UNE-EN 1782:1998
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
TRACHEAL TUBES AND CONNECTORS.
Hardcopy , PDF
Spanish, Castilian
05-11-1998
01-11-2015
PROLOGO
INTRODUCCION
1 OBJETO Y CAMPO DE APLICACION
2 NORMAS PARA CONSULTA
3 DEFINICIONES
4 REQUISITOS GENERALES PARA LOS TUBOS TRAQUEALES
Y LOS CONECTORES DE TUBOS TRAQUEALES
5 REQUISITOS ADICIONALES PARA TUBOS TRAQUEALES CON UNA
FENESTRACION DE MURPHY
6 REQUISITOS PARA LOS TUBOS TRAQUEALES Y LOS
CONECTORES DE TUBOS TRAQUEALES SUMINISTRADOS ESTÉRILES
7 MARCADO
ANEXO A (Normativo) - MÉTODO DEL ENSAYO PARA DETERMINAR
EL DIAMETRO DEL MANGUITO EN REPOSO
ANEXO B (Normativo) - MÉTODO DEL ENSAYO PARA DETERMINAR
LA RESISTENCIA DEL TUBO AL APLASTAMIENTO
ANEXO C (Normativo) - MÉTODO DEL ENSAYO PARA DETERMINAR
EL HERNIADO DEL MANGUITO
ANEXO D (Informativo) - RECOMENDACIONES SOBRE LOS
MATERIALES Y EL DISENO
ANEXO E (Informativo) - BIBLIOGRAFIA
ANEXO ZA (Informativo) - CAPITULOS DE ESTA NORMA EUROPEA
RELACIONADOS CON LOS REQUISITOS ESENCIALES U
OTRAS DISPOSICIONES DE LA DIRECTIVA 93/42/CEE
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. Does not include specialized tubes.
| Committee |
CTN 110
|
| DevelopmentNote |
Supersedes UNE 110007-1 & UNE 110007-2. (03/2010) 1998 Edition Re-Issued in March 2010 & incorporates AMD 1 2010. (03/2010)
|
| DocumentType |
Standard
|
| Pages |
34
|
| PublisherName |
Asociación Española de Normalización
|
| Status |
Superseded
|
| Standards | Relationship |
| I.S. EN 1782:1998 | Identical |
| NEN EN 1782 : 1998 + A1 2009 | Identical |
| NF EN 1782 : 1998 + A1 2009 | Identical |
| EN 1782:1998+A1:2009 | Identical |
| DIN EN 1782:2009-12 | Identical |
| NS EN 1782 : 1998 + A1 2009 | Identical |
| BS EN 1782 : 1998 | Identical |
| NBN EN 1782 : 1998 + A1 2009 | 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 |
| 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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