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SRPS EN 61010-2-101:2009

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

Apr 27, 2009
95.99   Withdrawal of Standard   Jul 31, 2020

General information

95.99     Jul 31, 2020

ISS

N045

European Norm

11.040.55     19.080  

English  

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Scope

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 standard also covers self-test IVD medical equipment for use by lay persons.

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

98/79/EC

In vitro diagnostic medical devices

Harmonized

Life cycle

NOW

WITHDRAWN
SRPS EN 61010-2-101:2009
95.99 Withdrawal of Standard
Jul 31, 2020

REVISED BY

PUBLISHED
SRPS EN 61010-2-101:2017

Related project

Adopted from EN 61010-2-101:2002