DIN EN 1782:2009-12
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by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
Hardcopy , PDF
03-01-2013
English
01-01-2009
Important note : All end users must be registered with an Account prior to user licenses being assigned.
Vorwort
Einleitung
1 Anwendungsbereich
2 Normative Verweisungen
3 Begriffe
4 Allgemeine Anforderungen an Trachealtuben und
an Verbindungsstücke für Trachealtuben
5 Zusätzliche Anforderungen an Trachealtuben mit
Murphy-Auge
6 Anforderungen an steril gelieferte Trachealtuben und
Verbindungsstücke
7 Kennzeichnung
Anhang A (normativ) Bestimmung des Durchmessers
des gefüllten, jedoch nicht gedehnten Cuffs
Anhang B (normativ) Prüfung auf Lumeneinschränkung
Anhang C (normativ) Prüfung auf Cuffhernienbildung
Anhang D (informativ) Leitfaden für Werkstoffe und
Ausführung
Anhang E (informativ) Literaturhinweise
Anhang ZA (informativ) Zusammenhang zwischen dieser
Europäischen Norm und den grundlegenden
Anforderungen der EG-Richtlinie 93/42/EWG
Das Dokument legt Anforderungen an Oro- und Naso-Trachealtuben (mit und ohne Cuff) aus Kunststoffen und/oder Gummi sowie Anforderungen an Verbindungsstücke für Trachealtuben fest.
| DevelopmentNote |
Supersedes DIN ISO 5361-1, -2, -3, -5 and DIN ISO 7228. (08/2002)
|
| DocumentType |
Standard
|
| Pages |
38
|
| PublisherName |
German Institute for Standardisation (Deutsches Institut für Normung)
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| NEN EN 1782 : 1998 + A1 2009 | Identical |
| I.S. EN 1782:1998 | Identical |
| UNI EN 1782 : 2009 | Identical |
| NF EN 1782 : 1998 + A1 2009 | Identical |
| UNE-EN 1782:1998 | Identical |
| EN 1782:1998+A1:2009 | Identical |
| NS EN 1782 : 1998 + A1 2009 | Identical |
| BS EN 1782 : 1998 | Identical |
| NBN EN 1782 : 1998 + A1 2009 | Identical |
| SN EN 1782 : 1998 + A1 2010 | Identical |
| 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 |
Access your standards online with a subscription
Features
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.