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02/564924 DC : DRAFT NOV 2002

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

ISO 21647 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-55: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS
Superseded date

12-06-2004

Published date

11-23-2012

1 Scope
2 Normative reference(s)
3 Term(s) and definition(s)
4 General requirements and general requirements for
    tests
    4.101 Other test methods
    4.102 Acceptance criteria
5 Classification
6 Identification, marking and documents
    6.1 Marking on the outside of EQUIPMENT or
          EQUIPMENT parts
    6.3 Markings of controls and instruments
    6.8 ACCOMPANYING DOCUMENTS
          6.8.2 Instructions for use
    6.101 Test method of legibility
7 Power input
8 Basic safety categories
9 Removable protective means
10 Environmental conditions
11 Not used
12 Not used
13 General
14 Requirements related to classification
15 Limitation of voltage and/or energy
16 ENCLOSURES and PROTECTIVE COVERS
17 Separation
18 Protective earthing, functional earthing and
    potential equalization
19 Continuous LEAKAGE CURRENTS and PATIENT AUXILIARY
    CURRENTS
20 Dielectric strength
21 Mechanical strength
    21.101 Shock and vibration
    21.102 Shock and vibration for transport
22 Moving parts
23 Surfaces, corners and edges
24 Stability in NORMAL USE
25 Expelled parts
26 Vibration and noise
27 Pneumatic and hydraulic power
28 Suspended masses
29 X-Radiation
30 Alpha, beta, gamma, neutron radiation and other
    particle radiation
31 Microwave radiation
32 Light radiation (including lasers)
33 Infra-red radiation
34 Ultraviolet energy
35 Acoustical energy (including ultrasonics)
36 Electromagnetic Compatibility
37 Locations and basic requirements
38 Marking and ACCOMPANYING DOCUMENTS
39 Common requirements for CATEGORY AP AND CATEGORY APG
    EQUIPMENT
40 Requirements and tests for CATEGORY AP EQUIPMENT,
    parts and components thereof
41 Requirements and tests for CATEGORY APG EQUIPMENT,
    parts and components thereof
42 Excessive temperatures
43 Fire prevention
    43.101 RGM used in conjunction oxidants
44 Overflow, spillage, leakage, humidity, ingress of
    liquids, cleaning, sterilization, disinfection and
    compatibility
    44.3 Spillage
    44.7 Cleaning, sterilization and disinfection
    44.8 Compatibility with substances used with the
           EQUIPMENT
45 Pressure vessels and parts subject to PRESSURE
46 Human errors
47 Electrostatic charges
48 Biocompatibility
49 Interruption of the power supply
    49.101 Primary electrical (AC or DC) power source -
           External
           49.101.1 External - No reserve electrical power
                    source
           49.101.2 External - With reserve electrical power
                    source
    49.102 Primary electrical power source - Internal
           49.102.1 Internal - No reserve electrical power
                    source
           49.102.2 Internal - With a reserve electrical
                    power source
    49.104 RESERVE ELECTRICAL POWER SOURCE minimum operating
           time
    49.105 RESERVE ELECTRICAL POWER SOURCE for use outside the
           healthcare facility
50 Accuracy of operating data
51 Protection against hazardous output
    51.101 MEASUREMENT ACCURACY
           51.101.1 General
           51.101.2 DRIFT of MEASUREMENT ACCURACY
           51.101.3 MEASUREMENT ACCURACY of GAS READINGS for
                    gas mixtures
    51.102 TOTAL SYSTEM RESPONSE TIME
    51.103 Indication of GAS READINGS units of measure
    51.104 Indication of operating mode
52 Abnormal operation and fault conditions
53 Environmental tests
54 General
55 ENCLOSURES and covers
56 Components and general assembly
    56.7 Batteries
57 MAINS PARTS, components and layout
    57.3 POWER SUPPLY CORDS
58 Protective earthing - Terminals and connections
59 Construction and layout
101 Additional Requirements Specifically Related of
    RESPIRATORY GAS MONITORS
    101.1 Interfering Gas and vapor effects
    101.2 Gas Leakage
    101.3 Sample Gas Exhaust Port
    101.4 Minimum Sampling Flow
    101.5 Contamination of Breathing Systems
201 ALARM SYSTEMS
          201.3.2 ALARM PRESETS
          201.4.2 Adjustable ALARM LIMITS
    201.6 ALARM SIGNAL ANNUNCIATION inactivation states
          201.6.3 Indication and access
Tables
Figures
Appendices and Annexes
Annexes
Annex AA Rationale (Informative)
Annex ZA Reference to the Essential Principles (Informative)
Bibliography
Terminology - Index of defined terms

Committee
CH/121/1
DocumentType
Draft
PublisherName
British Standards Institution
Status
Superseded
SupersededBy

IEC 60950:1999 Safety of information technology equipment
IEC 60601-1:2005+AMD1:2012 CSV Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
EN 12598 : 1999 OXYGEN MONITORS FOR PATIENT BREATHING MIXTURES - PARTICULAR REQUIREMENTS
ISO 7767:1997 Oxygen monitors for monitoring patient breathing mixtures — Safety requirements
ISO 9918:1993 Capnometers for use with humans Requirements
EN 864 : 1996 MEDICAL ELECTRICAL EQUIPMENT - CAPNOMETERS FOR USE WITH HUMANS - PARTICULAR REQUIREMENTS
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
ISO/TR 16142:2006 Medical devices Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices
NFPA 53M : 1990 FIRE HAZARDS IN OXYGEN-ENRICHED ATMOSPHERES
EN ISO 11196 : 1997 ANAESTHETIC GAS MONITORS
ISO 14971:2007 Medical devices Application of risk management to medical devices
ISO 7000:2014 Graphical symbols for use on equipment Registered symbols
ISO 4135:2001 Anaesthetic and respiratory equipment Vocabulary
IEC 60601-1-1:2000 Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems
IEC 60601-1-4:1996+AMD1:1999 CSV Medical electrical equipment - Part 1-4: General requirements for safety - Collateral Standard: Programmable electrical medical systems
ISO 15223:2000 Medical devices Symbols to be used with medical device labels, labelling and information to be supplied

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