Integra MAYFIELD A1051, Instruction Manual

Page: 9 / 64

9
EN – ENGLISH
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.
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.