BS EN 60601-2-26:2015
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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Medical electrical equipment Particular requirements for the basic safety and essential performance of electroencephalographs
Hardcopy , PDF
05-11-2021
English
30-06-2015
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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
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 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
Pertains to BASIC SAFETY and ESSENTIAL PERFORMANCE of ELECTROENCEPHALOGRAPHS (EEG) as defined in 201.3.63, hereafter referred to as ME EQUIPMENT.
| Committee |
CH/62/4
|
| DevelopmentNote |
Supersedes 01/564186 DC (08/2003) 2003 Edition remains active & will be withdrawn on 14/04/2018. Supersedes 09/30172488 DC. (06/2015) Supersedes BS 5724-2.126(1995). (08/2015)
|
| DocumentType |
Standard
|
| Pages |
36
|
| PublisherName |
British Standards Institution
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
IEC 60601-2-26:2012 standard applies to basic safety and essential performance of electroencephalographs used in a clinical environment (e.g., hospital, physician\'s office, etc.). This standard does not cover requirements for other equipment used in electroencephalography. This third edition cancels and replaces the second edition of IEC 60601-2-26 published in 2003. The aim of this third edition is to bring this particular standard up to date with reference to the third edition of the general standard IEC 60601-1:2005 Edition 3, through reformatting and technical changes.
| Standards | Relationship |
| DIN EN 60601-2-26 : 2016 | Identical |
| I.S. EN 60601-2-26:2015 | Identical |
| SN EN 60601-2-26 : 2003 | Identical |
| IEC 60601-2-26:2012 | Identical |
| EN 60601-2-26:2015 | Identical |
| NF EN 60601-2-26 : 2015 | Identical |
| UNE-EN 60601-2-26:2004 | Identical |
| EN 61308:2006 | Identical |
| IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
| EN 60601-2-27:2014 | Medical electrical equipment - Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment |
| 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 |
| IEC 60601-2-27:2011 | Medical electrical equipment - Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment |
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