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EN 1251-3:2000

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by

Cryogenic vessels - Transportable vacuum insulated vessels of not more than 1000 litres volume - Part 3: Operational requirements

Superseded date

01-09-2015

Superseded by

EN ISO 21029-2:2015

Published date

19-01-2000

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Foreword
1 Scope
2 Normative references
3 Definitions
4 Preliminaries before putting into service
5 Personnel training
6 General safety requirements
7 Putting into service
8 Location
9 Transport within the location
10 Filling
11 Product withdrawal
12 Change of service
13 Taking out of service
14 Maintenance and repair
15 Periodic inspection
16 Additional requirements for flammable gases
17 Emergency equipment/procedures
Annex A (informative) - Example of an emergency procedure
Annex B (informative) - Safety distance
Annex C (informative) - Qualification of existing national
        small transportable cryogenic vessels for use in
        the European union
Annex D (informative) - A-deviations

This European Standard specifies operational requirements for transportable vacuum insulated cryogenic vessels of not more than 1000 litres volume designed to operate above atmospheric pressure. Appropriate parts may be used as a guidance for a vessel design to operate open to the atmosphere. For small cryogenic vessels specially designed for personal medical use, this standard can be used as a guide only.

Committee
CEN/TC 268
DocumentType
Standard
PublisherName
Comite Europeen de Normalisation
Status
Superseded
SupersededBy

Standards Relationship
UNI EN 1251-3 : 2002 Identical
NBN EN 1251-3 : 2000 Identical
BS EN 1251-3:2000 Identical
NS EN 1251-3 : 1ED 2000 Identical
I.S. EN 1251-3:2000 Identical
NEN EN 1251-3 : 2000 Identical
NF EN 1251-3 : 2000 Identical
PN EN 1251-3 : 2002 Identical
UNE-EN 1251-3:2001 Identical
SN EN 1251-3 : 2000 Identical
DIN EN 1251-3:2000-03 Identical

I.S. EN ISO 18777:2009 TRANSPORTABLE LIQUID OXYGEN SYSTEMS FOR MEDICAL USE - PARTICULAR REQUIREMENTS
EN 1251-1:2000 Cryogenic vessels - Transportable vacuum insulated vessels of not more than 1000 litres volume - Part 1: Fundamental requirements
DIN ISO 13022 E : 2014 MEDICAL PRODUCTS CONTAINING VIABLE HUMAN CELLS - APPLICATION OF RISK MANAGEMENT AND REQUIREMENTS FOR PROCESSING PRACTICES (ISO 13022:2012)
DIN EN ISO 18777:2009-07 TRANSPORTABLE LIQUID OXYGEN SYSTEMS FOR MEDICAL USE - PARTICULAR REQUIREMENTS
DIN ISO 13022:2014-06 MEDICAL PRODUCTS CONTAINING VIABLE HUMAN CELLS - APPLICATION OF RISK MANAGEMENT AND REQUIREMENTS FOR PROCESSING PRACTICES (ISO 13022:2012)
BS EN 1251-1:2000 Cryogenic vessels. Transportable vacuum insulated vessels of not more than 1000 litres volume Fundamental requirements
UNI EN ISO 18777 : 2009 TRANSPORTABLE LIQUID OXYGEN SYSTEMS FOR MEDICAL USE - PARTICULAR REQUIREMENTS
ISO 13022:2012 Medical products containing viable human cells — Application of risk management and requirements for processing practices
ISO 18777:2005 Transportable liquid oxygen systems for medical use — Particular requirements
EN ISO 18777:2009 Transportable liquid oxygen systems for medical use - Particular requirements (ISO 18777:2005)
10/30203224 DC : 0 BS ISO 13022 - MEDICAL PRODUCTS CONTAINING VIABLE HUMAN CELLS - APPLICATION OF RISK MANAGEMENT AND REQUIREMENTS FOR PROCESSING PRACTICES
ANSI/AAMI/ISO 13022:2012 MEDICAL PRODUCTS CONTAINING VIABLE HUMAN CELLS - APPLICATION OF RISK MANAGEMENT AND REQUIREMENTS FOR PROCESSING PRACTICES
BS EN 1251-2:2000 Cryogenic vessels. Transportable vacuum insulated vessels of not more than 1000 litres volume Design, fabrication, inspection and testing
BS EN ISO 18777:2009 Transportable liquid oxygen systems for medical use. Particular requirements

EN 12300 : 1998 AMD 1 2006 CRYOGENIC VESSELS - CLEANLINESS FOR CRYOGENIC SERVICE
EN 1251-1:2000 Cryogenic vessels - Transportable vacuum insulated vessels of not more than 1000 litres volume - Part 1: Fundamental requirements

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