SR EN IEC 61010-2-101:2023/A11:2023

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

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.

Add to cart

General information

Status : Valid
Approval date : 1/31/2023
Number of pages : 18
ICS : 11.040.55 Diagnostic equipment,19.080 Electrical and electronic testing
Technical Committee : 24 - Measure electronic equipment

Relations with other standards:

Amends SR EN IEC 61010-2-101:2023