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naSRPS EN ISO 15223-1:2021/prA1:2024

Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements - Amendment 1: Addition of defined term for authorized representative and Modified EC REP symbol to not be country or region specific (ISO 15223 1:2021/DAM 1:2024)

General information

40.60     Jul 25, 2024

ISS

Z076

European Norm

01.080.20     11.040.01  

English  

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

2017/746

Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU

2017/745

Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC

Life cycle

NOW

PROJECT
naSRPS EN ISO 15223-1:2021/prA1:2024
40.60 Close of voting
Jul 25, 2024

Related project

Adopted from EN ISO 15223-1:2021/prA1 IDENTICAL

Adopted from ISO 15223-1:2021/Amd 1:2025 IDENTICAL