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BS EN 60601-2-10:2015

Withdrawn
Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

Medical electrical equipment Particular requirements for the basic safety and essential performance of nerve and muscle stimulators
Amended by

BS EN 60601-2-10:2015+A1:2016

Available format(s)

Hardcopy , PDF

Withdrawn date

02-07-2020

Language(s)

English

Published date

06-30-2015

Publisher

British Standards Institution

FOREWORD
INTRODUCTION
201.1 Scope, object and related standards
201.2 Normative references
201.3 Terms and definitions
201.4 General requirements
201.5 General requirements for testing of ME
       EQUIPMENT
201.6 Classification of me equipment and ME
       SYSTEMS
201.7 Me EQUIPMENT identification, marking
       and documents
201.8 Protection against electrical HAZARDS from
       ME EQUIPMENT
201.9 Protection against MECHANICAL HAZARDS of ME EQUIPMENT
       and ME SYSTEMS
201.10 Protection against unwanted and excessive
       radiation HAZARDS
201.11 Protection against excessive temperatures and
       other HAZARDS
201.12 Accuracy of controls and instruments and
       protection against hazardous outputs
201.13 Hazardous situations and fault conditions
       for ME EQUIPMENT
201.14 PROGRAMMABLE ELECTRICAL
       MEDICAL SYSTEMS (PEMS)
201.15 Construction of ME EQUIPMENT
201.16 Me SYSTEMS
201.17 Electromagnetic compatibility of ME
       EQUIPMENT and ME SYSTEMS
202 Electromagnetic compatibility - Requirements and tests
Annexes
Annex C (informative) - Guide to marking and
        labelling requirements for ME EQUIPMENT
        AND ME SYSTEMS
Annex AA (informative) - Particular guidance and rationale
Index of defined terms used in this particular standard
Annex ZA (normative) - Normative references to
         international publications with their
         corresponding European publications
Annex ZZ (informative) - Coverage of Essential
         Requirements of EU Directives

Describes the requirements for the safety of nerve and Muscle STIMULATORS, defined in subclause 201.3.204, for use in the practice of physical medicine, hereinafter referred to as ME EQUIPMENT.

IEC 60601-2-10:2012 specifies the requirements for the safety and essential performance of nerve and muscle stimulators, for use in the practice of physical medicine. This includes transcutaneous electrical nerve stimulators (TENS) and electrical muscle stimulators (EMS). This second edition cancels and replaces the first edition, published in 1987 and its Amendment 1 (2001). This edition constitutes a technical revision and is aligned with IEC 60601-1:2005+A1:2012.

Committee
CH/62/4
DevelopmentNote
Supersedes and renumbers BS 5724-2.10(1988) (06/2001) Supersedes 84/52255 DC and 99/565079 DC. (04/2003) 2001 version incorporates amendment 13086 to BS 5724-2.10(1988). (04/2003) 2001 Edition along with its amendment remains active & will be withdrawn on 22/05/2018. Supersedes 10/30210946 DC & 15/30322732 DC. (06/2015) 2015 Edition remains active & will be withdrawn on 16/12/2019. 2015 Edition Re-issued in January 2017 & incorporates AMD 1 2016. (02/2017)
DocumentType
Standard
Pages
28
PublisherName
British Standards Institution
Status
Withdrawn
Supersedes

IEC 60601-1:2005+AMD1:2012 CSV Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
IEC 60601-1-2:2014 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
EN 60601-1-2:2015 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests

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Hardcopy - English
PDF - English
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