BS EN 1733:2002
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
Suction catheters for use in the respiratory tract
Hardcopy , PDF
29-08-2008
English
27-11-2002
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Foreword
Introduction
1 Scope
2 Normative references
3 Definitions
4 Size designation and dimensions
5 Materials
6 Design
7 Performance requirements
8 Requirements for suction catheters supplied sterile
9 Marking
Annex A (normative) Guidance on design and materials
Annex B (normative) Test method for security of
construction
Annex C (normative) Test method for residual vacuum
Bibliography
Gives requirements for suction catheters made of plastics materials and intended for use in suction of the respiratory tract. However, specialized suction catheters, for e.g. those with more than one lumen, are excluded from the scope of this standard.
| Committee |
CH/121/5
|
| DevelopmentNote |
Supersedes 01/561098 DC (12/2002) Supersedes BS 7213(1989) & 94/507818 DC. (03/2007)
|
| DocumentType |
Standard
|
| Pages |
20
|
| PublisherName |
British Standards Institution
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| I.S. EN 1733:2002 | Identical |
| EN 1733 : 2002 | Identical |
| UNE-EN 1733:2003 | Identical |
| NS EN 1733 : 2ED 2002 | Identical |
| NBN EN 1733 : 2003 | Identical |
| UNI EN 1733 : 2003 | Identical |
| NEN EN 1733 : 2002 | Identical |
| NF EN 1733 : 2003 | Identical |
| SN EN 1733 : 2003 | Identical |
| DIN EN 1733:2003-02 | Identical |
| ISO 8836:2014 | Suction catheters for use in the respiratory tract |
| EN 1282-1 : 1996 | ANAESTHETIC AND RESPIRATORY EQUIPMENT - TRACHEOSTOMY TUBES - TUBES FOR USE IN ADULTS |
| EN 1782:1998+A1:2009 | Tracheal tubes and connectors |
| EN 1282-2:2005+A1:2009 | Tracheostomy tubes - Part 2: Paediatric tubes (ISO 5366-3:2001, modified) |
| EN 868-1 : 1997 | PACKAGING MATERIALS AND SYSTEMS FOR MEDICAL DEVICES WHICH ARE TO BE STERILIZED - GENERAL REQUIREMENTS AND TEST METHODS |
| EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
| ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
| ISO/TR 11991:1995 | Guidance on airway management during laser surgery of upper airway |
| ISO 7000:2014 | Graphical symbols for use on equipment Registered symbols |
| ISO 4135:2001 | Anaesthetic and respiratory equipment Vocabulary |
| EN ISO 4135:2001 | Anaesthetic and respiratory equipment - Vocabulary (ISO 4135:2001) |
| EN 980:2008 | Symbols for use in the labelling of medical devices |
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