BS EN 60601-2-40:1998
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
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Medical electrical equipment. Particular requirements for safety Specification for electromyographs and evoked response equipment
Hardcopy , PDF
27-01-2022
English
15-06-1998
Committee |
CH/62/4
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DevelopmentNote |
Also numbered as BS 5724-2.40(1998) & IEC 60601-2-40. Supersedes 95/562289 DC. To be read in conjunction with BS EN 60601-1. (11/2005)
|
DocumentType |
Standard
|
Pages |
16
|
PublisherName |
British Standards Institution
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Status |
Withdrawn
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SupersededBy | |
Supersedes |
This clause of the General Standard applies except as follows: 1.1 Scope Addition: This Particular Standard applies to electromyographs as defined in 2.1.101 and evoked response equipment as defined in 2.1.102, hereinafter referred to as equipment. 1.2 Object Replacement: The object of this Particular Standard is to establish particular requirements for the safety of electromyographs and evoked response equipment as defined in 2.1.101 and 2.1.102, respectively. 1.3 Particular Standards Addition: This Particular Standard refers to IEC60601-1 (1988): Medical electrical equipment— Part1: General requirements for safety as amended by its amendment 1 (1991) and amendment 2 (1995). For brevity, IEC60601-1 is referred to in this Particular Standard either as the \'General Standard\' or as the \'General Requirement(s)\'. The numbering of sections, clauses and subclauses of this Particular Standard corresponds to that of the General Standard. The changes to the text of the General Standard are specified by the use of the following words: \'Replacement\' means that the clause or subclause of the General Standard is replaced completely by the text of this Particular Standard. \'Addition\' means that the text of the Particular Standard is additional to the requirements of the General Standard. \'Amendment\' means that the clause or subclause of the General Standard is amended as indicated by the text of this Particular Standard. Subclauses or figures which are additional to those of the General Standard are numbered starting from 101, additional annexes are lettered AA, BB, etc., and additional items aa), bb), etc. The term \'this Standard\' is used to make references to the General Standard and this Particular Standard taken together. Where there is no corresponding section, clause or subclause in this Particular Standard, the section, clause or subclause of the General Standard, although possibly not relevant, applies without modification; where it is intended that any part of the General Standard, although possibly relevant, is not to be applied, a statement to that effect is given in this Particular Standard. The requirements of this Particular Standard take priority over those of the General Standard. 1.5 Collateral Standards Addition: Collateral Standards IEC60601-1-1 as amended by its amendment 1 and IEC60601-1-2 have been taken into consideration in this Particular Standard (see 6.8.2 and clause 36).
Standards | Relationship |
DIN EN 60601-2-40 : 1998 | Identical |
UNE-EN 60601-2-40:1999 | Identical |
IEC 60601-2-40:1998 | Identical |
SN EN 60601-2-40 : 1998 | Identical |
I.S. EN 60601-2-40:1999 | Identical |
NF EN 60601-2-40 : 2000 | Identical |
EN 60601-2-40:1998 | Identical |
EN 60645-3:2007 | Electroacoustics - Audiometric equipment - Part 3: Test signals of short duration |
IEC 60645-3:2007 | Electroacoustics - Audiometric equipment - Part 3: Test signals of short duration |
EN 60825-1:2014/AC:2017-06 | SAFETY OF LASER PRODUCTS - PART 1: EQUIPMENT CLASSIFICATION AND REQUIREMENTS (IEC 60825-1:2014) |
IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
IEC 60825-1:2014 | Safety of laser products - Part 1: Equipment classification and requirements |
EN 60601-1-1:2001 | Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems |
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 60601-1-1:2000 | Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems |
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