Active standard | Published: 01/04/2023

ČSN EN IEC 61010-2-101-ed.3

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

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Detail information

Designation: ČSN EN IEC 61010-2-101-ed.3

Publication date: 01/04/2023

Pages: 24

Country: Czech technical standard

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Anotation

This part of IEC 61010 applies to equipment intended for in vitro diagnostic (IVD) medical purposes, including self-test IVD medical purposes.
IVD medical equipment, whether used alone or in combination, is intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue samples, derived from the human body, solely or principally for the purpose of providing information concerning one or more of the following:
- a physiological or pathological state; or
- a congenital abnormality;
- the determination of safety and compatibility with potential recipients;
- the monitoring of therapeutic measures.
Self-test IVD medical equipment is intended by the manufacturer for use by lay persons in a home environment
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