EN 1251-3:2000
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by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
01-09-2015
19-01-2000
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Superseded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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