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

published
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Organization: IEC - International Electrotechnical Commission
Publication Date: 5 October 2018
Status: published
Page Count: 52
ICS Code (Diagnostic equipment): 11.040.55
ICS Code (Electrical and electronic testing): 19.080
abstract:

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

Document History

October 5, 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 is also available as IEC 61010-2-101:2018 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the...
IEC 61010-2-101:2018 RLV
October 5, 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 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...
January 23, 2015
Safety requirements for electrical equipment for measurement, control and laboratory use – Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
IEC 61010-2-101:2015 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...
January 23, 2015
Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
IEC 61010-2-101:2015 is available as IEC 61010-2-101:2015 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous...
January 9, 2002
Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
Applies to equipment intended for in vitro diagnostic (IVD) medical purposes. This is used for the examination of specimens, including blood and tissue samples, derived from the human body. The...
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