DIN EN ISO 10524-2:2006-07
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
PRESSURE REGULATORS FOR USE WITH MEDICAL GASES - PART 2: MANIFOLD AND LINE PRESSURE REGULATORS
Hardcopy , PDF
04-09-2019
English
01-01-2006
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
National Annex NA (informative) Bibliography
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 DIN EN 738-2 E. (01/2007)
|
DocumentType |
Standard
|
Pages |
38
|
PublisherName |
German Institute for Standardisation (Deutsches Institut für Normung)
|
Status |
Superseded
|
SupersededBy |
Standards | Relationship |
UNE-EN ISO 10524-2:2007 | Identical |
BS EN ISO 10524-2:2006 | Identical |
NBN EN ISO 10524-2 : 2006 | Identical |
NF EN ISO 10524-2 : 2006 | Identical |
EN ISO 10524-2:2006 | Identical |
NEN EN ISO 10524-2 : 2006 | Identical |
EN ISO 10524-2:2019 | Identical |
NS EN ISO 10524-2 : 1ED 2006 | Identical |
UNI EN ISO 10524-2 : 2006 | Identical |
ISO 10524-2:2005 | Identical |
SN EN ISO 10524-2 : 2006 | Identical |
ONORM EN ISO 10524-2 : 2006 | Identical |
I.S. EN ISO 10524-2:2006 | Identical |
CGSB 24.2 : M86 | IDENTIFICATION OF MEDICAL GAS CONTAINERS, PIPELINES AND VALVES |
IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
ISO 15001:2010 | Anaesthetic and respiratory equipment Compatibility with oxygen |
EN 738-2 : 1998 | PRESSURE REGULATORS FOR USE WITH MEDICAL GASES - MANIFOLD AND LINE - PRESSURE REGULATORS |
ISO 4126-7:2013 | Safety devices for protection against excessive pressure — Part 7: Common data |
EN 737-3:1998/A1:1999 | MEDICAL GAS PIPELINE SYSTEMS - PIPELINES FOR COMPRESSED MEDICAL GASES AND VACUUM |
CGA C 9 : 2013 | STANDARD COLOR MARKING OF COMPRESSED GAS CONTAINERS FOR MEDICAL USE |
ISO 32:1977 | Gas cylinders for medical use — Marking for identification of content |
ISO 7291:2010 | Gas welding equipment Pressure regulators for manifold systems used in welding, cutting and allied processes up to 30 MPa (300 bar) |
ASTM G 175 : 2013 : REDLINE | Standard Test Method for Evaluating the Ignition Sensitivity and Fault Tolerance of Oxygen Pressure Regulators Used for Medical and Emergency Applications |
DIN EN ISO 10079-3:2000-03 | MEDICAL SUCTION EQUIPMENT - PART 3: SUCTION EQUIPMENT POWERED FROM A VACUUM OR POSITIVE PRESSURE GAS SOURCE (ISO 10079-3:2014) |
EN 1089-3:2011 | Transportable gas cylinders - Gas cylinder identification (excluding LPG) - Part 3: Colour coding |
ISO 10079-3:2014 | Medical suction equipment Part 3: Suction equipment powered from a vacuum or positive pressure gas source |
AS 2896-2011 | Medical gas systems - Installation and testing of non-flammable medical gas pipeline systems |
AS 4484:2016 | Gas cylinders for industrial, scientific, medical and refrigerant use - Labelling and colour coding |
ISO 14971:2007 | Medical devices Application of risk management to medical devices |
ISO 4135:2001 | Anaesthetic and respiratory equipment Vocabulary |
ISO 10524-1:2006 | Pressure regulators for use with medical gases Part 1: Pressure regulators and pressure regulators with flow-metering devices |
DIN EN ISO 4135:2002-03 | Anaesthetic and respiratory equipment - Vocabulary (ISO 4135:2001); Trilingual version EN ISO 4135:2001 |
ISO 7396-1:2016 | Medical gas pipeline systems — Part 1: Pipeline systems for compressed medical gases and vacuum |
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