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AAMI To Address Reprocessing Concerns In “Technical Reports” Due In 2013

This article was originally published in The Gray Sheet

Executive Summary

Reports are being developed with input from FDA and will cover endoscope reprocessing, standardized cleaning instructions and human factors for device reprocessing.

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Lumened Device Designs Should Facilitate Reprocessing – FDA/AAMI Meeting

Manufacturers of reusable devices with lumens and difficult-to-reach channels should design them so that they can more easily be disassembled for cleaning and subsequently reassembled, according to participants at a recent medical device reprocessing summit.

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