
6A0102 6 XT straight 6
145 Angled Pigtail Catheter Product Code French Size Pigtail Curve Pigtail Sideholes
4A0062 4 145 angle 6
5A0063 5 145 angle 6
145
6A0064 6 145 angle 12
6A0103 6 XT 145 angle 6
4A0063 4 155 angle 6
155
5A0064 5 155 angle 6
6A0065 6 155 angle 12
Angio-Kit contains:
One 3-D Right catheter
3-D right Catheter
One Judkins Left I 4-cm catheter (JL4.0 I)
Judkins Left i
One straight or angled pigtail catheter: 4-cm Catheter
4A0069 4 Straight 6
5A0072 5 Straight 6
145 Angled Pigtail Catheter
Product Code French Size Pigtail Curve Pigtail Sideholes

145 5A0095 5 145 angle 6
6A0108 6 XT 145 angle 6
CORONARY
Supplied sterile.

EZ-Pak Angiography Kits0.035" Guidewire
Angiography kit contains:

0.035" 3-mm J Standard taper Guidewire
One 0.035" 3-mm J 145-cm length
standard taper guidewire
Judkins right
One Judkins Right 4-cm catheter (JR4.0) 4-cm Catheter
Judkins Left i
4-cm Catheter
One Input PS introducer sheath

input PS introducer Sheath
One straight or angled pigtail
catheter:
Straight Pigtail Catheter

5A0065 5 Straight 6
5A0066 5 145 angle 6
145
6A0067 6 145 angle 12
6A0106 6 XT 145 angle 6
155 5A0067 5 155 angle 6
6A0068 6 155 angle 12

0.035 3-mm J Standard taper Guidewire
One 0.035" 3-mm J 145-cm-length
One 3-D Right catheter

Judkins Left i
3-D Right Catheter
One Judkins Left I 4-cm catheter (JL4.0 I) 4-cm Catheter
One straight pigtail catheter: input PS introducer Sheath
5A0073 5 Straight 6
CORONARY
Supplied sterile.
EZ-Pak Angiography Kit0.038" Guidewire

0.038" 3-mm J Standard taper Guidewire
standard taper guidewire Judkins right
4-cm Catheter
One Judkins Right 4-cm catheter (JR4.0) Judkins Left i
4-cm Catheter

input PS introducer Sheath
Straight Pigtail Catheter

5A0092 5 Straight 6
5A0093 5 145 angle 6
145 6A0101 6 145 angle 12
6A0107 6 XT 145 angle 6
CORONARY
Supplied sterile.
Color-coded strain relief and packaging.
Pro-Flo Angiographic Catheters Maximum guidewire: 0.038"

items per box: 10
Pro-Flo Standard Pro-Flo Soft Tip Pro-Flo XT Pro-Flo XT Soft Tip
The Pro-Flo catheter was designed Catheter ConstructionPro-Flo Standard and Pro-Flo with Soft Tip
with a high-strength polyurethane.
The wire braid assures a 1:1 torque
Winged Color- High-Strength
response. Hub Coded Polyurethane inner
Strain Core
relief
Polyurethane Wire Overbraid

Overjacket
Internal Diameters
i.D. = 0.050" i.D. = 0.061"
6 F Pro-Flo 7 F Pro-Flo
Pro-Flo Standard
Straight Pigtail Product Code French Size Tip Curve Style Sideholes Length (cm)
006803 6 Straight 6 110
006465 6 Straight 12 110
010245 7 Straight 6 110
010306 7 Straight 12 110
Van Tassel Angled Pigtail Product Code French Size Tip Curve Style Sideholes Length (cm)
006804 6 145 angled 6 110
145 Angled Pigtail 145 006896 6 145 angled 12 110
006897 6 155 angled 12 110
010246 7 145 angled 6 110
010307 7 145 angled 12 110
010308 7 155 angled 12 110
155 Angled Pigtail 155
Tight Radius Pigtail Product Code French Size Tip Curve Style Sideholes Length (cm)
060016 6 Straight TR 12 110
Straight tight radius Pigtail 060018 6 145 angled TR 12 110
145 Angled tight radius Pigtail

145
CORONARY
Supplied sterile.
Pro-Flo Standard Angiographic Catheters, continued Maximum guidewire: 0.038"
items per box: 10
Judkins Left Coronary Product Code French Size Tip Curve Length (cm) Length (cm)
006451 6 3.5 100
006452 6 4.0 100
060034 6 4.5 100
006453 6 5.0 100
010300 7 3.5 100
010301 7 4.0 100
010302 7 5.0 100
Judkins Right Coronary Product Code French Size Tip Curve Length (cm) Length (cm)
006454 6 3.5 100
006455 6 4.0 100
006456 6 5.0 100
010303 7 3.5 100
010304 7 4.0 100
010305 7 5.0 100
Amplatz Product Code French Size Tip Curve Style Length (cm)
006457 6 Right I 100
006458 6 Right II 100
Right l
006459 6 Left I 100
Right ll 006460 6 Left II 100
Left l 060039 6 Left III 100
010309 7 Right I 100
Left ll
010310 7 Right II 100
Left lll 010311 7 Left I 100
010312 7 Left II 100
Multipurpose Product Code French Size Tip Curve Style Length (cm)
006463 6 A-1 100
006464 6 A-2 100
A-1 010316 7 A-1 100
A-2 010317 7 A-2 110
Coronary Bypass Product Code French Size Tip Curve Style Length (cm)
006461 6 Left I 100
Left i
006462 6 Right I 100
010313 7 Left I 100
010314 7 Right I 100
right i
Internal Mammary Artery Product Code French Size Tip Curve Style Length (cm)
006470 6 IMA 100
iMA
010315 7 IMA 100
CORONARY
Supplied sterile.
Pro-Flo Soft Tip Angiographic Catheters Maximum guidewire: 0.038"
items per box: 10
Atraumatic tip, gradually tapering to 5.5 F. Catheter Construction Pro-Flo Soft Tip
Atraumatic
The Pro-Flo Soft Tip catheter features a soft tapered tip
Soft tip
Segment
tip designed to help reduce the risk of artery
dissection and vessel trauma.
With their unique configuration, Pro-Flo XT
catheters provide a stiffer shaft.
Internal Diameters
i.D. = 0.050" i.D. = 0.061"
010014 6 3.5 100
010015 6 4.0 100
060032 6 4.5 100
010016 6 5.0 100
010164 6 6.0 100
004910 7 3.5 100
004911 7 4.0 100
060050* 7 4.0* 100
060035 7 4.5 100
004912 7 5.0 100
004945 7 6.0 100
* Short Tip.
010017 6 3.5 100
010018 6 4.0 100
010019 6 5.0 100
010165 6 6.0 100
004913 7 3.5 100
004914 7 4.0 100
004915 7 5.0 100
004946 7 6.0 100
CORONARY
Pro-Flo Soft tip Angiographic Catheters, continued
010020 6 Right I 100
010021 6 Right II 100
Right l
004951 6 Modified Right 100
Right ll 010022 6 Left I 100
Left l 010023 6 Left II 100
Left ll
060046 6 Left III 100
004916 7 Right I 100
Left lll
004917 7 Right II 100
004925 7 Left I 100
004919 7 Left II 100
060040 7 Left III 100
010032 6 A-1 100
A-1
060047 6 A-1 125
010024 6 A-2 100
A-2 060042 6 A-2 125
010215 6 B-1 100
010216 6 B-2 100
B-1 004923 7 A-1 100
060044 7 A-2 125
004947 7 B-1 100
B-2
004948 7 B-2 100
Soft tip 010028 6 Left I 100
Left i 010030 6 Right I 100
004920 7 Left I 100
004921 7 Right I 100
right i
iMA 010026 6 IMA 100
004922 7 IMA 100
No Torque Right Coronary Product Code French Size Tip Curve Style Length (cm)
009228 6 No Torque Right 100
No Torque Right coronary catheters allow you to
engage the RCA without manipulation. 009229 7 No Torque Right 100
no torque right Coronary Catheter
CORONARY
Supplied sterile.
Pro-Flo XT Angiographic Catheter Maximum guidewire: 0.038"
items per box: 10
Atraumatic tip, gradually tapering to 5.5 F. Internal Diameters

The Pro-Flo Soft Tip catheter features a soft
tip designed to help reduce the risk of artery
dissection and vessel trauma. i.D. = 0.050" i.D. = 0.061"
With their unique configuration, Pro-Flo XT
catheters provide a stiffer shaft.
Straight Pigtail Product Code French Size Tip Curve Style Sideholes Length (cm)
010241 6 Straight 6 110
060048 6 Straight 6 125
010340 6 Straight 12 110
010243 7 Straight 6 110
010355 7 Straight 12 110
Van Tassel Angled Pigtail Product Code French Size Tip Curve Style Sideholes Length (cm)
010242 6 145 angled 6 110
010341 6 145 angled 12 110
060049 6 145 angled 6 125
010342 6 155 angled 12 110
010244 7 145 angled 6 110
010356 7 145 angled 12 110
010357 7 155 angled 12 110
Tight Radius Pigtail Product Code French Size Tip Curve Style Sideholes Length (cm)
Straight tight radius Pigtail 060017 6 Straight TR 12 110
060019 6 145 angled TR 12 110
145 Angled tight radius Pigtail

145
A-2 010321 6 A-2 110
010358 7 A-2 110
CORONARY
Supplied sterile.
Pro-Flo XT Soft Tip Angiographic Catheter Maximum guidewire: 0.038"
items per box: 10
The unique XT polymer overjacket is resistant Catheter Construction Pro-Flo Soft Tip
to softening at body temperature, an
Atraumatic Soft tip
important benefit in extended cases. tapered tip Segment
The Pro-Flo XT has the same internal diameter
and high flow rates as the standard Pro-Flo
catheters.
The Pro-Flo XT catheter features a soft tip
designed to help reduce the risk of artery
dissection and vessel trauma.
Internal Diameters
Atraumatic tip, gradually tapering to 5.5 F.
i.D. = 0.050" i.D. = 0.061"
010345 6 3.5 100
010343 6 4.0 100
060051 6 4.0 125
060033 6 4.5 100
010344 6 5.0 100
010160 6 6.0 100
010359 7 3.5 100
010360 7 4.0 100
060036 7 4.5 100
010361 7 5.0 100
010162 7 6.0 100
010319 6 3.5 100
010318 6 4.0 100
060052 6 4.0 125
010320 6 5.0 100
010161 6 6.0 100
010362 7 3.5 100
010363 7 4.0 100
010364 7 5.0 100
010163 7 6.0 100
010346 6 Right I 100
010347 6 Right II 100
Right l
010348 6 Left I 100
Right ll 010349 6 Left II 100
060038 6 Left III 100
Left l
010365 7 Right I 100
Left ll 010366 7 Right II 100
Left lll
010367 7 Left I 100
010368 7 Left II 100
CORONARY
Pro-Flo Xt Soft tip Angiographic Catheters, continued
010353 6 A-1 100
A-1
010354 6 A-2 110
010212 6 B-1 100
010213 6 B-2 100
A-2
010372 7 A-1 100
010373 7 A-2 110
B-1 010247 7 B-1 100
010248 7 B-2 100
B-2
010350 6 Left I 100
Left i 010351 6 Right I 100
010369 7 Left I 100
010370 7 Right I 100
right i
iMA 010352 6 IMA 100
010371 7 IMA 100
No Torque Right Coronary Product Code French Size Tip Curve Style Length (cm)
009234 6 No Torque Right 100
Product Description: 009235 7 No Torque Right 100
No Torque Right coronary catheters allow you to
engage the RCA without manipulation.
no torque right Coronary Catheter
CORONARY
Packaging Options for Pro-Flo Angiographic Catheters General Characteristics:

Supplied sterile.
Maximum guidewire: 0.038"
Angio-Kits Angio-Kits per box: 5
Angio-Kit contains:
One Judkins Left 4-cm catheter (JL4.0)

Judkins right
4-cm catheter
Judkins Left i
4-cm catheter
Straight Pigtail catheter Product Code French Size Design Style

008419 6 Pro-Flo
008420 6 Pro-Flo with soft tip
018418 6 Pro-Flo XT with soft tip
004901 7 Pro-Flo
145 Angled Pigtail catheter Product Code French Size Design Style
145
155
CORONARY
Supplied sterile.
Packaging Options for Pro-Flo Angiographic Catheters
EZ-Pak Angiography Kit contains:

0.035" 3-mm J standard taper guidewire

Judkins right
4-cm catheter

Judkins Left
4-cm catheter
input PS introducer sheath
Straight Pigtail catheter Product Code French Size Design Style

145 558445 6 Pro-Flo XT with soft tip
155 Angled Pigtail catheter

Product Code French Size Design Style
155
CORONARY
Supplied sterile.
Packaging Options for Pro-Flo Angiographic Catheters

EZ-Pak Angiography Kit contains:

0.038" 3-mm J standard taper guidewire
One 0.038" 3-mm J 145-cm length
Judkins right
One Judkins Right 4-cm catheter (JR4.0) 4-cm catheter
Judkins Left
4-cm catheter
One straight or angled pigtail input PS introducer sheath
catheter:
Straight Pigtail catheter


145 Angled Pigtail catheter
145
155
CORONARY
Supplied sterile.
Maximum guidewire:
7 F, 7.5 F and 8 F standard: 0.035"
Sones woven Coronary Catheters 7 F and 8 F Hi-Flow: 0.038"
items per box: 10
The Sones coronary catheter was developed Typical Sones Catheter Tip
with F. Mason Sones, MD, to meet the evolving
clinical needs of the brachial angiographer.
Two unique design features:
The woven core provides torque control.
The tapered tip adapts to anatomical 8 F shaft 1 in. 1.5 in. 5.5 F tip
taper length tip length
variations.
Medtronic supplies a variety of catheter
constructions and curve style tips as illustrated. Construction Styles
7 F Standard
Polyurethane buildup Woven core
Sones Hi-Flow
Polyurethane buildup Woven outer Wire nylon inner core

core braid (thin wall)
8 F Standard Nylon Core
Polyurethane buildup Woven outer nylon inner core

core
Sones Positrol Nylon Core
Polyurethane buildup Woven outer Wire braid nylon inner core

core
Sones Positrol woven Core
Polyurethane buildup Wire braid Woven inner core
CORONARY
Supplied sterile.
Maximum guidewire:
items per box: 10
Curve Style A
Standard Product Code French Size Length (cm) Tip Length (in.) Minimum Tip I.D. (in.) Comments
007764 7 80 1.5 0.036 Extra stiffnesstip & shaft
007536 7 100 1.5 0.036
Hi-Flow Product Code French Size Length (cm) Tip Length (in.) Minimum Tip I.D. (in.) Comments
All tips taper to 5.5 F.
008976 7 80 1.5 0.040
008977 7 100 1.5 0.040
008718 8 80 1.5 0.040
008971 8 100 1.5 0.040
Standard Nylon Core Product Code French Size Length (cm) Tip Length (in.) Minimum Tip I.D. (in.) Comments
007538 8 80 1.5 0.036
007539 8 100 1.5 0.036
007766 8 80 1.5 0.036 Extra stiffnesstip & shaft
007540 8 125 1.5 0.036
Positrol Nylon Core Product Code French Size Length (cm) Tip Length (in.) Minimum Tip I.D. (in.) Comments
008541 7.5 100 1.5 0.036 Extra stiffnessshaft
Curve Style B
1.0" (2.54 cm) curve length for normal aortic roots
Standard Product Code French Size Length (cm) Tip Length (in.) Minimum Tip I.D. (in.) Comments
007548 7 100 1.5 0.036
All tips taper to 5.5 F.
008978 7 80 1.5 0.040
008979 7 100 1.5 0.040
008719 8 80 1.5 0.040
007550 8 80 1.5 0.036
007551 8 100 1.5 0.036
Positrol woven Core Product Code French Size Length (cm) Tip Length (in.) Minimum Tip I.D. (in.) Comments
007561 7.5 80 1.5 0.036 Wire-reinforced
007562 7.5 100 1.5 0.036 Wire-reinforced
008554 7.5 100 1.5 0.036 Extra stiffnessshaft
CORONARY
Supplied sterile.
Maximum guidewire:
items per box: 10
Curve Style C
All tips taper to 5.5 F. 008980 7 80 1.5 0.040
008981 7 100 1.5 0.040
008720 8 80 1.5 0.040
008538 7.5 80 1.5 0.036
008539 7.5 100 1.5 0.036
008356 8 80 1.5 0.036 Standard nylon core
Brachial LTX-S Product Code French Size Length (cm) Tip Length (in.) Minimum Tip I.D. (in.) Comments
007770 8 80 Long tip 0.036
007771 8 100 Long tip 0.036
008358 8 80 1.5 0.036 Straight tip
008359 8 100 1.5 0.036 Straight tip
CORONARY
Supplied sterile.
items per box: 10 (Note: 5 per box for
Cardio-Marker image band models)
woven Coronary CathetersHigh-Volume
There are four high-volume angiographic catheters designed to facilitate large-volume contrast studies. The construction style
consists of a woven outer core and a polyurethane buildup with a smooth thromboresistant finish.
NIH Catheter Pediatric NIH Catheter Lehman Ventriculography Catheter Gensini Percutaneous Catheter
The NIH (National Institutes of Health) This thin-walled catheter is designed to J.S. Lehman, MD, developed the Lehman Goffredo G. Gensini, MD, is responsible for
catheter is designed with a thin wall provide maximum flow and flexibility. ventriculography catheter. This catheter is specifically the first designed catheter with an open end
and nylon core construction to provide The catheter can be used for aortic, designed to be placed easily into the left ventricle via the hole. This catheter has a tapered tip that fits
maximum flow rates and catheter stability. ventricular, pulmonary and large-vein aorta. The flexible, tapered distal tip is slightly curved to securely over a guidewire for percutaneous
The flexible tip makes positioning in contrast studies. assist passage through the aortic valve and to sit freely in introduction. The six sideholes and thin-wall
the cardiopulmonary system easier. This General Characteristics: the contour of the left ventricle. The location of the four construction provide maximum flow rates.
catheter is used to visualize the aorta,
Closed end sideholes enables the angiographer to record proximal The catheter is used for aortic, ventricular,
ventricles, pulmonary vasculature and the
Six sideholes (4 F catheter has four aortic pressures without removing the tip from the aortic pulmonary and large-venous contrast
great veins. sideholes) valve. This catheter provides excellent flow rates and studies.
Thin-wall construction catheter stability due to its thin-wall construction. General Characteristics:
General Characteristics: Open end
Nylon core General Characteristics:
Six sideholes
Closed end Closed end
Six sideholes Four sideholes Thin-wall construction
Thin-wall construction
NIH Product Code French Size Design Style Length (cm)

001348 5 Thin wall 50
001353 6 Thin wall 80
001358 7 Thin wall 100
001359 7 Thin wall 125
Pediatric NIH Product Code French Size Design Style Sideholes Length (cm)
001375 4 Thin wall 4 50
001377 5 Thin wall 6 50
001378 5 Thin wall 6 80
001380 6 Thin wall 6 50
001381 6 Thin wall 6 80
001382 6 Thin wall 6 100
Pediatric NIH with Cardio-Marker Product Code French Size Design Style Length (cm)
Image Bands 010010* 5 Thin wall 65
Bandwidth: 1 mm; two marker bands 1 cm 010011* 6 Thin wall 80
apart 0.5 mm (leading edge to leading edge)
010012* 7 Thin wall 80
*Items per box: 5
Pediatric Curved NIH Product Code French Size Design Style Length (cm)
008761 5 Thin wall 65
008762 6 Thin wall 65
008763 7 Thin wall 80
Lehman Ventriculography Product Code French Size Design Style Length (cm) Comments
001415 7 Thin wall 100 Closed end
Gensini Percutaneous Catheter French Minimum Tip Length

Product Code Size Design Style I.D. (in.) (cm) Comments
001323 5 Thin wall 0.026 100 Use with 0.025" guidewire
001339 6 Thin wall 0.036 80 Use with 0.035" guidewire
Pediatric product.
CORONARY
Supplied sterile.
items per box: 10
woven Coronary CathetersGeneral Purpose

and Transvalvular Catheters
The general construction of these catheters consists of a woven outer core and a high-density
polyurethane coating.
Cournand Catheter Lehman Catheter Goodale-Lubin Catheter

Designed by Andre Cournand, MD, in 1939, this J.S. Lehman, MD, designed a catheter for right heart Walter T. Goodale, MD, and Martin Lubin, MD,
catheter was the first to be manufactured specifically studies similar to the Cournand catheter. The Lehman developed standard-wall and thin-wall catheters
for use in the heart. The gradually curved tip facilitates catheter has a thin-wall construction that maximizes similar to the Cournand and Lehman catheters in
easy access to the right heart. The Cournand catheter flexibility and flow rates. construction and tip curve. The additional feature
catheter is used for blood sampling and pressure of the Goodale-Lubin catheter is the two laterally
measurements. opposed sideholes just proximal to the tip for
Open end improved disbursement of contrast during right heart
General Characteristics: No sideholes angiography.
Open end Thin-wall construction
No sideholes General Characteristics:
Standard wall construction Open end
Two laterally opposed sideholes
Thin-wall or standard-wall construction
Cournand Catheter Minimum Tip I.D.

Product Code French Size Design Style (in.) Length (cm)
001433 6 Standard wall 0.036 100
001434 6 Standard wall 0.036 125
007455 7 Standard wall 0.046 100
007456 7 Standard wall 0.046 125
Lehman Catheter Minimum Tip I.D.

001253 5 Thin wall 0.032 50
001254 5 Thin wall 0.032 80
001263 7 Thin wall 0.055 100
001264 7 Thin wall 0.055 125
Goodale-Lubin Catheter Minimum Tip I.D.

thin wall
001279 5 Thin wall 0.032 80
001453 5 Standard wall 0.026 50
001284 6 Thin wall 0.043 100
001288 7 Thin wall 0.055 100
Standard wall 007459 7 Standard wall 0.046 100
007460 7 Standard wall 0.046 125
Pediatric product.
Contents
Introducers
Supplied sterile.
items per box: 5
Input TS Introducer Sheaths
FEP sheath with silicone coating.
Silicone hemostasis valve. input tS introducer sheath dilator
Polyethylene dilator with
silicone coating. Double distal
J stainless steel guidewire
(included in 7-cm and 11-cm
sheaths only).
See obturators, dilators and input tS introducer sheath
sterile sleeves.
input tS introducer sheath with dilator
Input TS Introducer Obturator Length Dilator Length wire Style

Sheath Product Code French Size Included Color Code (cm) (cm) (in.)
040028A 5 No Gray 7 13 0.038 DDJ
040031A 6 No Green 7 13 0.038 DDJ
040035A 7 No Orange 7 13 0.038 DDJ
051101A 5 No Gray 11 17 0.038 DDJ
061101A 6 No Green 11 17 0.038 DDJ
071101A 7 No Orange 11 17 0.038 DDJ
081101A 8 No Blue 11 17 0.038 DDJ
091101A 9 No Gray 11 17 0.038 DDJ
010101A 10 No Dk Blue 11 17 0.038 DDJ
011101A 11 No Red 11 17 0.038 DDJ
060037A 6 Yes Green 23 29 N/A
070037A 7 Yes Orange 23 29 N/A
080037A 8 Yes Blue 23 29 N/A
090037A 9 Yes Gray 23 29 N/A
Input TS Introducer Obturator Length Dilator Length wire Style

Sheath with Needle and Product Code French Size Included Color Code (cm) (cm) (in.)
Guidewire 051102A 5 11 7 18 17 0.038 DDJ
061102A 6 11 7 18 17 0.038 DDJ
071102A 7 11 7 18 17 0.038 DDJ
081102A 8 11 7 18 17 0.038 DDJ
091102A 9 11 7 18 17 0.038 DDJ
Color Code for Introducer French Sizes

5F 6F 7F 8F 9F 10 F 11 F
CORONARY
Introducers Contents
Supplied sterile.
Input PS Introducer Sheaths items per box: 5
Pebax sheath.
Silicone hemostasis valve.
Polyethylene dilator.
Double distal J stainless steel.
guidewire (included in 11-cm
sheaths only). input PS introducer sheath
HydroPel hydrophilic coating:
water-activated, super lubricious
coating on the distal portions of
the sheath assembly.
See obturators, dilators, sterile
sleeves and Tuohy-Borst locking
device.
Input PS Introducer Obturator Length Dilator Length wire Style

Sheath Product Code French Size Included Color Code (cm) (cm) (in.)
050011 5 No Gray 11 17 0.038 DDJ
060011 6 No Green 11 17 0.038 DDJ
Available in Angio-Kits
070011 7 No Orange 11 17 0.038 DDJ
and EZ-Pak kits.
080011 8 No Blue 11 17 0.038 DDJ
090011 9 No Gray 11 17 0.038 DDJ
060023 6 Yes Green 23 31 N/A
070023 7 Yes Orange 23 39 N/A
080023 8 Yes Blue 23 39 N/A
090023 9 Yes Gray 23 39 N/A
853311 5 No Gray 11 17 N/A
863311 6 No Green 11 17 N/A
873311 7 No Orange 11 17 N/A
883311 8 No Blue 11 17 N/A
893311 9 No Gray 11 17 N/A
Input PS Introducer Length Needle Length Needle Dilator Length wire Style
Sheath with Needle and Product Code French Size (cm) (cm) Gauge (cm) (in.)
Guidewire 553311 5 11 7 18 17 Gray
563311 6 11 7 18 17 Green
573311 7 11 7 18 17 Orange
583311 8 11 7 18 17 Blue
593311 9 11 7 18 17 Gray
CORONARY
introducers
Contents Introducers
Supplied sterile.
items per box: 10
Input Accessories
Obturators Color-coded for easy identification of compatible sheath.

Helps maintain sheath patency and protects from outside
contamination. input introducer sheath short (11 cm)
obturator
TwistN Shut locking system locks obturator in place to prevent
backout from sheath.
Inserted into the introducer sheath when placement of the
transvenous temporary pacing electrode or intravascular catheter input introducer sheath long (23 cm)
is delayed or removed. obturator
Input PS Introducer Sheath Product Code Use with Introducer Obturator Included Obturator Length (cm) O.D. (in.)
Obturator 205211 050011 Gray 11 0.057
206211 060011 Green 11 0.065
207211 070011 Orange 11 0.078
208211 080011 Blue 11 0.091
209211 090011 Gray 11 0.104
206223 060023 Green 23 0.065
207223 070023 Orange 23 0.078
208223 080023 Blue 23 0.091
209223 090023 Gray 23 0.104
Input TS Introducer Product Code Use with Introducer Obturator Included Obturator Length (cm) O.D. (in.)
Sheath Obturator 205211A 051101A Gray 11 0.057
206211A 061101A Green 11 0.065
207211A 071101A Orange 11 0.078
208211A 081101A Blue 11 0.091
209211A 091101A Gray 11 0.104
206223A 060037A Green 11 0.065
207223A 070037A Orange 11 0.078
208223A 080037A Blue 11 0.091
209223A 090037A Gray 11 0.104
Vessel Dilators For use in arterial or venous

applications.
Polyethelyne dilator.
Input PS Introducer Product Code French Size Color Code Maximum wire Size (in.) Length (cm)
Sheath Vessel Dilator 653311 5 Gray 0.038 17
663311 6 Green 0.038 17
673311 7 Orange 0.038 17
683311 8 Blue 0.038 17
693311 9 Gray 0.038 17
663323 6 Green 0.038 31
673323 7 Orange 0.038 Double 39
683323 8 Blue 0.038 Double 39
693323 9 Gray 0.038 Double 39
Input TS Introducer Product Code French Size Color Code Maximum wire Size (in.) Length (cm)
Sheath Vessel Dilator 040037A 5 Gray 0.038 17
040042A 6 Green 0.038 17
040044A 7 Orange 0.038 17
040047A 8 Blue 0.038 17
040049A 9 Gray 0.038 17
Sterile Sleeves for Use with Input Introducer Sheaths

Maintains sterility of indwelling Product Code Length (cm)
catheter shaft proximal to the
026000 26
introducer hub.
060000 60 input introducer sheath sterile sleeve
Twist N Shut locking system locks
sleeve into input hub.
CORONARY
Supplied sterile.
Items per box: 10
Input SSV Split-Away Sheath

with Valve and Side Port
The Input SSV introducer
incorporates all the benefits of
a hemostasis valve into a split-
away sheath.
The Input SSV Introducer allows
you to exchange leads with Sheath length 13 cm
minimal blood loss. Dilator length 20 cm
Split-away sheath with
valve and side port
Sheath Length Dilator Length

Product Code French Size (cm) (cm)
808600 6 13 20
808700 7 13 20
808800 8 13 20
808900 9 13 20
808950 9.5 13 20
808100 10 13 20
808150 10.5 13 20
808110 11 13 20
808120 12 13 20
CORONARY
introducers
Contents Introducers
Supplied sterile.
items per box: 1
Transseptal Catheter Introducer Sheaths

Sets include one sheath and one
dilator. Use with Brockenbrough
needle, except where noted.
Mullins transseptal catheter introducer sheath
Mullins Transseptal Cath- Maximum wire Size Sheath Length Dilator Length
eter Introducer Sheath Product Code French Size (in.) (cm) (cm)
008550 6 0.032 59 67
008551 7 0.032 59 67
For use with Brockenbrough needle, 008552 8 0.032 59 67
product codes 003994 and 003993.
Mullins Transseptal Cath- Maximum wire Size Sheath Length Dilator Length
eter Introducer Sheath Product Code French Size (in.) (cm) (cm)
008530 6 0.025 44 52
Pediatric
008531 7 0.025 44 52
For use with pediatric Brockenbrough 008532 8 0.025 44 52
needle, product codes 003997 and
003996.
Pediatric product.
CORONARY
Supplied sterile.
items per box: 1
Transseptal Catheter Introducer

Sheath with Hemostasis Valve
Set includes one sheath and one

dilator. Used with Brockenbrough
needle.
Transseptal catheter introducer
sheath has attached sidearm with
stopcock and hemostasis valve.
For use with Brockenbrough needle, prod-

Maximum wire Size Sheath Length Dilator Length
uct code no. 003994.
Product Code French Size (in.) (cm) (cm)
008591 8 0.032 59 67
Contents
Interventional Accessories
Supplied sterile.
Everest Inflation Device items per box: 1

Kits per box: 1
Everest Inflation Device

Available with a three-way
stopcock.
The pistol-grip fits comfortably
in either hand.
A 20-cc syringe capacity
provides rapid negative
pressures to speed deflation
times.
The 20 atm/bar and 30 atm/bar
luminescent gauges are easy to Product Code Description Packaged with
read under normal and low-ight
conditions. AC2200 Everest20 inflation device 1 three-way stopcock
AC3200 Everest30 inflation device 1 three-way stopcock
Everest Survival Kit Product Code Description Packaged with
AC2205P Everest20 survival kit 1 Everest20 atm inflation device, 1 three-way stopcock,
Piton Y-adapter, guidewire insertion tool, and steering handle
AC3205P Everest30 survival kit 1 Everest30 atm inflation device, 1 three-way stopcock,
Piton Y-adapter, guidewire insertion tool, and steering handle
91 2011 Medtronic, Inc. All rights reserved. UC200104306dEN 9/11
CORONARY
Interventional Accessories Contents
Supplied sterile.
items per box: 5
Piton Disposable Adapters
Piton Y-Adapter
Package includes: Insertion tool
One Piton Y-Adapter
One insertion tool Piton Y-Adapter
Product Code Color Lumen I.D. (in.)

AC4001M Clear/Blue 0.110
Piton Y-Adapter Kit

Insertion tool
Kit includes:
One Piton Y-Adapter Piton Y-Adapter
One insertion tool

Steering handle
One steering handle
AC4003M 0.110
Piton Tri-Adapter
Package includes:
Insertion tool
One Piton Tri-Adapter
One insertion tool Piton Tri-Adapter

AC4002M 0.110
Stretch Insertion Tool

Stretch insertion tool for use with Piton Y-Adapter
and Piton Tri-Adapter.
Product Code
006073
Steering Handles
Steering Handle for Use with PTCA Product Code
Guidewires 008958
Plastic nut with metal jaws.
PTCA Guidewire Steering Handle

Also available kitted with Everest inflation device Product Code
and Piton Y-Adapters. AC4006
92 2011 Medtronic, Inc. All rights reserved. UC200104306dEN 9/11
Contents
Pediatric Products
Supplied sterile.
items per box: 10
Pediatric woven Coronary Catheters Maximum guidewire equals minimum
tip I.D.
The general construction of these catheters consists of a woven outer core and a high-density
polyurethane coating.
Lehman Catheter
J. S. Lehman, MD, designed the Lehman
ventriculography catheter. This catheter is specifically
designed to be placed easily into the left ventricle
via the aorta. The flexible, tapered distal tip is slightly French Minimum Tip I.D.
curved to assist passage through the aortic valve Product Code Size Design Style (in.) Sideholes Length (cm)
and to sit freely in the contour of the left ventricle. 001253 5 Thin wall 0.032 No sideholes 50
This catheter provides stability due to its thin-wall
construction. 001254 5 Thin wall 0.032 No sideholes 80
No sideholes
Goodale-Lubin Catheter
thin wall Standard wall
Walter T. Goodale, MD, and Martin Lubin, MD,
developed standard-wall and thin-wall catheters
similar to the Cournand and Lehman catheters in
construction and tip curve. The additional feature
of the Goodale-Lubin catheter is the two laterally French Minimum Tip I.D.
Product Code Size Design Style (in.) Sideholes Length (cm)
opposed sideholes just proximal to the tip for
improved disbursement of contrast during right heart 001279 5 Thin wall 0.032 2 80
angiography.
General Characteristics: 001453 5 Standard wall 0.026 2 50
Two laterally opposed sideholes
Thin-wall or standard-wall construction
Gensini Percutaneous Catheter

Goffredo G. Gensini, MD, is responsible for the first designed
catheter with an open-end hole. This catheter has a tapered French Minimum Tip Length
tip that fits securely over a guidewire for percutaneous Product Code Size Design Style I.D. (in.) Sideholes (cm) Comments
introduction. The six sideholes and thin-wall construction
provide maximum flow rates. The catheter is used for aortic, Use with 0.025"
001323 5 Thin wall 0.026 6 100
ventricular, pulmonary and large-venous contrast studies. guidewire
General Characteristics: Use with 0.035"
Open end 001339 6 Thin wall 0.036 6 80
guidewire
Six sideholes
Pediatric product.
CORONARY
Pediatric Products Contents
Supplied sterile.
items per box: 10 (Note: 5 per box for
Cardio-Marker Image Band models)
Maximum guidewire equals minimum
Pediatric woven NIH Catheters tip I.D.
High-volume angiographic catheters designed to facilitate large-volume contrast studies. The construction style
consists of a woven outer core and a polyurethane buildup with a smooth thromboresistant finish.
NIH
The NIH (National Institutes of Health) catheter is
designed with a thin wall and nylon core construction
to provide maximum flow rates and catheter stability.
The flexible tip makes positioning in the
cardiopulmonary system easier. This catheter is Product Code French Size Design Style Sideholes Length (cm)
used to visualize the aorta, ventricles, pulmonary 001348 5 Thin wall 6 50
vasculature and the great veins.
001353 6 Thin wall 6 80
Nylon core
Closed end
Six sideholes
Pediatric NIH Catheter

This thin-walled catheter is designed to provide
maximum flow and flexibility. The catheter can be Product Code French Size Design Style Sideholes Length (cm)
used for aortic, ventricular, pulmonary and large-vein
contrast studies. 001375 4 Thin wall 4 50
001377 5 Thin wall 6 50
001378 5 Thin wall 6 80
Nylon core
Closed end 001380 6 Thin wall 6 50
Six sideholes (4 F catheter has four sideholes) 001381 6 Thin wall 6 80
Thin-wall construction 001382 6 Thin wall 6 100
Pediatric Curved NIH

maximum flow and flexibility. The catheter can be
used for aortic, ventricular, pulmonary and large-vein
contrast studies.
Product Code French Size Design Style Sideholes Length (cm)
General Characteristics: 008761 5 Thin wall 6 65
Nylon core 008762 6 Thin wall 6 65
Closed end
Six sideholes 008763 7 Thin wall 6 80
Pediatric NIH with Cardio-Marker

Image Bands
maximum flow and flexibility. The catheter can be
used for aortic, ventricular, pulmonary and large-vein Product Code French Size Design Style Sideholes Length (cm)
contrast studies. 010010* 5 Thin wall 6 65
Bandwidth: 1 mm; two marker bands 2 cm 010011* 6 Thin wall 6 80
apart 0.5 mm (leading edge to leading edge)
010012* 7 Thin wall 6 80
*Items per box: 5
Pediatric product.
CORONARY
Contents Pediatric Products
Supplied sterile.
items per box: 1
Pediatric Rashkind Septostomy Balloon Catheters
Rashkind Balloon Cath-

eterSingle Lumen
Woven shaft design
Shaft length: 50 cm
Recommended Inflated Recommended

Product Code Shaft French Size Balloon Diameter (mm) Introducer (F) Comments
007161 4 11 7 Single lumen
007160 5 12 8 Single lumen
Rashkind Balloon Cath-

eterDouble Lumen
Woven shaft design
Shaft length: 50 cm
Recommended Inflated Recommended

Product Code Shaft French Size Balloon Diameter (mm) Introducer (F) Comments
007158 5.5 14 9 Double lumen
Pediatric product.
CORONARY
Pediatric Products Contents
not supplied sterile.
items per box: 1
Brockenbrough Needles
Brockenbrough needles and accessories are made of stainless steel.
The Brockenbrough needle is used with the Pediatric Mullins Transseptal Catheter Introducer
Sheath to perform the transseptal technique.
Brockenbrough
Curved Needle
To be used with the Pediatric Brockenbrough
Mullins Transseptal Catheter curved needle
Introducer Sheath. Product Code Size Length (cm)

003997 19 gauge 56
Brockenbrough
Needle Set
This needle set includes one
curved and one straight Brockenbrough straight needle Brockenbrough curved needle
needle.
The Brockenbrough needle Product Code Size Length (cm)
is used with the Pediatric 003996 19 gauge 56
Mullins Transseptal Catheter
Introducer Sheath.
Supplied sterile.
Maximum guidewire is 0.025"
Pediatric Mullins Transseptal Introducer Sheath items per box: 1
For use with pediatric

Brockenbrough needle,
product codes 003997 and
003996.
Set includes one sheath and
one dilator. Maximum wire Size Sheath Length Dilator Length
Product Code French Size (in.) (cm) (cm)
008530 6 0.025 44 52
008531 7 0.025 44 52
008532 8 0.025 44 52
Pediatric product.
Contents
Hemodynamic Monitoring Catheter
Supplied sterile.
For single use.
Pulmonary wedge Pressure (PwP) Catheter items per box: 5
Provides placement for

hemodynamic pressure
readings.
Large lumen for blood sampling Balloon inflation 1.5 cc
and pressure tracings.
Accommodates 0.038"
Product Code French Size Length (cm)
guidewire.
150075 7 110
Packaged with balloon inflation
syringe.
97 2011 Medtronic, Inc. All rights reserved. UC200104309cEN 9/11
CORONARY
Hemodynamic Monitoring Catheters Contents
Contents
Hemodynamic
AngiographicMonitoring
Guidewires Catheters
Supplied sterile.
Packaged in coiled hoops.
items per box: 10
Angiography guidewires are available in two core designs, fixed and movable: Fixed core
Fixed core: has a gradually tapered core.
Movable core: allows the wire softness to be adjusted manually by moving the
core wire back and forth, allowing the operator to lengthen or shorten at will.
Coatings: Angiography guidewires are available with a PTFE coating applied
Spring coil Core wire Safety wire
over the entire core, enabling free movement and a smooth sliding action. PTFE
wires are available with or without heparin coating. Movable core
Tips: A unique J Tip configuration is available on both the fixed and movable
core wires. This J Tip can be fingertip-straightened from virtually any point of
the wire shaft. This built-in convenience eliminates the need for a J straightening
tool for wire loading.
Medtronic offers a variety of tip configurations, sizes and styles. The two most
common tip configurations are straight and J.
Medtronic guidewires are available in a range of diameters and are compatible J Tip fixed core
with the following minimal needle sizes:
Safety wire
Guidewire Diameter (in./mm) Minimum Needle Size
0.025/0.6 19 gauge
0.032/0.8 18 gauge Spring coil Core wire
0.035/0.9 18 gauge
J Tip movable core
0.038/1.0 18 gauge
0.045/1.1 16 gauge
Handle
Stainless Steel Guidewires

Straight Tip: Fixed Core
Product Code Size (in./mm) Length (cm) Comments

007873 0.038/1.0 45 Standard taper core 6 cm
3-mm J Tip: Fixed Core

3-mm J Tip: Movable Core

008529 0.035/0.9 45 Double distal spring 3 cm
CORONARY
Angiographic Guidewires Contents
Supplied sterile.
items per box: 10
PTFE-Coated Guidewires: Fixed Core

007468 0.035/0.9 145 Extra-long taper core 15 cm
007467 0.035/0.9 145 Long taper core 10 cm
1.5-mm J Tip: Fixed Core

008944 0.035/0.9 175 Rosen guidewire
008945 0.038/1.0 175 Rosen guidewire



CORONARY
Contents Angiographic Guidewires
Supplied sterile.
items per box: 10
PTFE-Coated Guidewires: Movable Core
Straight Tip: Movable Core
Product Code Size (in./mm) Length (cm)

007647 0.032/0.8 145
007051 0.035/0.9 145
007053 0.038/1.0 145

007648 0.032/0.8 120
007649 0.032/0.8 145
007446 0.035/0.9 120
007447 0.035/0.9 145
007054 0.038/1.0 145

007445 0.035/0.9 145
Heparin over PTFE-Coated Guidewires (Fixed Core and Movable Core)



008441 0.035/0.9 145
008439 0.038/1.0 145
CORONARY
Supplied sterile.
Specialty Guidewires
3-mm J Tip Exchange
wire: Fixed Core
PTFE-coated.
Items per box: 10
Straight Tip Exchange

wire: Fixed Core
PTFE-coated. Product Code Size (in./mm) Length (cm) Comments
Items per box: 10 008633 0.035/0.9 260 Standard taper core 6 cm
PTFE-Coated 0.063"
Guidewire: Fixed Core
For placement of guiding catheter
(flexible distal tip).
PTFE-coated. Product Code Tip Diameter (in.) Length (cm)
Items per box: 1 008418 6 mm J 0.063 160
Sos Open-Ended Guide-

wire 6
Flow rate (cc / sec)
.038" OEGW
Movable/removable core wire is .035" OEGW
packaged with removable luer lock 4

hub, product code 006210 (shown
below). 2
Sos open-ended guidewire has a clear
PTFE outer jacket.
100 200 300 400 500 600
Items per box: 10 Pressure (PSi)

Removable Luer Lock

Hub
For use with Sos open-ended
guidewire (above). Product Code Size (in./mm) Comments
006210 Fits all sizes For use with Sos open-ended guidewire
CORONARY
Contents Angiographic Guidewires
Specialty Guidewires, continued General Characteristics:

Supplied sterile.
Steerable Guidewire
with Steering Handle
PtFe-coated.
items per box: 5
010037 0.035/0.9 145 3-cm flexible tip
010038 0.038/1.0 145 3-cm flexible tip
Softwire
PtFe-coated.
items per box: 10
Flexible tip

Steering Handle
PtFe-coated.
items per box: 5
Product Code Comments
006854 For use with 0.035"/0.038" guidewires
CORONARY
Contents
Transseptal Products
Brockenbrough Needles General Characteristics:

not supplied sterile.
Brockenbrough needles and accessories are made of stainless steel. items per box: 1
Brockenbrough
Curved Needle
The Brockenbrough needle is used
with one of the following transseptal
Brockenbrough
products to perform the transseptal curved needle
technique:
Mullins transseptal catheter Product Code Size Length (cm) Comments
introducer sheath
003994 18 gauge 71 To be used with either transseptal catheter introducer sheath
Transseptal catheter introducer
sheath To be used with the pediatric Mullins transseptal catheter
003997 19 gauge 56
introducer sheath
Brockenbrough
Needle Set
This needle set includes one curved
and one straight needle. Brockenbrough straight needle Brockenbrough curved needle
Product Code Size Length (cm) Comments

003993 18 gauge 71 To be used with either transseptal catheter introducer sheath
To be used with the pediatric Mullins transseptal catheter
003996 19 gauge 56
introducer sheath
Transseptal Catheter Introducer Sheaths General Characteristics:

Supplied sterile.
items per box: 1
needle, except where noted.
Mullins transseptal catheter introducer sheath
Mullins Transseptal Maximum wire Size Sheath Length Dilator Length

Catheter Introducer Product Code French Size (in.) (cm) (cm)
Sheath 008550 6 0.032 59 67
008551 7 0.032 59 67
For use with Brockenbrough
needle, product codes 003994 and 008552 8 0.032 59 67
003993.
Mullins Transseptal Maximum wire Size Sheath Length Dilator Length

Catheter Introducer Product Code French Size (in.) (cm) (cm)
008530 6 0.025 44 52
SheathsPediatric
008531 7 0.025 44 52
For use with Brockenbrough 008532 8 0.025 44 52
needle, product codes 003997
Pediatric product.
and 003996.
CORONARY
Transseptal Products Contents
Supplied sterile.
items per box: 1
Transseptal Catheter Introducer

Sheath with Hemostasis Valve

needle.
Transseptal catheter introducer sheath
has attached sidearm with stopcock
and hemostasis valve.
For use with Brockenbrough needle,

Product Code French Size Maximum wire Size (in.) Sheath Length (cm) Dilator Length (cm)
product code 003994.
008591 8 0.032 59 67
Contents
Contact and Ordering Information
Reimbursement Medtronics Healthcare Economics team is dedicated to educating customers on product coding, coverage
and reimbursement. It ensures that customers make economically efficient use of our products and submit
timely and accurate claims for services they perform. The Healthcare Economics Program provides a toll-free
coding hotline weekdays from 8 a.m. to 5 p.m. CST as well as web seminars on pertinent industry topics.
Vascular Reimbursement Information Line

Phone: 707.591.7869
Technical Support LifeLine Customer Support is a first point of contact for rapid turnaround to customers technical questions
and needs. Support services include expertise in objection handling, product specifications and use,
patient education and no cross.
For product information, contact:

LifeLine CardioVascular Technical Support
Phone: 877.526.7890
Alternate phone: 763.526.7890
Fax: 763.526.7888
Technical specialists are available weekdays from 7:30 a.m. to 6 p.m. CST.
Emergency service is available 24/7 outside of normal full-service hours.
Ordering To order products, contact:
Medtronic Product Services

Phone: 888.283.7868
Fax: 800.838.3103
Mailing address:
Medtronic, Inc.
CardioVascular Customer Care
800 - 53rd Ave. NE
Columbia Heights, MN 55421
Customer Care specialists are available weekdays from 7 a.m. to 7 p.m. CST.
Emergency service is available outside of normal full-service hours.
Shipping Medtronic will incur all shipping charges. Standard delivery is ground, but shipping can be upgraded upon
request. If product is damaged in shipment, obtain a claim inspection report from the carrier within 15 days.
Pricing and Terms Prices are subject to change without prior notice. Payment is required within net 30 days of invoice. Please
contact Customer Care for questions regarding remittance for your ZIP code.
Return Policy Authorization must be obtained from your Medtronic sales representative or Customer Care specialist
before product is returned. Please be prepared with the reason for return, model, lot number, quantity and
original purchase order (PO). The Returned Goods Authorization (RGA) number must be clearly identified
on the carton of returned product. Product may be subject to a 20% restocking fee. Merchandise processed
in error by Medtronic will be credited in full.
Note: Product availability and specifications are subject to change without notice.
107
Contents
Contact and Ordering information, continued
Product Eligible Product must be:

for Return Within 90 days of invoice.
In unopened, saleable condition.
An active model included in the current price list.
A product that has not reached or exceeded the use-before date.
A complete box or kit.
A standard catalog item (special build product is not eligible for return).
Shipping Address Medtronic Inc. (RGA#)

for Returns Attn: Return Finished Goods
4340 Swinea Road, Building A
Memphis, TN 38118
Note: Product availability and specifications are subject to change without notice.
August 2011
108
2011 Coronary Diagnostic and Intervention Coding Sheet
Patient Name Date of Birth Date of Procedure CardioVascular Reim-
bursement Information
Referring MD Dx Line
Tel: 707.591.7869
DIAGNOSTIC (NONCONGENITAL) ADDITIONAL PROCEDURES

Right heart catheterization, including measurements when performed 93451 Intravascular ultrasound (coronary vessel or graft), initial vessel 92978 (+)
Left heart catheterization, including left ventriculography when performed 93452 Intravascular ultrasound (coronary vessel or graft), each additional vessel 92979 (+)
Combined left and right heart catheterization including left ventriculography when performed 93453 Left heart catheterization by transseptal puncture 93462 (+)
Coronary angiography only without left or right heart catheterization 93454 Pharmacologic agent administration including hemodynamic measurements* 93463 (+)
Coronary angiography without left or right heart cath, with angiography of bypass graft(s) 93455 Physiologic exercise study including hemodynamic measurements 93464 (+)
Coronary angiography with right heart cath 93456 Insertion and placement of flow directed catheter for monitoring purposes (Swan-Ganz) 93503
Coronary angiography with angiography of bypass graft(s) and right heart cath 93457 Endomyocardial biopsy 93505
Coronary angiography with left heart cath, including left ventriculography when performed 93458 Indicator dilution studies including arterial and/or venous catheterization, with cardiac output measurement 93561
Coronary angiography with left heart cath with angiography of bypass graft(s) including left ventriculography 93459 (separate procedure)
when performed Indicator dilution studies, subsequent measurement of cardiac output 93562
Coronary angiography with left and right heart cath, including left ventriculography when performed 93460 Intravascular distal blood flow velocity and/or pressure derived coronary flow reserve measurement, during 93571 (+)
Coronary angiography with left and right heart cath, with angiography of bypass graft(s) including left 93461 coronary angiography, initial vessel
ventriculography when performed Intravascular distal blood flow velocity and/or pressure derived coronary flow reserve measurement, during 93572 (+)
RULES coronary angiography, each additional vessel
All new bundled diagnostic codes, with the exception of right heart cath 93451, include catheter placement, injection and Renal angiography, nonselective, one or both kidneys, during cardiac cath or coronary angiography G0275
supervision & interpretation.
Iliac and/or femoral artery angiography, nonselective, bilateral or ipsilateral to cath insertion during cardiac G0278
cath or coronary angiography
DIAGNOSTIC CONGENITAL
Right heart catheterization, for congenital cardiac anomalies RULES
93530
* Report 93463 only once per left or right heart cath procedure. Do not report with coronary interventions.
Combined right heart catheterization and retrograde left heart catheterization, for congenital cardiac
anomalies 93531
INTERVENTIONS
Combined right heart catheterization and transseptal left heart catheterization through intact septum with or
93532 Percutaneous transluminal coronary thrombectomy 92973 (+)
without retrograde left heart catheterization, for congenital cardiac anomalies
Transcatheter placement of radiation delivery device for subsequent coronary intravascular brachytherapy 92974 (+)
Combined right heart catheterization and transseptal left heart catheterization through existing septal open-
ing, with or without retrograde left heart catheterization, for congenital cardiac anomalies 93533 Thrombolysis, coronary; by intracoronary infusion, including selective coronary angiography 92975
Injection procedure, including S&I, for selective coronary angiography during CONGENITAL heart cath 93563 (+) Transcatheter placement of an intracoronary stent(s), percutaneous, with or without other therapeutic 92980
intervention, any method; single vessel
Injection procedure, including S&I, for selective angiography of venous or arterial bypass graft(s) during
CONGENITAL cath 93564 (+) Transcatheter placement of an intracoronary stent(s), percutaneous, with or without other therapeutic 92981 (+)
intervention, any method; each additional vessel
Injection procedure, including S&I, for selective left ventricular or left atrial angiography during CONGENITAL
heart cath 93565 (+) Transcatheter placement of a drug eluting intracoronary stent(s), percutaneous, with or without other thera- G0290
RULES
peutic intervention, any method; single vessel*
Anomalous coronary arteries, PFO, MVP, and bicuspid aortic valve are not considered congenital cardiac anomalies for coding Transcatheter placement of a drug eluting intracoronary stent(s), percutaneous, with or without other thera- G0291
purposes and are assigned to the regular diagnostic codes 93451-93461. peutic intervention, any method; each additional vessel*
Percutaneous transluminal coronary balloon angioplasty; single vessel 92982
ADDITIONAL INJECTIONS Percutaneous transluminal coronary balloon angioplasty; each additional vessel 92984 (+)
Injection procedure for selective right ventricular or right atrial angiography 93566 (+) Percutaneous transluminal coronary atherectomy, by mechanical or other method, with or without balloon 92995
Injection procedure for supravalvular aortography 93567 (+) angioplasty; single vessel
Injection procedure for pulmonary angiography 93568 (+) Percutaneous transluminal coronary atherectomy, by mechanical or other method, with or without balloon 92996 (+)
RULES angioplasty; each additional vessel
These injection codes can be added on to both the regular diagnostic catheterization codes and to the congenital catheterization codes. Percutaneous transluminal pulmonary artery balloon angioplasty; single vessel 92997
Percutaneous transluminal pulmonary artery balloon angioplasty; each additional vessel 92998(+)
MISCELLANEOUS
RULES
Conscious sedation 99143-99150 * For insertion of drug-eluting stents, Medicare requires hospitals to use codes G0290 and G0291. Hospitals use 92980 and 92981 for non-drug-
Closure device G0269 eluting stents only. However, physicians continue to use 92980 and 92981 for both drug-eluting and non-drug-eluting stents.
Medtronic may not carry products used in all procedures listed. 2011 Medtronic, Inc. All rights reserved. Printed in USA. UC201104888EN 2/11
Contents
For distribution in the USA only. 2012 Medtronic, inc. All rights reserved. Printed in USA. UC200805154cen 2/12
For further information, please call and/or consult Medtronic

at the toll-free numbers or websites listed below:
www.medtronic.com
www.medtronicstents.com
Medtronic, Inc. LifeLine Customer Support
3576 Unocal Place Tel: 877.526.7890
Santa Rosa, CA 95403 Tel: 763.526.7890
USA
Tel: 707.525.0111 Product Services
Tel: 888.283.7868 CAUTION: Federal (USA) law restricts these devices to sale by
Fax: 800.838.3103 or on the order of a licensed healthcare practitioner.

2012 Medtronic Coronary Catalog

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Contents

At Medtronic, were committed to innovating for life by pushing the

Through continued innovation and collaboration, we are pleased to offer one

(continued on next page)

Diagnostics and Accessories

Contact and Ordering Information

Contact and Ordering information . . . . . . . . . . . . . . . . . . . . . 107

Drug-Eluting Coronary Stents

Resolute Integrity Drug-Eluting

Resolute Integrity DES, built on

Resolute Integrity RX Ordering Information

Resolute Integrity RX Compliance

For distribution in the USA only.

For distribution in the USA only.

Resolute Integrity Drug-Eluting

1.1 mm (3.4 F) Minimal balloon

Resolute Integrity OTw Ordering Information

Resolute Integrity OTw Compliance

For distribution in the USA only.

For distribution in the USA only.

Endeavor Sprint Zotarolimus-Eluting

Endeavor Sprint RX Compliance

5 2009 Medtronic, inc. All rights reserved. UC200904590en 3/09

Endeavor Sprint Zotarolimus-Eluting

Endeavor Sprint OTw Compliance

6 2009 Medtronic, inc. All rights reserved. UC200904589en 3/09

Bare Metal Coronary Stents

Integrity RX Coronary Stent System

The Integrity bare metal coronary

Integrity RX Ordering Information

For distribution in the USA only.

For distribution in the USA only.

Integrity OTw Coronary Stent System General Characteristics:

1.1 mm (3.4 F) Minimal balloon

Integrity OTw Ordering Information

Integrity OTw Compliance

For distribution in the USA only.

For distribution in the USA only.

Balloon Dilatation Catheters

Sprinter Legend Semicompliant Balloon Dilatation Catheter

Sprinter Legend OTW Ordering Information

Compatible with 6 F Technical Information

For distribution in the USA only.

Sprinter Legend 1.25 mm Semicompliant

Flexible FasTrac tip design Product Description:

Sprinter Legend 1.25 mm OTw Ordering Information

Sprinter Legend 1.25 Compliance

7 0.67 1.25 mm Zerofold

The Lowest Crossing Profile on the Market

SuperCrosser Zerofold Technology 0.5-mm (0.020")

Micro-Brite 0.41-mm (0.016")

* Medtronic CardioVascular in Ireland was selected as the overall winner of the

For distribution in the USA only.

Sprinter OTw Semicompliant

Flexible FasTrac tip

Sprinter OTw Ordering Information

Sprinter OTw Compliance

13 For distribution in the USA only.

Flexible FasTrac tip

NC Sprinter RX Ordering Information