BS EN ISO 5359:2014+A1:2017:2018 Edition
$167.15
Anaesthetic and respiratory equipment. Low-pressure hose assemblies for use with medical gases
Published By | Publication Date | Number of Pages |
BSI | 2018 | 36 |
1.1 This International Standard specifies requirements for low-pressure hose assemblies intended for use with the following medical gases:
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oxygen,
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nitrous oxide,
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medical air,
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helium,
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carbon dioxide,
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xenon,
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specified mixtures of the gases listed above,
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oxygen 93 ,
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air for driving surgical tools,
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nitrogen for driving surgical tools,
and for use with vacuum.
1.2 *It applies to hose assemblies operating at pressures up to 1 400 kPa and for vacuum systems at pressures not greater than 60 kPa absolute.
1.3 This International Standard does not specify the dimensions and allocation of the gas-specific inlet and outlet connectors for the hose assemblies.
NOTE 1 Specifications for the dimensions and allocation of diameter index safety system (DISS) connectors are specified in CGA V‑5 [28].
NOTE 2 Specifications for the dimensions and allocation of sleeve indexed system (SIS) connectors are specified in AS 2896 [23].
NOTE 3 Dimensions and allocation of non-interchangeable screw-threaded (NIST) connectors are specified in ISO 18082 [11].
NOTE 4 Terminal units designed for quick connectors are specified in ISO 9170‑1 .
1.4 This International Standard does not specify requirements for coaxial hoses used for the supply and removal of air for driving surgical tools.
1.5 This International Standard does not specify the intended uses of hose assemblies.
NOTE Environmental aspects are dealt with in Annex B.
PDF Catalog
PDF Pages | PDF Title |
---|---|
2 | National foreword |
4 | European foreword |
5 | Foreword to Amendment A1 Foreword to Amendment A1 |
6 | Annex ZA (informative) Relationship between this European Standard and the essential requirements of Directive 93/42/EEC [OJ L 169] aimed to be covered |
10 | Foreword |
11 | Introduction |
13 | 1 Scope |
14 | 2 Normative references 3 Terms and definitions |
18 | 4 General requirements 4.1 Risk management 4.2 Usability 4.3 Clinical investigation 4.4 Safety |
19 | 4.5 Materials 4.6 Design requirements 4.6.1 Hose internal diameter |
20 | 4.6.2 Mechanical strength 4.6.3 Deformation under pressure 4.6.4 Resistance to occlusion 4.6.5 Adhesion strength |
21 | 4.6.6 Flexibility 4.6.7 Gas specificity 4.6.8 End connectors 4.6.9 Joining hoses to hose inserts |
22 | 4.6.10 Leakage 4.6.11 *Pressure drop 4.7 Constructional requirements 4.7.1 Cleaning 4.7.2 Lubricants |
23 | 5 Test methods 5.1 General 5.1.1 Ambient conditions 5.1.2 Test gas 5.1.3 Reference conditions 5.2 Test method for pressure drop 5.3 Test method for leakage 5.3.1 For all hose assemblies 5.3.2 For hose assemblies fitted with a hose assembly check valve 5.4 Test method for gas specificity 5.5 Test method for mechanical strength |
24 | 5.6 Test method for deformation under pressure 5.7 Test method for resistance to occlusion |
25 | 5.8 Test method for durability of markings and colour coding 6 Marking, colour coding and packaging 6.1 Marking |
26 | 6.2 Colour coding |
27 | 6.3 Packaging 7 Information to be supplied by the manufacturer |
29 | Annex A (informative) Rationale |
30 | Annex B (informative) Environmental aspects |
31 | Annex C (informative) Reported regional and national deviations of colour coding and nomenclature for medical gases |
33 | Bibliography |