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- Immediate download
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- Printed Edition
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About This Item
Full Description
Health care personnel have the responsibility to obtain and review manufacturers' data and recommendations and to ensure that they have the necessary resources to follow manufacturers' instructions thoroughly. This TIR can serve as a resource for identifying the questions health care personnel should ask manufacturers when considering a product for purchase or when devising a processing protocol for a product already being used.
Document History
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AAMI TIR 12:2020/(R)2023
viewing
Designing, testing, and labeling medical devices intended for processing by health care facilities: A guide for device manufacturers- Most Recent
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AAMI TIR12:2010
Designing, testing and labeling reusable medical devices for reprocessing in health care facilities: A guide for medical device manufacturers- Historical Version
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AAMI TIR12:2004
Designing, testing and labeling reusable medical devices for reprocessing in health care facilities: A guide for medical device manufacturers- Historical Version
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AAMI TIR 12-94
Designing, Testing, and Labeling Reusable Medical Devices for Reprocessing in Health Care Facilities: A Guide for Manufacturers- Historical Version