EN 60601-2-40:1998
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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 - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment
18-01-2019
14-04-1998
INTRODUCTION
SECTION ONE: GENERAL
1 Scope and object
2 Terminology and definitions
5 Classification
6 Identification, marking and documents
7 Power input
SECTION TWO: ENVIRONMENTAL CONDITIONS
SECTION THREE: PROTECTION AGAINST ELECTRIC SHOCK HAZARDS
14 Requirements related to classification
20 Dielectric strength
SECTION FOUR: PROTECTION AGAINST MECHANICAL HAZARDS
SECTION FIVE: PROTECTION AGAINST HAZARDS FROM UNWANTED OR
EXCESSIVE RADIATION
36 Electromagnetic compatibility
SECTION SIX: PROTECTION AGAINST HAZARDS OF IGNITION OF
FLAMMABLE ANAESTHETIC MIXTURES
SECTION SEVEN: PROTECTION AGAINST EXCESSIVE TEMPERATURES AND
OTHER SAFETY HAZARDS
42 Excessive temperatures
46 Human errors
SECTION EIGHT: ACCURACY OF OPERATING DATA AND PROTECTION
AGAINST HAZARDOUS OUTPUT
50 Accuracy of operating data
51 Protection against hazardous output
SECTION NINE: ABNORMAL OPERATION AND FAULT CONDITIONS:
ENVIRONMENTAL TESTS
SECTION TEN: CONSTRUCTIONAL REQUIREMENTS
Figure 101
Annexes
L - References - Publications mentioned in this Standard
AA (informative) - General guidance and rationale
ZA Normative references to international publications with
their corresponding European publications
Establishes particular requirements for the safety of electromyographs and evoked response equipment as defined in clause 2 of this standard.
Committee |
CLC/TC 62
|
DevelopmentNote |
To be read in conjunction with EN 60601-1:1990 and EN 60601-1-1:1993 (05/2001)
|
DocumentType |
Standard
|
PublisherName |
European Committee for Standards - Electrical
|
Status |
Superseded
|
SupersededBy |
Standards | Relationship |
SN EN 60601-2-40 : 1998 | Identical |
IEC 60601-2-40:2016 | Identical |
I.S. EN 60601-2-40:1999 | Identical |
BS EN 60601-2-40:1998 | Identical |
PN EN 60601-2-40 : 2005 | Identical |
NF EN 60601-2-40 : 2000 | Identical |
NEN EN IEC 60601-2-40 : 2003 | Identical |
BS 5724-2.40(1998) : 1998 | Identical |
UNE-EN 60601-2-40:1999 | Identical |
NBN EN 60601 2-40 : 1998 | Identical |
VDE 0750-2-40 : 1998 | Identical |
CEI EN 60601-2-40 : 1999 | Identical |
ONORM OVE EN 60601-2-40 : 1998 | Identical |
DIN EN 60601-2-40 : 1998 | Identical |
UNE-EN 60645-7:2010 | Electroacoustics - Audiometric equipment -- Part 7: Instruments for the measurement of auditory brainstem responses |
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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