UNE-EN 13544-1:2007

Withdrawn

View Superseded by

Respiratory therapy equipment - Part 1: Nebulizing systems and their components

Available format(s)

Hardcopy , PDF

Withdrawn date

03-22-2010

Language(s)

Spanish, Castilian, English

Published date

10-24-2007

Publisher

Asociacion Espanola de Normalizacion

Committee	CTN 110
DevelopmentNote	2007 Edition Re-Issued in March 2010 & incorporates AMD 1 2010. (03/2010)
DocumentType	Standard
Pages	42
PublisherName	Asociacion Espanola de Normalizacion
Status	Withdrawn
SupersededBy	UNE-EN 13544-1:2007+A1:2010
Supersedes	UNE-EN 13544-1:2002 UNE-EN 13544-1/A1:2004

Standards	Relationship
DIN EN 13544-1:2009-12	Identical
NS EN 13544-1 : 2007 + A1 2009	Identical
UNI EN 13544-1 : 2009	Identical
NBN EN 13544-1 : 2007 + A1 2009	Identical
EN 13544-1:2007	Identical
BS EN 13544-1 : 2007	Identical
I.S. EN 13544-1:2007	Identical
EN 13544-1:2007+A1:2009	Identical
SN EN 13544-1 : 2007 + A1 2010	Identical
NF EN 13544-1 : 2007 + A1 2009	Identical
NEN EN 13544-1 : 2007 + A1 2009	Identical

IEC 61672-2:2013+AMD1:2017 CSV	Electroacoustics - Sound level meters - Part 2: Pattern evaluation tests
ISO 11137-1:2006	Sterilization of health care products Radiation Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
EN 556:1994 + A1:1998	STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR TERMINALLY-STERILIZED MEDICAL DEVICES TO BE LABELLED "STERILE"
ISO 3744:2010	Acoustics Determination of sound power levels and sound energy levels of noise sources using sound pressure Engineering methods for an essentially free field over a reflecting plane
ENV 737-6 : DRAFT 2003	MEDICAL GAS PIPELINE SYSTEMS - PART 6: DIMENSIONS AND ALLOCATION OF PROBES FOR TERMINAL UNITS FOR COMPRESSED MEDICAL GASES AND VACUUM
ISO 9276-1:1998	Representation of results of particle size analysis — Part 1: Graphical representation
EN ISO 10524-3:2006/A1:2013	PRESSURE REGULATORS FOR USE WITH MEDICAL GASES - PART 3: PRESSURE REGULATORS INTEGRATED WITH CYLINDER VALVES (ISO 10524-3:2005/AMD 1:2013)
EN ISO 5356-1:2015	Anaesthetic and respiratory equipment - Conical connectors - Part 1: Cones and sockets (ISO 5356-1:2015)
EN 61672-2:2013/A1:2017	ELECTROACOUSTICS - SOUND LEVEL METERS - PART 2: PATTERN EVALUATION TESTS (IEC 61672-2:2013/A1:2017)
IEC 60601-1:2005+AMD1:2012 CSV	Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
ISO 15001:2010	Anaesthetic and respiratory equipment Compatibility with oxygen
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
ISO 5356-1:2015	Anaesthetic and respiratory equipment Conical connectors Part 1: Cones and sockets
EN 737-1 : 1998	MEDICAL GAS PIPELINE SYSTEMS - TERMINAL UNITS FOR COMPRESSED MEDICAL GASES AND VACUUM
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 61000-4-2:2009	Electromagnetic compatibility (EMC) - Part 4-2: Testing and measurement techniques - Electrostatic discharge immunity test
EN 1281-2 : 1995	ANAESTHETIC AND RESPIRATORY EQUIPMENT - CONICAL CONNECTORS - SCREW-THREADED WEIGHT-BEARING CONNECTORS
EN 62304:2006/A1:2015	MEDICAL DEVICE SOFTWARE - SOFTWARE LIFE-CYCLE PROCESSES (IEC 62304:2006/A1:2015)
ISO 5356-2:2012	Anaesthetic and respiratory equipment — Conical connectors — Part 2: Screw-threaded weight-bearing connectors
IEC 62366:2007+AMD1:2014 CSV	Medical devices - Application of usability engineering to medical devices
ISO 11135-1:2007	Sterilization of health care products Ethylene oxide Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
IEC 60601-1-2:2014	Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
EN 60601-1-2:2015	Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
EN 1041:2008+A1:2013	Information supplied by the manufacturer of medical devices
ISO 8185:2007	Respiratory tract humidifiers for medical use Particular requirements for respiratory humidification systems
ISO 10524-3:2005	Pressure regulators for use with medical gases Part 3: Pressure regulators integrated with cylinder valves
IEC 62304:2006+AMD1:2015 CSV	Medical device software - Software life cycle processes
EN 739:1998/A1:2002	LOW-PRESSURE HOSE ASSEMBLIES FOR USE WITH MEDICAL GASES
EN ISO 11137-2:2015	Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013)
EN 61672-1:2013	Electroacoustics - Sound level meters - Part 1: Specifications
ISO 11137-3:2017	Sterilization of health care products — Radiation — Part 3: Guidance on dosimetric aspects of development, validation and routine control
EN ISO 3744:2010	Acoustics - Determination of sound power levels and sound energy levels of noise sources using sound pressure - Engineering methods for an essentially free field over a reflecting plane (ISO 3744:2010)
EN ISO 15001:2011	Anaesthetic and respiratory equipment - Compatibility with oxygen (ISO 15001:2010)
EN ISO 11135-1:2007	Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007)
IEC 61000-4-2:2008	Electromagnetic compatibility (EMC) - Part 4-2: Testing and measurement techniques - Electrostatic discharge immunity test
ISO 11137-2:2013	Sterilization of health care products — Radiation — Part 2: Establishing the sterilization dose
EN ISO 7396-1:2016	Medical gas pipeline systems - Part 1: Pipeline systems for compressed medical gases and vacuum (ISO 7396-1:2016)
EN 62366 : 2008 AMD 1 2015	MEDICAL DEVICES - APPLICATION OF USABILITY ENGINEERING TO MEDICAL DEVICES (IEC 62366:2007/A1:2014)
NFPA 53M : 1990	FIRE HAZARDS IN OXYGEN-ENRICHED ATMOSPHERES
EN ISO 11137-1:2015	Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd 1:2013)
EN ISO 14971:2012	Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
EN ISO 17665-1 : 2006	Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006)
ISO 14971:2007	Medical devices Application of risk management to medical devices
ISO 4135:2001	Anaesthetic and respiratory equipment Vocabulary
EN ISO 10524-1:2006	Pressure regulators for use with medical gases - Part 1: Pressure regulators and pressure regulators with flow-metering devices (ISO 10524-1:2006)
EN ISO 4135:2001	ANAESTHETIC AND RESPIRATORY EQUIPMENT - VOCABULARY
ISO 10524-1:2006	Pressure regulators for use with medical gases Part 1: Pressure regulators and pressure regulators with flow-metering devices
EN ISO 8185:2009	Respiratory tract humidifiers for medical use - Particular requirements for respiratory humidification systems (ISO 8185:2007)
EN 20594-1:1993/A1:1997	CONICAL FITTINGS WITH A 6% (LUER) TAPER FOR SYRINGES, NEEDLES AND CERTAIN OTHER MEDICAL EQUIPMENT - GENERAL REQUIREMENTS
EN 980:2008	Symbols for use in the labelling of medical devices
EN 1707 : 1996	CONICAL FITTINGS WITH A 6 % (LUER) TAPER FOR SYRINGES, NEEDLES AND CERTAIN OTHER MEDICAL EQUIPMENT - LOCK FITTINGS
ISO 594-1:1986	Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment Part 1: General requirements
EN ISO 11137-3:2017	Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control (ISO 11137-3:2017)
ISO 9276-2:2014	Representation of results of particle size analysis Part 2: Calculation of average particle sizes/diameters and moments from particle size distributions
ISO 17665-1:2006	Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
ISO 7396-1:2016	Medical gas pipeline systems — Part 1: Pipeline systems for compressed medical gases and vacuum