EN 556:1994 + A1:1998
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STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR TERMINALLY-STERILIZED MEDICAL DEVICES TO BE LABELLED "STERILE" |
EN 550 : 1994
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STERILIZATION OF MEDICAL DEVICES - VALIDATION AND ROUTINE CONTROL OF ETHYLENE OXIDE STERILIZATION |
ISO 8835-3:2007
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Inhalational anaesthesia systems Part 3: Transfer and receiving systems of active anaesthetic gas scavenging systems |
ISO 11138-3:2017
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Sterilization of health care products — Biological indicators — Part 3: Biological indicators for moist heat sterilization processes |
ISO 9703-1:1992
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Anaesthesia and respiratory care alarm signals Part 1: Visual alarm signals |
IEC 60416:1988
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General principles for the formulation of graphical symbols |
IEC 60417-1:2002
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Graphical symbols for use on equipment - Part 1: Overview and application |
ISO 11135:2014
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Sterilization of health-care products Ethylene oxide Requirements for the development, validation and routine control of a sterilization process for medical devices |
ISO 10651-2:2004
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Lung ventilators for medical use Particular requirements for basic safety and essential performance Part 2: Home care ventilators for ventilator-dependent patients |
IEC 60601-1:2005+AMD1:2012 CSV
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Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
ISO 7767:1997
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Oxygen monitors for monitoring patient breathing mixtures — Safety requirements |
ISO 5356-1:2015
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Anaesthetic and respiratory equipment Conical connectors Part 1: Cones and sockets |
ISO 9703-3:1998
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Anaesthesia and respiratory care alarm signals Part 3: Guidance on application of alarms |
NFPA 53 : 2016
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MATERIALS, EQUIPMENT, AND SYSTEMS USED IN OXYGEN-ENRICHED ATMOSPHERES |
EN 60601-1-1:2001
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Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems |
ISO 9918:1993
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Capnometers for use with humans Requirements |
ISO 5356-2:2012
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Anaesthetic and respiratory equipment — Conical connectors — Part 2: Screw-threaded weight-bearing connectors |
ISO 11138-2:2017
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Sterilization of health care products — Biological indicators — Part 2: Biological indicators for ethylene oxide sterilization processes |
ISO 5367:2014
|
Anaesthetic and respiratory equipment — Breathing sets and connectors |
IEC 60601-1-2:2014
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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
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Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests |
ISO 5359:2014
|
Anaesthetic and respiratory equipment Low-pressure hose assemblies for use with medical gases |
ISO 5362:2006
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Anaesthetic reservoir bags |
EN 1041:2008+A1:2013
|
Information supplied by the manufacturer of medical devices |
ISO 10651-3:1997
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Lung ventilators for medical use Part 3: Particular requirements for emergency and transport ventilators |
ISO 8185:2007
|
Respiratory tract humidifiers for medical use Particular requirements for respiratory humidification systems |
ISO 7396:1987
|
Non-flammable medical gas pipeline systems |
IEC 60601-2-13:2003+AMD1:2006 CSV
|
Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems |
IEC TR 60878:2015
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Graphical symbols for electrical equipment in medical practice |
EN 552:1994/A2:2000
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STERILIZATION OF MEDICAL DEVICES - VALIDATION AND ROUTINE CONTROL OF STERILIZATION BY IRRADIATION |
IEC 60417-2:1998
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Graphical symbols for use on equipment - Part 2: Symbol originals |
ISO 9919:2005
|
Medical electrical equipment Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use |
IEEE DRAFT 1073 : D3.6 SEP 95
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STANDARD FOR MEDICAL DEVICE COMMUNICATIONS OVERVIEW AND FRAMEWORK |
ISO 9360-1:2000
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Anaesthetic and respiratory equipment — Heat and moisture exchangers (HMEs) for humidifying respired gases in humans — Part 1: HMEs for use with minimum tidal volumes of 250 ml |
ISO 11138-1:2017
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Sterilization of health care products — Biological indicators — Part 1: General requirements |
ISO 11134:1994
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Sterilization of health care products — Requirements for validation and routine control — Industrial moist heat sterilization |
ISO 14971:2007
|
Medical devices Application of risk management to medical devices |
EN 60601-1-4:1996/A1:1999
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MEDICAL ELECTRICAL EQUIPMENT - GENERAL REQUIREMENTS FOR SAFETY - COLLATERAL STANDARD: PROGRAMMABLE ELECTRICAL MEDICAL SYSTEMS |
ISO 7000:2014
|
Graphical symbols for use on equipment Registered symbols |
ISO 4135:2001
|
Anaesthetic and respiratory equipment Vocabulary |
ISO 9360-2:2001
|
Anaesthetic and respiratory equipment — Heat and moisture exchangers (HMEs) for humidifying respired gases in humans — Part 2: HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml |
ISO 11137:1995
|
Sterilization of health care products Requirements for validation and routine control Radiation sterilization |
ISO 11195:1995
|
Gas mixers for medical use Stand-alone gas mixers |
IEC 60601-1-1:2000
|
Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems |
ISO 594-1:1986
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Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment Part 1: General requirements |
IEC 60601-1-4:1996+AMD1:1999 CSV
|
Medical electrical equipment - Part 1-4: General requirements for safety - Collateral Standard: Programmable electrical medical systems |
ISO 9703-2:1994
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Anaesthesia and respiratory care alarm signals — Part 2: Auditory alarm signals |
EN 554 : 1994
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STERILIZATION OF MEDICAL DEVICES - VALIDATION AND ROUTINE CONTROL OF STERILIZATION BY MOIST HEAT |
ISO 15223:2000
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Medical devices Symbols to be used with medical device labels, labelling and information to be supplied |