logo

Standards Manage Your Business

We Manage Your Standards

IEC

IEC 61010-2-101:2018 (EN-FR)

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

Standard Details

IEC 61010-2-101:2018 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes. It has the status of a group safety publication, as specified in IEC Guide 104. This document has been prepared in close collaboration with Working Group CENELEC BTTF 88.1. This third edition cancels and replaces the second edition published in 2015. This edition constitutes a technical revision. This edition includes the following significant technical changes with respect to the previous edition:
- adaptation of changes introduced by Amendment 1 of IEC 61010-1;
- added tolerance for stability of AC voltage test equipment to Clause 6.
This Part 2-101 is intended to be used in conjunction with IEC 61010-1. It was established on the basis of the third edition (2010) and its Amendment 1 (2016).

General Information

Status : ACTIVE
Standard Type: Main
Document No: IEC 61010-2-101:2018 (EN-FR)
Document Year: 2018
Pages: 34
Edition: 3.0
  • Section Volume:
  • TC 66 Safety of measuring, control and laboratory equipment

Life Cycle

Currently Viewing

ACTIVE
IEC 61010-2-101:2018 (EN-FR)
Knowledge Corner

Expand Your Knowledge and Unlock Your Learning Potential - Your One-Stop Source for Information!

© Copyright 2024 BSB Edge Private Limited.

Enquire now +