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IEC/TR 61010-3

Safety Requirements for Electrical Equipment for Measurement, Control, and Laboratory Use - Part 3: Protocol for the Preparation of Conformity Verification Reports for the IEC 61010 Series

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Organization: IEC
Publication Date: 1 April 2003
Status: inactive
Page Count: 20
ICS Code (Electrical and electronic testing): 19.080
ICS Code (Chemical laboratories. Laboratory equipment): 71.040.10

Document History

IEC/TR 61010-3
April 1, 2003
Safety Requirements for Electrical Equipment for Measurement, Control, and Laboratory Use - Part 3: Protocol for the Preparation of Conformity Verification Reports for the IEC 61010 Series
A description is not available for this item.
TR 61010-3
July 1, 1997
Safety Requirements for Electrical Equipment for Measurement, Control, and Laboratory Use - Part 3: Protocol for the Preparation of Conformity Verification Reports for the IEC 61010 Series
A description is not available for this item.

References

This document is referenced by:
AAMI ES60601-1 - Medical electrical equipment-Part 1: General requirements for basic safety and essential performance
Published by AAMI on January 1, 2005
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
This document is referenced by:
EN IEC 61010-031 - Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 031: Safety requirements for hand-held and hand-manipulated probe assemblies for electrical test and measurement
Published by CENELEC on May 1, 2023
This part of IEC 61010 specifies safety requirements for hand-held and hand-manipulated probe assemblies for electrical test and measurement, and their related accessories. These probe assemblies are...
This document is referenced by:
AAMI TIR62354 - General testing procedures for medical electrical equipment
Published by AAMI on January 1, 2009
Scope and object This technical report applies to MEDICAL ELECTRICAL EQUIPMENT (as defined in Subclauses 3.63 of IEC 60601-1:2005 and 2.2.15 of IEC 60601-1:1988), hereinafter referred to as ME...
This document is referenced by:
CSA Z15190 - Medical laboratories — Requirements for safety
Published by CSA on January 1, 2005
This International Standard specifies requirements for safe practices in the medical laboratory.
This document is referenced by:
ISO 16142-2 - Medical devices - Recognized essential principles of safety and performance of medical devices - Part 2: General essential principles and additional specific essential principles for all IVD medical devices and guidance on the selection of standards
Published by ISO on August 1, 2017
This document, which includes the essential principles of safety and performance, identifies significant standards and guides that can be used in the assessment of conformity of a medical device to...
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