ONORM EN ISO 10524-2 : 2006
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
View Superseded by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
15-07-2019
12-01-2013
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Withdrawn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 |
Standards | Relationship |
NEN EN ISO 10524-2 : 2006 | Identical |
EN ISO 10524-2:2019 | Identical |
I.S. EN ISO 10524-2:2006 | Identical |
UNE-EN ISO 10524-2:2007 | Identical |
BS EN ISO 10524-2:2006 | Identical |
ISO 10524-2:2005 | Identical |
NF EN ISO 10524-2 : 2006 | Identical |
NBN EN ISO 10524-2 : 2006 | Identical |
NS EN ISO 10524-2 : 1ED 2006 | Identical |
UNI EN ISO 10524-2 : 2006 | Identical |
EN ISO 10524-2:2006 | Identical |
SN EN ISO 10524-2 : 2006 | Identical |
DIN EN ISO 10524-2:2006-07 | Identical |
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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