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DIN EN 1282-2:2009-12

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by

TRACHEOSTOMY TUBES - PART 2: PAEDIATRIC TUBES

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

01-01-2009

Superseded date

01-04-2017

Vorwort
Einleitung
1 Anwendungsbereich
2 Normative Verweisungen
3 Begriffe
4 Grössen und Masse
5 Werkstoffe
6 Ausführung
7 Anforderungen an steril gelieferte Tracheotomietuben
8 Kennzeichnung
9 Adapter
Anhang A (normativ) Prüfung der sicheren Befestigung
          eines dauerhaft angebrachten Verbindungsstücks,
          soweit vorhanden, und der Halsplatte am
          Tracheotomietubus
Anhang B (normativ) Bestimmung des Durchmessers des
          gefüllten, jedoch nicht gedehnten Cuffs
Anhang C (informativ) Leitfaden für Werkstoffe und
          Ausführung
Anhang ZA (informativ) Zusammenhang zwischen dieser
          Europäischen Norm und den grundlegenden
          Anforderungen der EG-Richtlinie 93/42/EWG
Literaturhinweise

Dieses Dokument legt Anforderungen an pädiatrische Trachetomietuben aus Kunststoffen und/oder Gummi mit einem Innendurchmesser von 2,0 mm bis 6,0 mm fest.

DevelopmentNote
Supersedes DIN EN ISO 5366-3 issue 12-2003. (09/2005)
DocumentType
Standard
Pages
22
PublisherName
German Institute for Standardisation (Deutsches Institut für Normung)
Status
Superseded
SupersededBy

EN ISO 5356-1:2015 Anaesthetic and respiratory equipment - Conical connectors - Part 1: Cones and sockets (ISO 5356-1:2015)
ISO 5356-1:2015 Anaesthetic and respiratory equipment — Conical connectors — Part 1: Cones and sockets
EN 1041:2008+A1:2013 Information supplied by the manufacturer of medical devices
ISO 5366-1:2000 Anaesthetic and respiratory equipment — Tracheostomy tubes — Part 1: Tubes and connectors for use in adults
EN ISO 5366-1:2009 Anaesthetic and respiratory equipment - Tracheostomy tubes - Part 1: Tubes and connectors for use in adults (ISO 5366-1:2000)
ISO 10993-1:2009 Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process
ISO 11607:2003 Packaging for terminally sterilized medical devices
ISO 5361:2016 Anaesthetic and respiratory equipment — Tracheal tubes and connectors
ISO/TR 11991:1995 Guidance on airway management during laser surgery of upper airway
ISO 4135:2001 Anaesthetic and respiratory equipment — Vocabulary
EN 980:2008 Symbols for use in the labelling of medical devices