IEC - International Electrotechnical Commission - IEC 61010-2-101:2018 RLV
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
|Organization:||IEC - International Electrotechnical Commission|
|Publication Date:||5 October 2018|
|ICS Code (Diagnostic equipment):||11.040.55|
|ICS Code (Electrical and electronic testing):||19.080|
IEC 61010-2-101:2018 RLV contains both the official IEC International Standard and its Redline version. The Redline version is not an official document, it is available in English only and... View More
IEC 61010-2-101:2018 RLV contains both the official IEC International Standard and its Redline version. The Redline version is not an official document, it is available in English only and provides you with a quick and easy way to compare all the changes between the official IEC Standard and its previous edition.
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).