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ONORM EN ISO 10524-2 : 2006

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

View Superseded by

PRESSURE REGULATORS FOR USE WITH MEDICAL GASES - PART 2: MANIFOLD AND LINE PRESSURE REGULATORS

Withdrawn date

15-07-2019

Published date

12-01-2013

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Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Symbols
5 General requirements
  5.1 Safety
  5.2 Alternative construction
  5.3 Materials
  5.4 Design requirements
  5.5 Constructional requirements
6 Test methods
  6.1 Conditions
  6.2 Test methods for manifold pressure regulators
  6.3 Test methods for line pressure regulators
  6.4 Test method for determination of the auto-ignition
      temperature of sealing materials and lubricants
  6.5 Test method for durability of markings and colour coding
7 Marking, colour coding, packaging
  7.1 Marking
  7.2 Colour coding
  7.3 Packaging
8 Information to be supplied by the manufacturer
Annex A (informative) Examples of pressure regulators
Annex B (informative) Rationale
Annex C (informative) Reported regional and national
        deviations of colour coding and nomenclature
        for medical gases
Annex ZA (informative) Relationship between this European
         Standard and the Essential Requirements of EU
         Directive 93/42/EEC Medical Devices
Bibliography

Provides requirements for manifold pressure regulators intended to be connected to cylinders with nominal filling pressures up to 25000 kPa at 15 degree C and for line pressure regulators for inlet pressures up to 3000 kPa.

DevelopmentNote
Supersedes ONORM EN 738-2. (11/2006)
DocumentType
Standard
PublisherName
Osterreichisches Normungsinstitut/Austrian Standards
Status
Withdrawn
SupersededBy

ONORM EN 13718-2 : 2015 MEDICAL VEHICLES AND THEIR EQUIPMENT - AIR AMBULANCES - PART 2: OPERATIONAL AND TECHNICAL REQUIREMENTS FOR AIR AMBULANCES

ISO 15001:2010 Anaesthetic and respiratory equipment Compatibility with oxygen
ISO 32:1977 Gas cylinders for medical use — Marking for identification of content
ISO 14971:2007 Medical devices Application of risk management to medical devices
ISO 7396-1:2016 Medical gas pipeline systems — Part 1: Pipeline systems for compressed medical gases and vacuum

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