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NEMA MITA RMD P1

contributor authorNEMA - National Electrical Manufacturers Association
date accessioned2020-09-15T20:26:20Z
date available2020-09-15T20:26:20Z
date copyright2019
date issued2019
identifier otherZIQXGGAAAAAAAAAA.pdf
identifier otherZIQXGGAAAAAAAAAA.pdf
identifier urihttps://lib.yabesh.ir/std/handle/yse/288638
description abstractIntroduction Medical devices are subject to a number of post-sale aftermarket activities, including servicing, upgrading, updating, refurbishing, and remanufacturing. These activities, when performed correctly and in conformance with applicable Federal regulations, can ensure safe and effective performance over the lifecycle of the device. Unfortunately, these activities are not always performed correctly with applicable oversight, creating potential patient safety and device performance issues
languageEnglish
titleConsiderations for Remanufacturing of Medical Imaging Devicesen
titleNEMA MITA RMD P1num
typestandard
page12
statusActive
treeNEMA - National Electrical Manufacturers Association:;2019
contenttypefulltext


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