Integra A1112, Instruction Manual

Page: 9 / 64

EN – ENGLISH
9 8
Phase Time
(Min.)
Water
Temperature
Detergent and
Concentration
Pre-wash 1 4:00 Cold water N/A
Enzyme
Wash
4:00 Hot water Neutral pH
enzymatic (e.g.
Endozime® AW
Triple Plus with
APA, Ratio 1:128)
Wash 1 10:00 60.0ºC
(140º F)
Neutral pH
detergent
(e.g. Renu-
Klenz™ , Steris,
Ratio 1:256)
Rinse 1 0:30 Hot water N/A
Thermal
Rinse**
2:00 82.2ºC
(180º F)
N/A
** Optional phase for disinfection of components –
minimum water temperature as indicated or per worker
manufacturer specifications for the thermal rinse cycle.
NOTE – Any deviation from this guideline could result in
damage to the equipment as well as improper cleaning
results.
Rinse with purified water. Do not perform if parameters
cannot be achieved.
5. Remove from washer and dry completely if needed.
6. Inspect equipment to make sure there is no visible
organic debris or residue from cleaning agent.
Repeat process if any visible soil is detected.
Lubrication
It is important that metal movable parts be properly
lubricated to keep these parts functional.
Inspection:
Carefully inspect all parts after each cleaning to assure all
components are in proper working con-dition.
CAUTION:
Components should be returned for repair if wear
is noted.
The life expectancy of the MAYFIELD products is expected
to be as long as 7 years.
Maintenance and Care
To ensure proper function and to extend the life and
performance of the equipment, Integra LifeSciences
recommends the following:
Recommended Action Recommended Frequency
Return the device to
the Integra LifeSciences
Repairs department for
detailed inspection and
servicing. Once / year
Request that Integra
NeuroSpecialists perform
routine inspections of the
device Twice / year
In the absence of proper care and servicing of the device,
negative effects may be seen after repeated processing
over time which may lead to reduced performance.
Contact information: See the Service and Repair section
for contact information on how to return your device for
periodic servicing and to request periodic inspections.
See Inspection and/or Service notes section for routine
checks to be performed on the device.
NOTE
– Any serious incident that has occurred in relation
to the device for the user and/or the patient should
be reported to the manufacturer and the competent
authority of the member state in which the user and/or
patient is established.
Device Disposal
NOTE: Follow hospital procedures for disposal of this
device.