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prSRPS EN IEC 61010-2-101:2025

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

General information

10.99     Jul 14, 2025

ISS

N045

European Norm

11.040.55     19.080  

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

Life cycle

NOW

PROJECT
prSRPS EN IEC 61010-2-101:2025
10.99 New project approved
Jul 14, 2025

Related project

Adopted from prEN IEC 61010-2-101 IDENTICAL

Adopted from IEC 61010-2-101 ED4 IDENTICAL