DS/EN ISO 20417:2021

Medicinsk udstyr – Krav til generel information, der skal stilles til rådighed af producenten


Status:
Gældende
Type:
Standard
Sprog:
Engelsk
Pris fra:
kr. 847,00
Lovgivning:

Bemærk: Denne standard er endnu ikke harmoniseret, og giver derfor ikke formodningsret. Indtil harmonisering af denne standard er opnået, kan følgende benyttes:


Lovgivning

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Beskrivelse

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).



Antal sider: 86

Udgivet: 2021-05-12

Godkendelsesdato: 2021-05-10

Internationale relationer : EN ISO 20417:2021 IDT ISO 20417:2021 IDT

ICS: 11.040.01 - Medicinsk udstyr. Generelt

Varenummer: M329350


Udvalg og komiteer

Komite

  • ISO/TC 210
  • ISO/TC 210/WG 2