Integra Padgett B, User Manual

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be assumed to be non-sterile and must not be used.
Do not modify this electromechanical equipment in any manner. The dermatome system
contains no user-serviceable components. Unauthorized modifications, including the
use of replacement components or product servicing not provided by an authorized
Integra Padgett Dermatome Repair Center (IPDRC), can result in serious injury to patient
and/or operator.
Precautions
A thorough, manual cleaning process as detailed in the Cleaning and Decontamination
section is recommended for the Electric Dermatome Models B and PI. The Dermatome motor
housing cannot be immersed in liquid cleaners, which would occur in an automated process.
Automated cleaning methods may not be effective and may result in damage and reduced
performance of the device.
EMC Caution: Care should be taken if the equipment is used adjacent to or stacked with other
equipment. If adjacent or stacked use is inevitable, the equipment should be observed to
verify normal operation in the configuration in which it will be used. (Refer to EMC Declaration
Table in the appendix for more detailed electromagnetic emission and immunity information.)
To improve performance and overall safety of the dermatome it is recommended that the
dermatome’s power supply input be connected to a Ground Fault Circuit Interrupter (GFCI)
receptacle.
Prior to use visually inspect the dermatome handpiece and its cable for signs of physical
damage or wear. Do not use the dermatome if damage is observed. Dermatome handpiece
cable damage may include cracks or discoloration of the cable jacket, exposed conductors,
or distortion of the cable or connector. The dermatome handpiece and its attached cable can
only be serviced by the Integra Padgett Dermatome Repair Center (refer to Maintenance and
Servicing Section).
Do not autoclave the power supply or the power supply wall cord.
Never immerse instrument, even to cool. This will result in the unit being damaged and
needing repair.
Used blades should always be disposed of in proper safety containers.
Unit disposal (if necessary) is to be in compliance with your facilities disposal protocols.
Avoid rough handling or dropping the dermatome handpiece and power supply. If rough
handling is suspected or the unit is dropped, it is recommended to assess the condition of the
dermatome system prior to use as outlined in the Troubleshooting section.