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EVS-EN IEC 61010-2-101:2022/A11:2022

Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Safety requirements for in vitro diagnostic (IVD) medical equipment

General information

Valid from 01.12.2022
Base Documents
EN IEC 61010-2-101:2022/A11:2022
Directives or regulations
None

Standard history

Status
Date
Type
Name
01.12.2022
Main
01.12.2022
Main + amendment
The scope of the Amendment is the same as EN 61010-2-101:2017. It applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes.

Required fields are indicated with *

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