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Post-use Maintenance
5-3
Packaging, Sterilizing, Drying and Storage (Motor)
1
Insert the motor into an FDA-approved sterilization pouch that conforms to ISO 11607-1, and seal
the pouch.
2
Perform steam sterilization with the following conditions.
Type Gravity Displacement Pre-Vacuum (Dynamic Air Removal)
Temperature 132°C 132°C
Full Cycle Time 15 min. or longer 4 min. or longer
Drying Time 30 min. or longer 30 min. or longer
3
Store the motor in a clean location without humidity.
CAUTION
ŘUse an FDA-approved steam sterilizer to perform sterilization.
ŘFollow local rules, regulations, and guidelines regarding the reprocessing of devices.
ŘImmediately after sterilization is complete (within 1 hour), remove the motor from the sterilizer. Failure to do so
may cause corrosion.
ŘDo not sterilize the control unit, main unit, AC adapter, AC power cord, motor cord.
ŘDo not lubricate the motor. It may cause overheating and product failure.
ŘDo not perform steam sterilization the product with other instruments even when it is in a pouch. This is to
prevent possible discoloration and damage to the product from chemical residue on other instruments.
ŘDo not heat or cool the product too quickly. Rapid change in temperature could cause damage to the motor.
ŘTo avoid product failure, do not use a sterilizer that exceeds a cycle temperature of 136°C, including the dry
cycle. In some sterilizers, the chamber temperature may exceed 136°C. Contact the sterilizer manufacturer for
detailed information about cycle temperatures.
ŘDo not touch the product immediately after steam sterilization as it will be very hot and must remain in a sterile
condition.
ŘSteam sterilization is recommended for the product. The validity of other sterilization methods (such as plasma
sterilization or EOG sterilization) is not confirmed.
ŘKeep the product in suitable atmospheric pressure, temperature, humidity, ventilation, and sunlight. The air
should be free from dust, salt and sulphur.
ŘSterility is not guaranteed after the sterility retention period specified by the manufacturer and seller of the
sterilization pouch has elapsed. If the sterility retention period has elapsed, perform sterilization again with a new
sterilization pouch.
NOTICE
NSK recommends Class B sterilizers as stated in EN 13060.