Cadd Legacy One 6400
Cadd Legacy One 6400
Cadd Legacy One 6400
CADD-Legacy 1
CONTINUOUS DELIVERY
S I M S D E LT E C , I N C .
i
The issue date of this Operators Manual is included on the back cover for
the clinicians information. In the event one year has elapsed between the
issue date and product use, the clinician should contact SIMS Deltec, Inc.
to see if a later revision of this manual is available.
Technical Assistance
If you have comments or questions concerning the operation of the
CADD-Legacy pump, please call the appropriate number given below.
When calling, please specify your pumps software module. This informa-
tion is located on the start-up screen.
CADD, Medication Cassette Reservoir design, CADD-Legacy, and Medication Cassette are
SIMS trademarks. (The symbol indicates it is registered in the U.S. Patent and Trademark
Office and certain other countries.)
The products described are covered by one or more of the following: U. S. Patent Nos.
4,559,038; 4,565,542; 4,650,469; 5,364,242; 5,531,697; 5,538,399; 5,540,561; 5,564,915;
5,567,119; 5,567,136; 5,647,854; 5,695,473; Japanese Patent No. 2034590; European
Patent No. 0182502; other patent(s) pending, foreign patent(s) pending.
ii
Warnings
This Operators Manual should be used by clinicians only. Do
not permit patients to have access to this manual, as the informa-
tion contained would allow the patient complete access to all
programming and operating functions. Improper programming
could result in death or serious injury to the patient.
iii
When the Air Detector is turned off, the pump will not detect air
in the fluid path. Periodically inspect the fluid path and remove
any air to prevent air embolism.
iv
If the pump is dropped or hit, the battery door tabs may break.
Do not use the pump if the battery door or tabs are damaged
because the batteries will not be properly secured; this may result
in loss of power and non-delivery of drug.
Close the fluid path tubing with the clamp before removing the
cassette from the pump to prevent unregulated gravity infusion.
Ensure that the entire fluid path is free of all air bubbles before
connecting to the patient to prevent air embolism.
Cautions
Do not operate the pump at temperatures below +2C (36F) or
above 40C (104F).
Do not store the pump for prolonged periods with the batteries
installed.
vi
vii
ix
Section 5: Reference 39
Messages and Alarms, Alphabetical List .................................... 39
Cleaning the Pump and Accessories ............................................ 43
Exposure to Radiation, Ultrasound, Magnetic Resonance
Imaging (MRI), or Use near ECG Equipment .......................... 45
Technical Description ................................................................. 46
Specifications (Nominal) ....................................................... 47
Accuracy Test Results ........................................................... 51
Safety Features and Fault Detection ...................................... 53
Software Safety Features ....................................................... 55
Data Handling Software Safety Features ............................... 56
Annual Functional Inspection and Testing Procedures .......... 57
Inspection Procedures ........................................................... 57
Testing Procedures ................................................................ 58
Occlusion Pressure Range Tests ............................................ 63
Accuracy Tests ...................................................................... 66
Index .......................................................................................... 71
Limited Warranty ....................................................................... 73
Introduction
The CADD-Legacy 1 ambulatory infusion pump provides mea-
Description
sured drug therapy to patients in hospital or outpatient settings.
General
Therapy should always be overseen by a physician or a certified,
licensed healthcare professional. As appropriate to the situation, the
patient should be instructed in using and troubleshooting the pump.
Indications
The CADD-Legacy 1 pump is indicated for intravenous, intra-
arterial, subcutaneous, intraperitoneal, epidural space, or subarach-
noid space infusion. The pump is intended for therapies that require
a continuous rate of infusion.
Epidural/Subarachnoid Administration
The selected drug must be used in accordance with the indications
included in the package insert accompanying the drug. Administra-
tion of any drug by this pump is limited by any warnings, precau-
tions, or contraindications in the drug labeling.
Analgesics
Administration of analgesics to the epidural space is limited to use
with indwelling catheters specifically indicated for either short-or
long-term drug delivery.
Administration of analgesics to the subarachnoid space is limited to
use with indwelling catheters specifically indicated for short-term
drug delivery.
Anesthetics
Administration of anesthetics to the epidural space is limited to use
with indwelling catheters specifically indicated for short-term drug
delivery.
WARNING:
Symbols
~ Alternating Current (Power Jack)
O Accessory Jack
Description
General
! Attention, consult accompanying documents
(read Instructions for Use)
K Class II Equipment
J Type CF Equipment
D Date of Manufacture
SN Serial Number
Pump Diagram
Display
Description
Power Jack
General
Accessory Jack
Front
AC Indicator
Light
View
Air Detector
Keypad
Cassette
Power Jack
symbol
Threaded
Mounting Accessory
Hole Jack symbol
Battery
Compartment Rear
View
Cassette Lock
Description
General
Display
The Liquid Crystal Display (LCD) shows programming information
and messages. In this manual, the term display is synonymous
with display panel or LCD.
Keypad
The keys on the keypad are described below. A key beeps when
pressed if it is operable in the current lock level.
is used to fill the tubing and to remove air bubbles from the
fluid path.
is used to put the pump into a low power state when not in
use or back into full power.
Power Jack
You may plug an AC Adapter into the Power jack as an alternate
source of power. The indicator light on the front of the pump will
illuminate when the AC Adapter is in use.
Description
General
Accessory Jack
This jack is used for accessory cables. See the Instructions for Use
supplied with those accessories.
Air Detector
The Air Detector is on the pump in the area shown in the diagram.
If air is detected in the part of the tubing that passes through the Air
Detector, an alarm sounds and delivery stops. (See Section 5 for Air
Detector specifications.) If an Air Detector is not desired, it may be
turned off. (See Section 4, Biomed Functions.)
WARNING: When the Air Detector is turned off, the pump will not
detect air in the fluid path. Periodically inspect the fluid path and
remove any air to prevent air embolism. Air embolism could result
in death or serious injury to the patient.
Cassette
The cassette is the portion of the Medication Cassette Reservoir or
CADD Administration Set that attaches to the bottom of the
pump. The following single-use products are compatible with the
CADD-Legacy pump:
Description
General
Threaded Mounting Hole
The optional Polemount Bracket Adapter attaches to the threaded
mounting hole in the back of the pump, allowing you to hang the
pump on an IV pole.
Battery Compartment
Two AA batteries fit into the battery compartment. The AA batter-
ies serve as the primary source of power, or as a backup when an
AC Adapter is in use.
Cassette Lock
This attaches the cassette (the part of the Medication Cassette
Reservoir or CADD Administration Set that attaches to the pump)
to the pump. This allows you to secure the cassette to the pump. If
the cassette becomes unlocked while the pump is running, delivery
will stop and an alarm will occur. If the cassette becomes unlocked
while the pump is stopped, an alarm will occur.
When stopped:
Lock Levels
Lock levels are used to limit patient access to certain programming
and operating functions. The table on the next page lists the func-
tions that are accessible in Lock Level 0 (LL0), Lock Level 1 (LL1),
and Lock Level 2 (LL2). When a function is accessible, the key
Description
General
associated with the function beeps when pressed. If a function is not
accessible, the pump ignores the key press and a beep does not
sound. Section 2, Pump Setup and Programming, describes how to
change the lock level.
Security Codes
The following security codes are preset by the manufacturer for the
clinicians use:
** text omitted from online version **
10
11
1. Push down and hold the arrow button while sliding the
door off.
Pump Setup &
Programming
NOTE:
Be sure to match the polarity markings of the new batteries
(+ and ) with those labeled in the battery compartment. If
you put the batteries in backwards, the display panel will be
blank, and you will not hear a beep.
12
13
14
NOTE:
The life of the batteries is dependent on the amount of
medication delivered, delivery rate, battery age, and the
temperature.
At the rate of one 50 ml Medication Cassette Reservoir per
day, alkaline batteries will usually last about seven days.
15
Watching Power Up
When you install the batteries, the pump will start its power up
sequence during which it performs self-tests and displays pro-
grammed values. Watch for the following:
16
17
18
Delivery Method
The CADD-Legacy 1 pump provides delivery in milliliters per 24
hours:
Continuous Rate (up to 3000 ml per 24 hours)
Delivery Rate
(ml / 24 hrs)
Programming Screens
These are the programming screens for the CADD-Legacy 1
pump. Descriptions of the screens follow.
Given Given
2.50 ml
19
Reservoir Volume
Enter the volume of fluid contained in a filled fluid container. The
Reservoir Volume value decreases as the pump delivers fluid or as
you prime the tubing. When you change the fluid container, reset
the reservoir volume on this screen. If you do not wish to use the
Reservoir Volume feature, scroll down to Not In Use (located
before 1 and after 9999 in the range of values).
The reservoir volume could be set higher than the capacity of the
fluid container. Be sure to program the reservoir volume to reflect
the actual volume of the medication being used.
Pump Setup &
Programming
Continuous Rate
Enter the continuous rate of medication delivery in milliliters per 24
hours. The maximum rate is 3000 ml/24 hrs.
NOTE: If you intend to run the pump in Lock Level 1 so the
Continuous Rate can be varied, you should enter the maximum
allowable rate while programming in Lock Level 0. After program-
ming, you may then change to Lock Level 1 and decrease the rate
to its starting value. See Programming with Upper Limits, Adjusting
Rate in LL1 at the end of Section 2.
Given
This screen shows the total amount of drug delivered since the last
time this value was cleared. The amount shown is rounded to the
nearest 0.05 ml. If this value reaches 99999.95, it automatically
returns to 0 and continues counting. The Given amount does not
include drug used when priming the tubing.
20
Press to begin.
Press .
Press .
Press .
Press .
21
Press .
Press .
Press .
22
Removing a Cassette
WARNING: Close the fluid path tubing with the clamp before
Programming
infusion, which could result in death or serious injury to the patient.
3. Insert a coin into the lock and turn it clockwise. The lock
will pop out when you unlock the cassette.
23
Attaching a Cassette
Obtain a new, filled Medication Cassette Reservoir, or CADD
Administration Set attached to a non-vented, flexible IV bag.
2. Insert the cassette hooks into the hinge pins on the pump.
1999-08-17 D. Zurn
Lgc Attach Cass Coin
24
4. Insert a coin into the lock, push in, and turn counterclock-
wise until the line on the lock lines up with the arrow on the
side of the pump and you feel the lock click into place.
1999-01-23 D. Zurn
Lgc Twist 50 ml
25
NOTE: If you are not changing the fluid container but wish to
prime the fluid path, you may prime the pump as described below.
WARNING: Do not prime the fluid path with the tubing connected
to a patient as this could result in overdelivery of medication or air
embolism, which could result in death or serious injury to the
Pump Setup &
Programming
patient.
2. Press and hold . You will hear a single beep, and the
word Prime will appear on the display.
3. After Prime and three sets of dashes appear, and you hear
three beeps, release .
4. Press and hold again to fill the fluid path and to elimi-
nate air bubbles. The screen displays Priming . . . and you
will hear a short beep each time the pump goes through a
delivery cycle.
NOTE:
The air detector alarm is automatically disabled when
priming.
Fluid delivered during priming is subtracted from the
Reservoir Volume, but is not added to the Given screen
since this fluid is not delivered to the patient.
26
27
2. Place the tubing over the groove in the air detector and tuck
it under the catch.
Catch
28
3. To seat the tubing into the groove, gently pull the tubing
upward, until it is under the retention nubs and flat in the
groove.
29
NOTE: You may change the lock level at any time by stopping the
pump and following the procedure below.
1. Press .
Pump Setup &
Programming
30
Operating
the Pump
press .
31
32
Operating
the Pump
To start the pump
33
34
Functions
Biomed
4. Press to select the setting you wish to view or change,
then follow the instructions in this section for the appropri-
ate screen.
NOTE: To leave a Biomed Function unchanged, press .
35
WARNING: When the Air Detector is turned off, the pump will not
detect air in the fluid path. Periodically inspect the fluid path and
remove any air to prevent air embolism. Air embolism could result
in serious injury or death to the patient.
36
Functions
4. Press to enter the change.
Biomed
37
38
5.0 Reference
39
TWO -TONE ALARM clamp and remove the pump from use.
Contact Customer Service to return the
pump for service.
40
41
42
CAUTION:
Do not immerse the pump in cleaning fluid or water. Do not
allow solution to soak into the pump, accumulate on the keypad,
or enter the battery compartment. Moisture build-up inside the
pump may damage the pump.
Do not clean the pump with acetone, other plastic solvents, or
abrasive cleaners, as damage to the pump may occur.
Routinely clean the pump to keep it free of dirt, liquids, and foreign
objects.
Use any of the following solutions to clean the pump and accesso-
ries:
Soap solution
Benzalkonium Chloride concentrate (0.13%)
Glutaral Concentrate, USP (2%)
10 percent solution of household bleach (one part house-
hold bleach to nine parts water)
Alcohol, USP (93%)
Isopropyl Alcohol, USP (99%)
Chlorohexidine (70%)
PDI Super Sani-Cloth
Mada Medical MadaCide
Reference
2. Wipe the entire surface dry with another soft, lint-free cloth.
Allow the pump to dry completely before use.
43
44
CAUTION:
Do not expose the pump to therapeutic levels of ionizing radia-
tion as permanent damage to the pumps electronic circuitry may
occur. The best procedure to follow is to remove the pump from
the patient during therapeutic radiation sessions. If the pump
must remain in the vicinity during a therapy session, it should be
shielded, and its ability to function properly should be confirmed
following treatment.
Do not expose the pump directly to ultrasound, as permanent
damage to the pumps electronic circuitry may occur.
Do not use the pump in the vicinity of magnetic resonance
imaging (MRI) equipment as magnetic fields may adversely affect
the operation of the pump. Remove the pump from the patient
during MRI procedures and keep it at a safe distance from
magnetic energy.
Do not use the pump near ECG equipment as the pump may
interfere with the operation of the equipment. Monitor ECG
equipment carefully when using this pump.
Reference
45
Technical Description
Standards used in Development of the Pump
46
Specifications (Nominal)
General Pump Specifications
Resolution .......................... Medication Cassette Reservoir or
CADD Administration Set, 0.050 ml per
pump stroke nominal
Size ...................................... 4.1 cm 9.5 cm 11.2 cm [1.6 in. 3.8
in. 4.4 in.] excluding cassette or other
accessories
Reference
47
48
System Operating
Temperature ...................... +2C to 40C (35F to 104F)
System Storage
Temperature ...................... -20C to 60C (-4F to 140F)
System Delivery
Accuracy ............................ 6% (nominal). At low infusion rates,
this accuracy may not be achieved for
short periods. During the total infusion
time, the accuracy averages out (see
accuracy curves, pages 51 and 52)
System Definition .............. System is defined as a CADD-Legacy
pump with an attached Medication
Cassette Reservoir and CADD Exten-
sion Set with integral anti-siphon valve,
or an attached CADD Administration
Set with integral or add-on anti-siphon
valve.
High Pressure Alarm ........ 26 14 psi [1.79 0.97 bar].
Air Detector Alarm ........... Single bubble
Low sensitivity = greater than 0.250 ml
High Sensitivity = greater than 0.100 ml
Multi-bubble = 1.0 ml nominal
Maximum Volume
Infused under Single
Fault Condition ................. CADD Administration Set with
anti-siphon valve: 0.2 ml
Delivery Rate during
Reference
49
Biomed Functions
Air Detector ....................... Off
On-Low
On-High
Default: On-High
Upstream Sensor ............... Off
On
Default: On
Reference
50
36
Flow
24
(ml/hr)
12
0
0 10 20 30 40 50 60 70 80 90 100 110 120
T (min)
% Error
of Flow
T (min)
51
Flow
(ml/hr)
T (min)
% Error
of Flow
T (min)
52
By setting a flag in the memory and not strobing the watchdog, the
microprocessor can force a watchdog time-out. After being reset,
the microprocessor checks the status flag to see if this was a time-
out test. If so, the microprocessor continues normal power-up
Reference
53
than an average of 3 seconds, the circuit will time out and disable
the motor. A unique feature of this circuit is that control lines to
and from the microprocessor circuit allow the microprocessor to
perform a complete functional test of the motor drive circuit with-
out running the motor. The microprocessor performs this test
function every several minutes to assure its continued functionality.
An input from the watchdog circuit prevents motor operation if the
watchdog timer expires. The software verifies this function during
the watchdog test described above.
54
If the stored and calculated CRCs do not match, the software will
display a system fault screen, turn on a continuous two-tone audible
alarm, and stop all drug delivery.
Every time the software receives data from the keyboard encoder, it
55
is checked. If the data is not a valid key press, the software will
disregard the key press. The keyboard is designed with redundant
switches for and . The software must detect that both
switches are activated before taking any action.
not match, the software will display a system fault screen, turn on a
continuous two-tone audible alarm, and stop all drug delivery.
The two calculated values are then compared. If the two values do
not match, the software will display a system fault screen, turn on a
continuous two-tone audible alarm, and stop all drug delivery.
56
Inspection Procedures
Visual Inspection
Reference
57
Mechanical Inspection
Press each key on the keypad. Each key should have a
distinctive dome feeling. The keys should not feel flat.
Attach the battery door. The battery door should fit snugly
in place when it is closed on the pump.
Testing Procedures
Functional Testing
Reference
Power-up Check
Insert batteries or press and observe the LCD during
power up. The first screen will display the serial number,
model number, and software number with revision level.
The second screen will display 32 character blocks. (If
LEC (Last Error Code) and four digits appear prior to the
pump displaying the 32 character blocks, the pump has
experienced an electrical or mechanical fault and should be
58
Lock Check
Attach a 50 or 100 ml Medication Cassette Reservoir or
CADD Administration Set to the pump. The line on the lock
should be aligned with the arrow on the side of the pump.
The following three checks (LCD, Motor and Gear Train and
Reservoir Volume Empty Alarm Check) should be performed in the
sequence shown.
LCD Check
Reference
59
tions).
60
GIVEN Check
61
62
Description
Pressure is generated by activating the pumping mechanism with an
attached filled, clamped Medication Cassette Reservoir. The pump is
started and a fluid is injected until the high pressure alarm sounds.
Equipment needed
50 or 100 ml Medication Cassette Reservoir containing dis-
tilled water
1-ml syringe
Procedure
1. Insert two AA batteries and wait for the pump to power up.
63
Description
An adjustable metered pressure source is connected to the Medica-
tion Cassette Reservoir tubing. The pressure is slowly increased
until the high pressure alarm sounds.
Equipment needed
Procedure
1. Insert two AA batteries and wait for the pump to power up.
1999-01-23 D. Zurn
Lgc Occlusion NoText
64
Reference
65
Accuracy Tests
Gravimetric Accuracy Testing
Description
A Medication Cassette Reservoir is partially filled with water and
weighed, then attached to a pump that is set to deliver a certain
amount of water. The Medication Cassette Reservoir is then
removed and weighed again. The amount of water delivered is
compared to the amount that the pump should have delivered.
Equipment needed
Procedure
1. Fill the 50 or 60 ml syringe with 40 ml of water. Transfer
the water into a Medication Cassette Reservoir.
66
3. Secure the slide clamp as close to the extension set luer lock
connector as possible. This should assure a minimum water
loss from the tubing when the syringe is removed.
6. With the pump in Lock Level 0, set rate to 3000 ml/ 24 hr.
Start the pump and wait for the reservoir volume empty
alarm. The pump will deliver 20 ml.
inaccuracy volume.
67
68
Description
A predetermined amount of water is delivered into a collection
device such as a burette or graduated cylinder. The amount of water
delivered is compared to the amount that the pump is programmed
to deliver.
Equipment needed
50 or 100 ml Medication Cassette Reservoir
50 or 60 ml syringe
CADD Extension Set with Anti-Siphon Valve
A fluid collection device such as a burette or a Class A, 25 ml
capacity graduated cylinder
40 ml of room temperature water
Procedure
Reference
69
70
A C
AC Adapter, 5, 6, 7
cassette, 4, 6
AC indicator light, 4
attaching, 24
accessory jack, 3, 4
cautions, vi
accuracy, 51
removing, 23
accuracy tests
warnings, v
gravimetric, 66
cassette lock, 4, 25
volumetric, 69
cleaning pump, accessories, 4344
Administration Set
cautions, vi
Anti-Siphon Valve, 6
Continuous Rate, 10, 20, 21, 31
attaching, 24
programming, 21
cautions, vi
removing, 23
warnings, iv D
Air Detector, 4, 6, 16, 28, 36, 50
Downstream Occlusion Sensor, 8
inserting tubing into, 28
status screen, 20, 22
testing, 6162 E
warning, iv
alarms, 39, 48 ECG equipment, interference
analgesics, 1 with, vii, 45
anesthetics, 1 epidural administration, 1
caution, vii warning, iv
Reference
B G
batteries, AA, 7, 47, 48 Given screen, 21
cautions, vi clearing, 21
warnings, v
battery compartment, 4, 7
battery contacts, cleaning, 44
71
programming screens, 19 U
ultrasound, 45
R caution, vi
Upstream occlusion sensor, 7, 37
radiation, exposure to, 45
status screen, 21
caution, vi
testing, 62
reservoir, 6, 7, 20, 41, 47
attaching, 24
cautions, vi W
removing, 23
warnings, iv warnings and cautions, iiivii
72
Limited Warranty
SIMS Deltec, Inc. (the Manufacturer) warrants to the Original Purchaser that the infusion
pump (the Pump), not including accessories, shall be free from defects in materials and
workmanship under normal use, if used in accordance with this Operators Manual, for a
period of one year from the actual date of sale to the Original Purchaser. THERE ARE NO
OTHER WARRANTIES.
This warranty does not cover normal wear and tear and maintenance items, and specifically
excludes batteries, administration sets, extension sets or any other accessory items or
equipment used with the Pump.
Subject to the conditions of and upon compliance with this Limited Warranty, the Manufac-
turer will repair or replace at its option without charge (except for a minimal charge for
postage and handling) any Pump (not including accessories) which is defective if a claim is
made during such one-year period.
The following conditions, procedures, and limitations apply to the Manufacturers obligation
under this warranty:
A. Parties Covered by this Warranty: This warranty extends only to the Original Purchaser
of the Pump. This warranty does not extend to subsequent purchasers. The Original
Purchaser may be a patient, medical personnel, a hospital, or institution which purchases the
Pump for treatment of patients. The Original Purchaser should retain the invoice or sales
receipt as proof as to the actual date of purchase.
B. Warranty Performance Procedure: Notice of the claimed defect must be made in writing
or by telephone to the Manufacturer as follows: SIMS Deltec 1265 Grey Fox Road, St. Paul
MN 55112 U.S.A., 1-800-426-2448 or SIMS Graseby Ltd. WD2 4LG UK, +44 (0)1923
246434. Notice to the Manufacturer must include date of purchase, model and serial
number, and a description of the claimed defect in sufficient detail to allow the Manufacturer
to determine and facilitate any repairs which may be necessary. AUTHORIZATION MUST
BE OBTAINED PRIOR TO RETURNING THE PUMP. If authorized, the Pump must be
properly and carefully packaged and returned to the Manufacturer, postage prepaid. Any loss
or damage during shipment is at the risk of the sender.
C. Conditions of Warranty: The warranty is void if the Pump has been 1) repaired by
someone other than the Manufacturer or its authorized agent; 2) altered so that its stability
or reliability is affected; 3) misused; or, 4) damaged by negligence or accident. Misuse
includes, but is not limited to, use not in compliance with the Operators Manual or use with
nonapproved accessories. The Pump is a sealed unit, and the fact that the seal has been
Reference
broken will be considered conclusive evidence that the Pump has been altered or misused.
Removal or damage to the Pumps serial number will invalidate this warranty.
D. Limitations and Exclusions: Repair or replacement of the Pump or any component part
thereof is the EXCLUSIVE remedy offered by the Manufacturer. The following exclusions
and limitations shall apply:
3. The Pump can only be used under the supervision of medical personnel whose skill
and judgment determine the suitability of the Pump for any particular medical treatment.
73
2. The Original Purchaser and any users authorized by the Original Purchaser are
hereby granted a nonexclusive, nontransferable license to use the Licensed Computer
Program only in conjunction with the single Pump supplied by Manufacturer. The
Licensed Computer Program is supplied only in machine-readable object code form and is
based upon Manufacturers proprietary confidential information. No rights are granted
under this license or otherwise to decompile, produce humanly readable copies of, reverse
engineer, modify or create any derivative works based upon the Licensed Computer
Program.
3. All other terms and conditions of this Limited Warranty shall apply to the Licensed
Computer Program.
The Manufacturer disclaims responsibility for the suitability of the Pump for any particular
medical treatment or for any medical complications resulting from the use of the Pump. The
Manufacturer shall not be responsible for any incidental damages or consequential damages
to property, loss of profits, or loss of use caused by any defect or malfunction of the Pump.
This warranty gives the Original Purchaser specific legal rights, and the Original Purchaser
may have other legal rights which may vary from state to state.
Reference
74
European Representative:
SIMS Graseby Ltd.
WD2 4LG UK
+44 (0)1923 246434
2000-03
40-3935-51D 19875