EN 737-3:1998/A1:1999

Foreword
Introduction
1 Scope
2 Normative References
3 Definitions
4 General Requirements
5 Source of Supply
6 Monitoring and alarm systems
7 Pipelines
8 Shut-off valves
9 Terminal units, gas-specific connectors and medical
   supply units
10 Marking and colour coding
11 Pipeline installation
12 Testing, commissioning and certification
13 Information to be supplied by the manufacturer
Annexes
ANNEX A (Informative) Schematic representation of
         sources of supply
ANNEX B (Informative) Guidelines for location of
         cylinder manifolds and stationary cryogenic
         vessels
ANNEX C (Informative) Procedure for testing and
         commissioning
ANNEX D (Informative) Temperature and pressure
         relationships
ANNEX E (Informative) Method for measuring pipeline
         volume
ANNEX F (Informative) Guidelines for general requirements
         for supply plants
ANNEX G (Informative) Guidelines for emergency procedures
ANNEX H (Informative) Recommended minimum requirements
         for the organization of the maintenance
ANNEX J (Informative) Typical forms for certification of
         the pipeline systems
ANNEX K (Informative) Bibliography
ANNEX L (Informative) Rationale
Annex ZA (informative) Clauses of this European Standard
         addressing Essential Requirements or other
         provisions of EU Directives

Defines basic requirements for installation, function, performance, documentation, testing and commissioning of compressed medical gases and vacuum pipeline systems for ensuring patient safety by continuous delivering of the correct gas from the pipeline system.