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IEC 61010-2-101 Ed. 3.0 b:2018

Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
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IEC 61010-2-101 Ed. 3.0 b:2018

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

PUBLISH DATE 2018
PAGES 38
IEC 61010-2-101 Ed. 3.0 b:2018

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

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).

SDO IEC: International Electrotechnical Commission
Document Number IEC 61010
Publication Date Oct. 1, 2018
Language b - English & French
Page Count
Revision Level 3.0
Supercedes
Committee 66
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