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Direct Part Marking (DPM) requirements for Class II Medical Devices

#1
All,
I have received conflicting advice on Direct Part Marking (DPM), for Class II devices.
Our devices are reprocessed and packaged in a kit. The kit has its own UDI information. For the DPM (DI + PI) does it have to be human readable AND AIDC?
Thank you!
 
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