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UNE-EN 13544-2:2003

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

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withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

Respiratory therapy equipment - Part 2: Tubing and connectors.

Available format(s)

Hardcopy , PDF

Withdrawn date

22-03-2010

Language(s)

Spanish, Castilian

Published date

30-04-2003

PROLOGO
1 OBJETO Y CAMPO DE APLICACION
2 NORMAS PARA CONSULTA
3 CONECTORES NO ROSCADOS
4 CONECTORES ROSCADOS QUE SOPORTAN PESO
5 TUBOS
6 MARCADO DEL TUBO, ETIQUETAS Y ENVASE
7 ENVASE
8 APTITUD DE USO
9 EVALUACION CLINICA
ANEXO A (Normativo) - MÉTODOS DE ENSAYO
ANEXO B (Normativo) - CONECTORES ROSCADOS QUE SOPORTAN PESO
        PARA OXIGENO Y AIRE
ANEXO C (Informativo) - INFORMACION SOBRE EL MÉTODO DE ENSAYO
        DE LA SEGURIDAD DE LAS CONEXIONES
ANEXO ZA (Informativo) - CAPITULOS DE ESTA NORMA EUROPEA
         RELACIONADOS CON LOS REQUISITOS ESENCIALES U OTRAS
         DISPOSICIONES DE LA DIRECTIVA 93/42/CEE
BIBLIOGRAFIA

Describes requirements for tubing to be used with equipment for the therapeutic administration of respirable gases in domiciliary, ambulance and hospital practice including the interface to the equipment.

Committee
CTN 110
DevelopmentNote
2003 Edition Re-Issued in March 2010 & incorporates AMD 1 2010. (03/2010)
DocumentType
Standard
Pages
22
ProductNote
THIS STANDARD IS IDENTICAL TO EN 13544-2:2002
PublisherName
Asociacion Espanola de Normalizacion
Status
Withdrawn
SupersededBy

EN 13220 : 1998 FLOW-METERING DEVICES FOR CONNECTION TO TERMINAL UNITS OF MEDICAL GAS PIPELINE SYSTEMS
EN 738-1:1997/A1:2002 PRESSURE REGULATORS FOR USE WITH MEDICAL GASES - PRESSURE REGULATORS AND PRESSURE REGULATORS WITH FLOW METERING DEVICES
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)
EN 1041:2008+A1:2013 Information supplied by the manufacturer of medical devices
EN 62366 : 2008 AMD 1 2015 MEDICAL DEVICES - APPLICATION OF USABILITY ENGINEERING TO MEDICAL DEVICES (IEC 62366:2007/A1:2014)
EN ISO 10651-4:2009 Lung ventilators - Part 4: Particular requirements for operator-powered resuscitators (ISO 10651-4:2002)
EN 980:2008 Symbols for use in the labelling of medical devices

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