Accutron Ultra
Accutron Ultra
Accutron Ultra
• Flushmount
• Flexmount
• Digital Newport
1
INDICATIONS FOR USE
To be used in nitrous oxide-oxygen sedation systems for delivering to a patient
a mixture of nitrous oxide and oxygen gases with a maximum nitrous oxide
concentration of 70%.
CONTRAINDICATIONS
Contraindications for use of nitrous oxide/oxygen inhalation may include:
1. some chronic obstructive pulmonary diseases;
2. severe emotional disturbances or drug-related dependencies;
3. first trimester of pregnancy;
4. treatment with bleomycin sulfate;
5. methylenetetrahydrofolate reductase deficiency.
6. severe asthma
WARNINGS
To be used only by a professional trained in the use of nitrous oxide, using titra-
tion method.
Patient should always be closely monitored during nitrous oxide use. If patient
has an adverse reaction, reduce or stop the flow of nitrous oxide as needed. The
O2 flush button can be used to rapidly purge the lines of N2O. If patient does not
show signs of quick recovery, remove nasal hood and treat with pure oxygen from
either the O2 resuscitator fitting or an auxiliary oxygen tank using a demand valve,
oxygen assisted manual resuscitator, or equivalent. Call for emergency assistance if
rapid response is not achieved.
Do not use this device for the administration of general anesthesia or as part of, or
in conjunction with, a general anesthesia administration system.
For use with 100-240 V AC, 50/60 Hz only.
Use only hospital grade power cord connected to an equivalent receptacle marked
“Hospital Only” or “Hospital Grade.” For emergency power shut-off and isolation,
unplug power cord from wall outlet.
Unit is calibrated at the factory to ±5% per industry recommendations.
Verify that the correct gases are being delivered to the correct flowmeter inlets by
performing the oxygen failsafe test in section VII.
NIOSH recommends N2O levels in operator area be kept below 25 PPM.
Administer pure oxygen to patient for at least 5 minutes after nitrous oxide
procedure.
2
CAUTIONS
Federal (U.S.) law restricts this device to sale by or on order of a dentist or physician.
Do not attempt to repair, alter, or calibrate this device. Unauthorized repair, altera-
tion or misuse of this device is likely to adversely affect the performance and will
void the warranty.
Always use clean, dry medical gases. Introduction of moisture or other contaminants
into Accutron analgesia gas machines may result in defective operation.
Users of electronic flowmeters that control % oxygen should be aware that Accutron
controls % nitrous oxide.
Recycling
Old electrical and electronic equipment must be disposed sepa-
rately and may not be included in the regular domestic waste.
Dispose in accordance with prevailing ordinances. Alternatively,
the unit can be handed over to Accutron for correct recycling.
3
INDICATIONS D’UTILISATION
Vous ne devez utiliser cette machine que dans des systèmes de sédation oxy-
gène-oxyde nitreux qui livrent au patient un mélange de gaz d’oxyde nitreux et
d’oxygène ayant une concentration maximale d’oxyde nitreux de 70 %.
CONTRE-INDICATIONS
Les contre-indications sur l’inhalation d’oxyde azoteux/oxygène peuvent inclure:
1. certaines maladies respiratoires obstructives chroniques;
2. des troubles émotionnels graves ou des dépendances liées à la toxicomanie;
3. le premier trimestre d’une grossesse;
4. le traitement au sulfate bléomycinique;
5. une déficience en réductase d’acide tétrahydrofoliqueméthylène.
6. sever asthme
Dans la mesure du possible, consulter un spécialiste médical avant d’administrer
des agents analgésiques/anxiolytiques aux patients qui présentent des troubles
médicaux sous-jacents (par ex.: maladies respiratoires obstructives graves, défail-
lance cardiaque, drépanocytose, otite moyenne aiguë, greffon récent de la mem-
brane du tympan, traumatisme crânien grave aigu.1 L’opérateur doit examiner
l’historique du patient à l’égard de ces problèmes de santé.
1
American Academy of Pediatric Dentistry. Lignes directrices cliniques: Lignes directrices sur
l’utilisation de l’oxyde azoteux pour les patients dentaires pédiatriques. Pediatr Dent 2009;31(6): 148-
151. Disponible sur le site Web: “http://www.aapd.org/media/policies.asp”. Accès le 23 février 2010.
AVERTISSEMENTS
Pour être utilisé uniquement par un professionnel formé à l’utilisation de l’oxyde
nitreux en utilisant la méthode de titration.
Le patient doit toujours faire l’objet d’une surveillance étroite pendant l’utilisation
de l’acide azoteux. Si le patient présente des effets indésirables, réduire ou arrêter
le débit de l’acide azoteux, selon le besoin. Le bouton de purge O2 pour peut être
utilisé pour évacuer rapidement les lignes de N2O. Si le patient n’affiche aucun
signe de récupération rapide, enlever l’enceinte nasale de hood et le traiter avec
de l’oxygène pur, soit à partir du raccord du réanimateur O2 ou d’une bouteille
d’oxygène auxiliaire utilisant un détendeur, d’un réanimateur manuel assisté par
de l’oxygène ou l’équivalent. Demander de l’aide d’urgence si une réponse rapide
n’est pas obtenue.
Ne pas utiliser ce dispositif pour l’administration d’une anesthésie générale
ou comme partie ou encore en conjonction avec un système d’administration
d’anesthésie générale.
Pour une utilisation à 100-240 V AC, 50/60 Hz seulement.
Utilisez le cordon d’alimentation de qualité que l’hôpital connecté à une prise
équivalente portant la mention «Hôpital seulement» ou «Hospital Grade». Pour
pouvoir d’arrêt d’urgence et d’isolement, débranchez le cordon d’alimentation
de la prise murale.
Unité est calibré à l’usine de ± 5% selon les recommandations de l’industrie.
Vérifiez que le bon gaz sont livrés au bon débitmètre anses en effectuant l’oxygène
Failsafe Test dans la section VII.
Le NIOSH (USA) recommande N2O niveaux de zone opérateur être maintenu en
dessous de 25 ppm.
Administrer oxygène pur pour au moins 5 minutes après utilisation d’azote.
4
ATTENTION
Conformément à la loi fédérale des États-Unis, cette machine ne peut être vendue
que par un dentiste ou par un médecin ou sur leur ordonnance.
Utilisez toujours des gaz médicaux propres, secs. Toute introduction d’humidité
ou d’autre contaminant dans un appareil d’analgésie à gaz Accutron provoquera
un mauvais fonctionnement.
Recyclage
Les anciens équipements électriques et électroniques doivent
être éliminés séparément et ne peuvent pas être inclus dans
les déchets domestiques réguliers. Éliminer conformément aux
règlements en vigueur. Autrement, l’appareil peut être remis à
Accutron pour le recyclage correct.
5
Table of Contents Page
I. Technical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Flushmount . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Flexmount . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Digital Newport . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
V. General Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
IX. Warranty . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
XII. Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
6
I. TECHNICAL SPECIFICATIONS
Physical
Flushmount Main Unit 8x4x7.5” (20,3x10,2x19 cm) Weight: 5.2 lbs (2,4 kg)
Flushmount Controller 9x4x1.5” (22,9x10,2x3,8 cm) Weight: 1.0 lbs (0,8 kg)
Flexmount 8x4x7.5” (20,3x10,2x19 cm) Weight: 8.2 lbs (3,7 kg)
Digital Newport 19x32x22” (48x80x56 cm) Weight: 75 lbs (34 kg)
Electrical
100-240 V AC 50/60 Hz. 0.5 A
Socket is IEC/EN 60320-1 C14 and accepts an IEC/EN 60320-1 C13 connector
Power cords available for most countries
Internal Battery
Lithium coin battery, 3v CR2032
Fuses
T500mAL, 250v (quantity 2) Accutron part number 26456-FRU
Gas Supply
Oxygen: 50-55 PSI at 100 LPM min.
Nitrous Oxide: 50-55 PSI at 10 LPM min.
Gas Fittings
Oxygen Inlet: Male DISS CGA 1240
Nitrous Oxide Inlet: Male DISS CGA 1040
Mixed Gas Outlet: Male DISS CGA 1160 or 1/4” Hose Barb
Oxygen Resuscitator Connection: 1/4” I.D. Quick Disconnect
Adapter hoses available for AGA, DIN, NIST, BOC, AFNOR, SIS, UNIFO
Gas Delivery
Oxygen Flush: Minimum 20 LPM
Oxygen Flow: 1.0 LPM-9.9 LPM (Accuracy +/- 0.5 LPM)
Oxygen %: 30%-100%
Oxygen Resuscitator Flow: Minimum 100 LPM, 100% O2
Nitrous Oxide Flow: 0-6.9 LPM (accuracy +/- 0.5 LPM)
Nitrous Oxide %: 0-70%
Mixed Gas Flow: 1.0-9.9 LPM
Environmental
Transportation/Storage: Temperature: -40°C to +70°C (-40°F to 158°F)
Humidity: 10-100%
Operating Conditions: Temperature: 15°C to 32°C (68°F to 90°F)
Humidity: 30-75%
Atmospheric Pressure: 72-101 kPa (543-760 mmHg)
Accessories
Printer
Remote Control
Remote Flow System (RFS)
Accu-Vac
Applied Part (rated BF)
Scavenging Circuit II PN32007
Scavenging Circuit II (RFS) PN32009
Scavenging Circuit II, ClearView PN43003
Scavenging Circuit II, ClearView (RFS) PN43004
7
II. CONTROL/DISPLAY FEATURES
Increase
Total
Flow
Increase
% N2O
Decrease
Total
Decrease Flow
% N2O
Power
Cancel/Test Print N2O O2 O2 (On/Off)
Vacuum LED Display Display Flush
Remote Control
Increase
Increase Total Flow
% N2O
Decrease
Total Flow
Decrease
% N2O Power
(On/Off)
O2 Flush
8
Front Control/Display Panel & Remote Control
Control/Display Panel – Easy-to-use control panel allows setting Total Flow and
N2O concentration with the touch of a finger. Bright, color-coded displays make it
simple to monitor status, even from a distance. Optional hand-held Remote allows
functional control at patient chairside.
Total Flow Control – Allows setting of Total Flow in either (.1) LPM or (.5) LPM
increments. Once set, the Total Flow will remain constant even if % N2O is
changed.
Total Flow Display – Shows Total Flow in numeric LPM format with yellow LEDs.
Flush Control – Ceases N2O Flow and provides a minimum of 20 LPM of pure O2
as long as button is pressed.
O2 Flow – Two green LED displays show O 2 Flow in both LPM numbers and
graphic bars simulating standard flow tube.
N2 O Flow – Two blue LED displays show N2O Flow in both LPM numbers and
graphic bars simulating standard flow tube.
Cancel/Test – During an alarm mode, turns off audio alarm for one minute.
During normal mode, performs self-check of all displays.
9
III. FLOWMETER MODELS
FLUSHMOUNT MODEL
Two piece design for easy installation into a cabinet or a wall. Thin control module
located away from main module, power, and gas lines, requires remote outlet.
b) Remote Flow
System (RFS)
(Contains mixed
gas outlet, O2
resuscitator, and
vacuum controller
with gauge display)
Green Light
MIN
MAX
MAX
VAC
O
2
c) Accu-Vac
(Contains mixed gas outlet,
O2 resuscitator, and vacuum
controller with LED display)
10
Remote Control Remote Vacuum 12 V DC Out RS232 Printer
N2O Inlet
DISS
O2 Inlet
DISS
O2 Out – Connects to O2
100-240 V AC Inlet Mixed Gas Out (O2/N2O) Resuscitator fitting on
IEC/EN 60320-1 C14 – Connects to remote remote outlet
with two fuses. bag tee outlet
(Accepts IEC/EN
60320-1 C13 connector)
N2 O Inlet – Labeled N2O IN – Equipped with male CGA 1040 DISS fitting to
prevent gas mix-up.
O2 Out – Labeled O2 OUT – Equipped with male CGA 1240 DISS fitting, provides
oxygen for resuscitator.
Mixed Gas Port – Equipped with male CGA 1160 DISS fitting (Medical Air)
Power Cord Inlet – Clearly labeled 100-240 V AC, 50/60 Hz and protected by two
fuses for added safety. Fuses are 240 V, 0.5A, slow-blow. To disconnect power,
unplug cord. Do not position where this disconnection would be difficult.
RS232 Printer Connector – Clearly labeled and designed for use with optional
Accutron-approved printer.
11
FLEXMOUNT MODEL
Can be mounted on
a number of different
devices.
O2 Resuscitator Fitting
12
Wall Arm and Mobile Stand version
Remote Control Remote Vacuum 12 V DC output RS232 Printer
N2O Inlet
DISS
Note: Australian
version has SIS
fittings and
slightly different
layout.
O2 Inlet
DISS
4 Cylinder version
Remote Control Remote Vacuum 12 V DC output RS232 Printer
N2O Inlet
DISS
O2 Inlet
DISS
O2 OUT – Connects to
100-240 V AC Inlet O2 Resuscitator fitting
IEC/EN 60320-1 C14 on front of unit
With 2 Fuses Mixed Gas Out (O2/N2O) –
(Accepts IEC/EN Connects to bag tee port on
60320-1 C13 connector) front of unit
13
Flexmount Utility Connections
O2 Inlet – Labeled O2 IN – Equipped with male CGA 1240 DISS fitting to prevent
gas mix-up.
N2 O Inlet – Labeled N2O IN – Equipped with male CGA 1040 DISS fitting to
prevent gas mix-up.
Power Cord Inlet – Clearly labeled 100-240 V AC, 50/60 Hz and protected by two
fuses for added safety. Fuse ratings are 240 V, 0.5 A, slow-blow. To disconnect
power, unplug cord. Do not position meter where this disconnection would be
difficult.
RS232 Printer Connector – Clearly labeled and designed for use with optional
Accutron-approved printer.
DIGITAL NEWPORT
Handle Regulators
Warning: Do not and E Yokes
hold handle Line
when Pressure
opening Gauges
cabinet.
Remote
10’ Control Port
Hospital (Optional)
Grade
Power O2
Cord Resuscitator Tank
Fitting Restraint
Gas
Power Socket Cylinders
Removable
Note: Power Cord must be either Bag Tee
unplugged from socket or unwound from If printer option is
storage cleats when opening Newport. installed, printer cable
will extend from cover
To disconnect power, unplug cord. Do not
at this point.
position where this would be difficult.
14
Digital Newport Setup and Connections
View – When looking at the front of the Newport cabinet, Nitrous Oxide is on the
left as shown by the blue Nitrous Oxide gauge. Oxygen is on the right as shown by
the oxygen gauge.
Opening Newport Cabinet – Open the Newport cabinet by placing one hand on
the front cover and the other in the handle on the side. Pull handle back all the
way. Make sure the power cord is unplugged from the socket in the skirt first.
NOTE: Regulators are pinned to match gas cylinders. Connect gas hoses to
regulator outputs.
NOTE: Hoses and regulators use DISS fittings to prevent mix up. Rotate cylinders
so that regulators fit inside.
Open Gas Cylinders – Pick one tank of each gas to be “in use“ tank and attach “in
use” label to cylinder. Open these cylinders using the cylinder wrench provided in
accessory box. Close Newport cabinet.
Connect Power –
1. Plug cord back into skirt outlet
2. Plug other end of cord into receptacle
NOTE: System will operate from 100-240 V, 50-60 Hz. Internal power supply will
switch automatically.
Scavenging Circuit –
- Install bag tee from accessories box into front of Newport.
- Attach scavenging circuit to bag tee.
- Connect vacuum hose to system vacuum.
- Install nasal hood into scavenging circuit and start vacuum flow per
scavenging instructions.
15
Digital Newport: Managing Gas Supply
Note: Power Cord must be either unplugged from socket or unwound from
storage cleats when opening Newport.
1. Identify the two in-use tanks (N2O and O2) by attaching “in-use” identification
tags to them.
2. When one of the in-use tanks is empty, close the tank by turning the valve
clockwise. Leave the empty tank in place.
3. Move the “in-use” tag to the appropriate reserve tank, which now becomes
the in-use tank. Replace the empty tank with a new tank, which then becomes
the reserve tank.
4. Open the valve of the new in-use tank by turning counterclockwise.
Note: Do not open the reserve tank until the in-use tank is empty. When
changing gas tanks, make certain both same gas cylinders that are
involved in the exchange are closed. Always remember to switch
the “in- use” tags over to the new tanks.
5. Contact gas supplier to request new gas cylinders as needed.
16
Digital Newport:
Control Module and Main Module Locations
Control
Module
is behind
shield at
front of
unit.
Serial #
Label
17
IV. SAFETY FEATURES
O2 Fail Safe System – Offers assurance that N2O ceases if the O2 supply is
interrupted or reduced. Alarm will sound, FAILURE OXYGEN LEDs will light,
and N2O flow will cease.
N2 O Supply Warning – Triggers an alarm if the N2O supply cannot keep up with
user’s needs. Alarm will sound and FAILURE NITROUS LEDS will light. Flow
switchs to 100% oxygen.
Mixed Gas Flow to Patient – Monitors pressure in mixed gas line and triggers an
alarm if flow to patient is obstructed. Alarm will sound and FAILURE NITROUS
OXYGEN LEDS will light.
Emergency Air Valve – Automatically provides patient with ambient air if gas flow
is interrupted. Located on remote bag tee.
V. GENERAL INSTRUCTIONS
1. Warranty
Unpack Digital Ultra and inspect to make certain that the unit has not been
damaged during shipment.
The unit’s serial number is located on the back of Digital Ultra (see page 17 for
Digital Newport’s serial number location). Record the serial number in the area
provided at the back of this booklet. Once Digital Ultra Flushmount is mounted
into a cabinet, the serial number will no longer be visible. Always reference the
serial number when corresponding with Accutron.
Complete the warranty card supplied with Digital Ultra and mail to Accutron.
Completion of this step ensures proper device warranty coverage. Accutron Digital
Ultra analgesia machines carry a two-year limited warranty (see Warranty on page
26 for details).
After device installation, connect the oxygen and nitrous oxide supply lines to the
Diameter Specific Instant fittings or DISS fittings located on the back of the device.
See pages 14-16 for information specific to the Digital Newport. It is important that
the regulators for both gases be set to give pressures in the range of 50-55 PSI.
Verify that the correct gases are being delivered to the correct ports on device
before initial use. This can be done by shutting off the O2 cylinders and turning the
unit on. The unit should immediately go into an oxygen failure fault mode. If unit
indicates O2 gas is flowing, lines are crossed. Correct before using.
18
3. Power Connection
Device is designed to run on 100-240 V AC and 50/60 Hz. There is no need to flip
an external switch; the unit automatically adjusts for any power. A medical-grade
power cord is supplied with the unit and must be used to ensure proper ground-
ing. It is important that the power cord be plugged into an outlet marked “Hospital
Only” or “Hospital Grade.” The power cord is plugged into the AC entry, which
contains two fuses and is located on the back of the device. International power
cords are offered for most countries. Use only 240 V, 0.5A, slow-blow fuses. Fuses
can be ordered from Accutron as part number 26456-FRU.
4. Auxiliary Connections
Plug remote control into remote port on back of Digital Ultra or on front cover of
Newport if ordered as option.
Plug Accu-Vac signal line into vacuum connector on back of Digital Ultra
(Flushmount only). Vacuum LED should light when Digital Ultra is powered
indicating vacuum is flowing.
Plug printer cable from Able printer, if used, into RS232 printer port. Do not use this
port for any other devices. If printer is ordered on Newport as option, printer cable
will extend from front cover. Note: Use only Able printer supplied by Accutron.
20
5. % N2O box now displays months. Set the month with Total Flow Up/Down
buttons. Push % N2O Up (+) button to store value and proceed to next step.
6. Total Flow box now displays days. Set the day with Total Flow Up/Down
buttons. Push % N2O Up (+) button to store value and proceed to next step.
7. N2O box now displays the hours. Set the hour with Total Flow Up/Down
buttons. Push % N2O Up (+) button to store value and proceed to next step.
8. N2O box now displays minutes. Set the minute with Total Flow Up/Down
buttons. Push the cancel button to save value and exit program.
Changing Starting Total Flow Rate
With power connected and flowmeter off, press and hold CANCEL/TEST and
Total Flow + (up) Arrow together until beep (5-7 seconds). Current Total Flow
will be shown. Adjust to desired flow rate using Total Flow + Up and Total Flow -
Down buttons. Acceptable values are 1.0 to 9.9 LPM. Press Flush button to accept
new value. Starting Total Flow will now start at the new value.
Application Specifications
Intended Use
The Accutron Digital Flowmeter is used to reduce anxiety in dental patients so that
traditional treatments can be performed more efficiently and with less stress on the
patient.
21
Intended part of the body
Nitrous oxide is a gas and is delivered to the nose via a nasal hood connected to
gas supply tubing. The patient inhales the gas which is then absorbed in the lungs.
Intended user profile
Medical professionals such as doctors, dentists, dental assistants, dental hygienists,
and nurses who have been formally trained in the use of nitrous oxide and who
have studied the operating instructions in the User Manual.
Precise flow of both oxygen and nitrous oxide are achieved through a feedback
circuit containing a proportioning solenoid, a medical grade mass flow sensor, and
the main microprocessor. The mass flow sensors measure flow electronically giv-
ing real time updates to the circuit board which directs the solenoids to maintain
desired flow rates. The processor monitors these flows and gives alarms as needed
if the flow of either gas can not match the desired rates. The software also pre-
vents nitrous oxide from flowing without oxygen and maintains oxygen levels at
30% or more at all times.
Clinical operation is very simple as there are only two items to control, TOTAL
FLOW and %N2O. Press POWER to start flow which comes on at 5.0 LPM Total
Flow and 0 %N2O. Adjust Total Flow with the + and – keys until it matches the
patients breathing rate. Increase % N2O by using the + and – keys until proper
relaxation is achieved. Decrease % N2O to 0 at end of procedure and continue
with pure oxygen for 5 minutes. Turn Power off. Total Flow and %N2O can be
adjusted during procedure as needed. Pure oxygen flush is available at any time.
Print option is also available.
22
Abnormal Use
Training
The intended use is the basis for training which is considered mandatory for all
operators prior to use. General Theory on nitrous oxide use and procedures are
described in such books as Nitrous Oxide and Oxygen Sedation by Clark and
Brunick and Lachgas by Dr Mathers. It is recommended that users undergo class-
room training as well as hands on lab instruction. US training can be found in
numerous ADA sponsored continuing education courses. European training can
be obtained through the Institute for Dental Sedation, Cologne, Germany (http://
www.sedierung.com) or through BIEWER medical (http://www.biewer-medical.
com/en/sedation-training), Koblenz, Germany. Consideration of currently valid
local and national guidelines for training is required.
Turn Digital Ultra on and press CANCEL/TEST button. All displays should light
sequentially with an audio beep, including alarms.
Wipe with damp cloth. Do not allow liquids to touch rear auxiliary connections or
enter case. Do not spray directly onto unit.
23
Outspout Check Valve Test Check Monthly
• Digital Ultra should be off.
• Reservoir bag should be connected to the bag tee downspout.
• Mixed Gas tube should be connected to the outspout but not connected
to the white patient delivery tubing.
• Breathe into the open end of the corrugated tube.
The reservoir bag should not fill.
Factory Check
Recommended every 2 years or more frequently as required by prevailing
local and national codes.
Send equipment to authorized Service Center for operational check, battery
replacement, and recalibration. Note: battery used for time and date info
only, loss of battery does not affect safety or operation.
Routine Maintenance
There is no required routine maintenance as long as recommended factory
check is at least in the recommended period or more frequently as required by
prevailing local and national codes. Unit should only be repaired by trained indi-
viduals with specialized equipment. Unauthorized opening of equipment will put
individual at risk of electrical shock and will void Warranty.
Disinfecting
The following products are approved for disinfecting the front touch pad
area. Do not allow liquid to enter any connectors on back of unit. Do not spray
directly onto unit.
24
VIII. TROUBLESHOOTING GUIDE
PROBLEM POSSIBLE CAUSE REMEDY
Display off 1. Power cord loose 1. Connect cord firmly
2. No power to wall outlet 2. Check circuit breaker
3. Fuse blown and/or call electrician
3. Replace fuse in holder
under AC socket.
Oxygen Failure Low O2 pressure 1. Verify O2 input to
alarm flowmeter
2. Verify valves are open
Nitrous Failure Low N2O pressure 1. Verify pressure in N2O
alarm cylinder
2. Verify valves are open
Nitrous & Oxygen Obstructed flow to patient Remove kinks or
Failure alarm obstructions from mixed
gas line to patient
Front panel buttons 1. Defective panel Contact Accutron
are not operating 2. Internal problem Customer Service
Remote Control is 1. Loose connection to unit 1. Check remote plug
not operating 2. Defective Remote connection on back
3. Internal problem 2. If problem persists
contact Accutron
Customer Service
Displays don’t Broken display/circuit Contact Accutron
work board Customer Service
Automatic Vacuum 1. Loose connection in 1. Check plug connection
port (Accu-Vac) back 2. Verify output of vacuum
doesn’t work 2. Defective valve outlet is 12 +/- 3 V DC
3. Internal problem 3. Verify system vacuum is
4. Insufficient vacuum > 8 in Hg
4. If not solved, contact
Accutron Customer Service
Flush does not have Filter clogged Contact Accutron
enough oxygen O2 solenoid damaged Customer Service
flow
Flush does not work 1. Internal Problem Contact Accutron
at all Customer Service
Flow doesn’t 1. Calibration error Check output with Oxygen
appear to be 2. Internal problem Analyzer if available
accurate Contact Accutron
Customer Service
Unit freezes, 1. Processor problem Unplug power cord
doesn’t respond, Plug back in (Reboot)
gas won’t shut-off
25
IX. WARRANTY
ACCUTRON 2-YEAR FLOWMETER LIMITED WARRANTY
WARRANTY TERMS
Limited Warranty and Disclaimer: Accutron (“Seller”) warrants that its product
will be free from manufacturing defects subject to the terms, conditions, and
limitation set forth hereinafter, for a period of 2 years for flowmeters and 1 year
for other equipment products. Seller’s obligations under this limited warranty
are contingent on Buyer’s full payment of the product purchase price. Except as
specifically set forth above, Seller and its affiliates make no warranties, expressed
or implied, and specifically disclaim any warranties of merchantability or fitness
for a particular purpose.
The liability of Seller and its affiliates for any claims, losses, damages, or expenses
from any cause whatsoever (including acts or omissions of third parties) regardless
of the form of the action, whether in tort, contract, or otherwise, shall not exceed the
repair cost, replacement cost, or purchase price of the product that directly gives
rise to the claim. Seller and its affiliates shall not be liable for any incidental, special,
reliance, consequential, or indirect loss or damage rising out of this agreement or
the products. As used in this paragraph, consequential damages include, but are
not limited to, lost profits, lost revenues, property damage, personal injury damage
to the Purchaser or third parties, loss of business or profits, and/or loss of business
reputation. It is the sole responsibility of Purchaser to determine the suitability of
the products for the Purchaser’s intended use. Seller’s obligation to repair, replace
or refund, as set forth above shall be Buyer’s exclusive remedy.
This warranty constitutes the entire warranty. This warranty and Seller’s liability
hereunder shall be construed according to the laws of the State of Arizona without
regard to conflict of lay principles.
To activate the Flowmeter Warranty, complete and mail the warranty registration
card that accompanies Flowmeter.
Accutron warranties are subject to the following conditions: Accutron products
and equipment are warranted to be free from defects in material and workmanship
under normal use and service, including all component parts. This warranty shall
not apply to defects resulting from accidents, alterations, or misuse. If modifications
have affected the operation of the product to render it faulty, this warranty shall
be void. This warranty shall be void if any part not of Accutron’s manufacture or
supply has been incorporated into the product.
THIS WARRANTY IS GIVEN IN PLACE OF ALL OTHER WARRANTIES
EXPRESSED OR IMPLIED, OF MERCHANTABILITY, FITNESS FOR A
PARTICULAR PURPOSE OR OTHERWISE.
No statement or claim about the product by any employee, agent, representative or
dealer of Accutron, Inc. shall constitute a warranty by Accutron, Inc. or give rise to
any liability or obligation of Accutron, Inc.
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X. WARRANTY AND RETURNED GOODS POLICY
All warranty resolution issues and merchandize returns will be handled through the
local authorized Accutron distributor. Contact distributor where unit was purchased.
XII. ASSISTANCE
For Assistance, contact your local dental distributor or call Accutron Customer
Service at:
Accutron, Inc.
1733 W. Parkside Lane
Phoenix, AZ
USA 85027
www.accutron-inc.com
MT Promedt Consulting GmbH
EC REP Altenhofstrasse 80
D-66386 St. Ingbert/Germany
Tel. +49 (0) 6894-581020
Fax +49 (0) 6894 581021
City/State/Zip: ___________________________________________________
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1733 W. Parkside Lane • Phoenix, Arizona 85027
Toll-free: 800-531-2221 • Local Phone: 623-780-2020 • Fax: 623-780-0444
www.accutron-inc.com
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