AAMI/ISO 22442-1:2016

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AAMI/ISO 22442-1:2016

2016

Most Recent

Medical devices utilizing animal tissues and their derivatives – Part 1: Application of risk management

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Applies to medical devices other than in-vitro diagnostic medical devices manufactured utilizing materials of animal origin, which are non-viable or have been rendered non-viable. Specifies, in conjunction with ANSI/AAMI/ISO 14971, a procedure to identify the hazards and hazardous situations associated with such devices, to estimate and evaluate the resulting risks, to control these risks, and to monitor the effectiveness of that control. Outlines the decision process for the residual risk acceptability, taking into account the balance of residual risk, as defined in ANSI/AAMI/ISO 14971, and expected medical benefit as compared to available alternatives. This part of ANSI/AAMI/ISO 22442 is intended to provide requirements and guidance on risk management related to the hazards typical of medical devices manufactured utilizing animal tissues or derivatives.

AAMI/ISO 22442-1:2016
STANDARD INFO:
Standard NameAAMI/ISO 22442-1:2016
ScopeMedical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management
PublisherAAMI - Association for the Advancement of Medical Instrumentation/International Org. for Standardization
LanguagesEnglish
State
Publication Year2016
Most recent VersionMOST RECENT
Whether to be replaced
Addendum
FILE INFO:
ANSIANSI Approved
File Size1 file , 480 KB
ISBN(s)9781570206658
NoteThis product is unavailable in Ukraine, Russia, Belarus
Number of Pages35
Published11/17/2016
Same AsAAMI/ISO 22442-1:2016
AAMI/ISO 22442-1:2016
HistoryPublisher Year
AAMI/ISO 22442-1:20162016Current
AAMI/ISO 22442-1:2007/(R)20112008

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