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SRPS EN 60601-1-11:2016

Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment

Jan 29, 2016

General information

60.60     Jan 29, 2016

ISS

N062

European Norm

11.040.01     11.020.10  

English  

plan 2015

Buying

Published

Language in which you want to receive the document.

Scope

<span style='color:red'>NEW!</span> IEC 60601-1-11:2015 is available as <a href="http://webstore.iec.ch/webstore/webstore.nsf/Artnum_PK/9999962978?opendocument">IEC Standards+ 60601-1-11:2015 which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.


IEC 60601-1-11:201 5 applies to the basic safety and essential performance of medical electrical equipment and medical electrical systems for use in the home healthcare environment. It applies regardless of whether the medical electrical equipment or medical electrical system is intended for use by a lay operator or by trained healthcare personnel. The home healthcare environment includes:

- the dwelling place in which a patient lives;

- other places where patients are present both indoors and outdoors, excluding professional healthcare facility environments where operators with medical training are continually available when patients are present.

This second edition cancels and replaces the first edition of IEC 60601-1-11, published in 2010, and constitutes a technical revision. The most significant changes with respect to the previous edition include the following modifications:

- correction of test method for relative humidity control at temperatures above 35 °C;

- redrafting of subclauses that altered instead of adding to the general standard or other collateral standards; and

- harmonizing with the changes to the amendments to the general standard and other collateral standards.

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.

93/42/EEC

Medical devices

Life cycle

PREVIOUSLY

WITHDRAWN
SRPS EN 60601-1-11:2011

NOW

PUBLISHED
SRPS EN 60601-1-11:2016
60.60 Standard published
Jan 29, 2016

CORRIGENDA / AMENDMENTS

PUBLISHED
SRPS EN 60601-1-11:2016/A1:2021

Related project

Adopted from EN 60601-1-11:2015