Skip to main content
Back

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
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 *

*
*
*
PDF
16.12 € incl tax
Paper
16.12 € incl tax
Browse standard from 2.48 € incl tax
Standard monitoring

Customers who bought this item also bought

Main

EVS-EN IEC 61326-2-6:2025

Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical electrical equipment
Newest version Valid from 01.09.2025
Amendment

EVS-EN IEC 61326-1:2021/A11:2026

Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 1: General requirements
Valid from 04.05.2026
Amendment

EVS-EN 60825-1:2014/A11:2021

Safety of laser products - Part 1: Equipment classification and requirements
Valid from 01.03.2021