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I.S. EN 737-3:1999

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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MEDICAL GAS PIPELINE SYSTEMS - PIPELINES FOR COMPRESSED MEDICAL GASES AND VACUUM

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

01-01-1999

Superseded date

28-05-2007

Superseded by

I.S. EN ISO 7396-1:2007

€149.00
Excluding VAT
Summarise this standard

For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.

Only cited Standards give presumption of conformance to New Approach Directives/Regulations.


Dates of withdrawal of national standards are available from NSAI.

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

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

DocumentType
Standard
Pages
114
PublisherName
National Standards Authority of Ireland
Status
Superseded
SupersededBy

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