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BS EN 1782 : 1998

BS EN 1782 : 1998

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by

TRACHEAL TUBES AND CONNECTORS

Amended by

BS EN 1782:1998+A1:2009

Available format(s)

Hardcopy , PDF

Superseded date

30-04-2014

Superseded by

BS EN ISO 5361:2016

Language(s)

English

Published date

01-01-1998

Publisher

British Standards Institution

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Hardcopy - English
PDF - English
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Foreword
Introduction
1 Scope
2 Normative references
3 Definitions
4 General requirements for tracheal tubes
  and tracheal tube connectors
5 Additional requirements for tracheal tubes
  with a Murphy eye
6 Requirements for tracheal tubes and tracheal
  tube connectors supplied sterile
7 Marking
Annex A (normative) - Test method for determining
                      the resting diameter of the cuff
Annex B (normative) - Test method for tube collapse
Annex C (normative) - Test method for cuff herniation
Annex D (informative) - Guidance on materials and design
Annex E (informative) - Bibliography
Annex ZA (informative) - Relationship between this
                         European Standard and the
                         Essential Requirements of
                         EU Directive 93/42/EEC

Defines requirements for oro-tracheal and naso-tracheal tubes (plain and cuffed) made from plastics materials and/or rubber and requirements for tracheal tube connectors.

Committee
CH/121/5
DevelopmentNote
Supersedes 95/560036 DC, BS 3487-1(1989), BS 3487-2(1993), BS 3487-3(1986), BS 3487-5(1986) and BS 6546(1994) (08/2004) 1998 Edition Re-Issued in December 2009 & incorporates AMD 1 2009. Supersedes 09/30186950 DC. (12/2009)
DocumentType
Standard
Pages
36
PublisherName
British Standards Institution
Status
Superseded
SupersededBy
Supersedes

BS 6155:1990 Specification for tracheal tubes for large animals in veterinary anaesthesia

EN 556:1994 + A1:1998 STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR TERMINALLY-STERILIZED MEDICAL DEVICES TO BE LABELLED "STERILE"
IEC 60601-1-6:2010+AMD1:2013 CSV Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability
EN 868-1 : 1997 PACKAGING MATERIALS AND SYSTEMS FOR MEDICAL DEVICES WHICH ARE TO BE STERILIZED - GENERAL REQUIREMENTS AND TEST METHODS
EN 60601-1-6:2010/A1:2015 MEDICAL ELECTRICAL EQUIPMENT - PART 1-6: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: USABILITY (IEC 60601-1-6:2010/A1:2013)
IEC 62366:2007+AMD1:2014 CSV Medical devices - Application of usability engineering to medical devices
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
EN 62366 : 2008 AMD 1 2015 MEDICAL DEVICES - APPLICATION OF USABILITY ENGINEERING TO MEDICAL DEVICES (IEC 62366:2007/A1:2014)
EN 1281-1:1997/A1:1998 ANAESTHETIC AND RESPIRATORY EQUIPMENT - CONICAL CONNECTORS - CONES AND SOCKETS
ISO/TR 11991:1995 Guidance on airway management during laser surgery of upper airway
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
ISO 594-1:1986 Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment Part 1: General requirements
EN 30993-1 : 1994 BIOLOGICAL EVALUATION OF MEDICAL DEVICES - GUIDANCE ON SELECTION OF TESTS

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