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EVS-EN 60601-1:2006/A13:2024

Medical electrical equipment - Part 1: General requirements for safety

General information

Valid from 02.05.2024
Base Documents
EN 60601-1:2006/A13:2024
Directives or regulations
2017/745 Medical devices (MDR)

Standard history

Status
Date
Type
Name
15.05.2024
Main + amendment
02.05.2024
Amendment
01.11.2021
Main + amendment
02.03.2016
Main + amendment
08.12.2006
Main + corrigendum
Amendment to EN 60601-1:2006

Required fields are indicated with *

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Amendment

EVS-EN 60601-1:2006/A2:2021

Medical electrical equipment - Part 1: General requirements for basic safety and essential performance (IEC 60601-1:2005/A2:2020)
Valid from 01.11.2021
Main + amendment

EVS-EN 60601-1-2:2015+A1:2021

Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic disturbances - Requirements and tests (IEC 60601-1-2:2014 + IEC 60601-1-2:2014/A1:2020)
Newest version Valid from 01.04.2021
Main

EVS-EN ISO 10993-1:2026

Biological evaluation of medical devices - Part 1: Requirements and general principles for the evaluation of biological safety within a risk management process (ISO 10993-1:2025)
Newest version Valid from 15.01.2026
Main + amendment

EVS-EN ISO 15223-1:2021+A1:2025

Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021 + ISO 15223 1:2021/Amd 1:2025)
Newest version Valid from 01.12.2025