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DIN EN ISO 7396-1:2016-09

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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 - PART 1: PIPELINE SYSTEMS FOR COMPRESSED MEDICAL GASES AND VACUUM (ISO 7396-1:2016)

Available format(s)

Hardcopy , PDF

Language(s)

German, English

Published date

01-09-2016

Superseded date

31-05-2019

€394.28
Excluding VAT
Summarise this standard

National foreword
National Annex NA (informative) - Bibliography
European foreword
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 and commissioning
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 documenting compliance
        of the 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
Annex K (informative) - Manufacture of medical gases on site,
        Responsibility for medical gas quality
Bibliography
Annex ZA (informative) - Relationship between this
         European Standard and the Essential
         Requirements of EU Directive 93/42/EEC
         on Medical devices

Defines requirements for design, installation, function, performance, testing, commissioning and documentation of pipeline systems used in healthcare facilities.

DevelopmentNote
Supersedes DIN EN 737-3. (07/2007) Supersedes DIN ISO 10083. (09/2016) DRAFT AMD 1 issued in April 2017. (04/2017)
DocumentType
Standard
Pages
206
PublisherName
German Institute for Standardisation (Deutsches Institut für Normung)
Status
Superseded
SupersededBy
Supersedes

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A newer version of this standard is available.

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€394.28
Excluding VAT