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BS EN 1733:2002

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by
superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

Suction catheters for use in the respiratory tract

Available format(s)

Hardcopy , PDF

Superseded date

08-29-2008

Language(s)

English

Published date

11-27-2002

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Superseded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
EN 980:2008 Symbols for use in the labelling of medical devices
EN ISO 10993-1:2009/AC:2010 BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 1: EVALUATION AND TESTING WITHIN A RISK MANAGEMENT PROCESS (ISO 10993-1:2009/COR 1:2010)

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