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Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
5 Supply systems
6 Monitoring and alarm systems
7 Pipeline distribution systems
8 Shut-off valves
9 Terminal units, gas-specific connectors, medical supply
   units, pressure regulators and pressure gauges
10 Marking and colour coding
11 Pipeline installation
12 Testing, commissioning and certification
13 Information to be supplied by the manufacturer
Annex A (informative) - Schematic representations of typical
        supply systems and area distribution systems
Annex B (informative) - Guidelines for location of cylinder
        manifolds, cylinder storage areas and stationary vessels
        for cryogenic or non-cryogenic liquids
Annex C (informative) - Example of procedure for testing and
        commissioning
Annex D (informative) - Typical forms for certification of
        pipeline systems for compressed medical gas and
        vacuum
Annex E (informative) - Temperature and pressure relationships
Annex F (informative) - Risk management checklist
Annex G (informative) - Operational management
Annex H (informative) - Rationale
ANNEX I (informative) - Rationale for compressor hazards
Annex J (informative) - Considerations for implementation and
        use of oxygen 93 and oxygen 90+
Annex K (informative) - Manufacture of medical gases on
        site - Responsibility for medical gas quality
Annex L - Bibliography
Annex ZA (informative) - Relationship between this European
         Standard and the Essential Requirements of EU
         Directive 93/42/EEC Medical Devices

BS EN ISO 7396-1