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DS/EN ISO 20417

Medical devices – Information to be supplied by the manufacturer (ISO 20417:2021)

active, Most Current
Organization: DS
Publication Date: 10 May 2021
Status: active
Page Count: 86
ICS Code (Medical equipment in general): 11.040.01
scope:

This document specifies the requirements for information supplied by the manufacturer for a medical device or accessory, as defined in 3.1. This document includes the generally applicable requirements for identification, marking and documentation of a medical device or accessory. This document does not specify the language to be used for such information, nor does it specify the means by which the information is to be supplied. This document has been prepared to support:
- the essential principles of safety and performance for the information supplied by the manufacturer of a medical device according to ISO 16142-1:2016 (see Annex C); and
- the essential principles of safety and performance for the information supplied by the manufacturer of an IVD medical device according to ISO 16142-2:2017 (see Annex C);
- IMDRF/GRRP WG/N47:2018 [3] (see Annex D); and
- IMDRF/GRRP WG/N52:- [4] (see Annex D).

Document History

DS/EN ISO 20417
May 10, 2021
Medical devices – Information to be supplied by the manufacturer (ISO 20417:2021)
This document specifies the requirements for information supplied by the manufacturer for a medical device or accessory, as defined in 3.1. This document includes the generally applicable...
Medical Devices – Information to be provided by the manufacturer (ISO/DIS 20417:2019)
This document specifies the requirements for information supplied by the manufacturer for a medical device or accessory, as defined in 3.1. This document includes the generally applicable...

References

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