AAMI TIR30:2011/(R)2016

Click here to purchase
This report is intended as a resource for manufacturers of medical devices who must validate the instructions for reprocessing that they include with their devices. In addition to describing available processes, materials, test methods, and acceptance criteria for cleaning medical devices that are labeled by the manufacturer for reuse and reprocessing, the report also discusses some of the underlying problems and challenges associated with validating a cleaning method. Extensive references and a sample cleaning validation outline and also are included.

Product Details

Published:

08/10/2011

Number of Pages:

60

File Size:

1 file , 460 KB

Part of:

AAMI STBK12-1/STBK12-1-CD