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ISO/IEC TR 10000-1:1998
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Information technology Framework and taxonomy of International Standardized Profiles Part 1: General principles and documentation framework |
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EN 556:1994 + A1:1998
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STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR TERMINALLY-STERILIZED MEDICAL DEVICES TO BE LABELLED "STERILE" |
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ISO 10241:1992
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International terminology standards Preparation and layout |
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EN 550 : 1994
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STERILIZATION OF MEDICAL DEVICES - VALIDATION AND ROUTINE CONTROL OF ETHYLENE OXIDE STERILIZATION |
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ISO 690:2010
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Information and documentation Guidelines for bibliographic references and citations to information resources |
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ISO 11138-3:2017
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Sterilization of health care products — Biological indicators — Part 3: Biological indicators for moist heat sterilization processes |
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ISO 9703-1:1992
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Anaesthesia and respiratory care alarm signals Part 1: Visual alarm signals |
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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 |
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IEC 60601-1:2005+AMD1:2012 CSV
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Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
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IEC 60601-1-6:2010+AMD1:2013 CSV
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Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability |
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ISO 7767:1997
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Oxygen monitors for monitoring patient breathing mixtures — Safety requirements |
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ISO 5356-1:2015
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Anaesthetic and respiratory equipment Conical connectors Part 1: Cones and sockets |
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ISO 9703-3:1998
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Anaesthesia and respiratory care alarm signals Part 3: Guidance on application of alarms |
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NFPA 53 : 2016
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MATERIALS, EQUIPMENT, AND SYSTEMS USED IN OXYGEN-ENRICHED ATMOSPHERES |
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ISO 9918:1993
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Capnometers for use with humans Requirements |
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IEC TR 60513:1994
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Fundamental aspects of safety standards for medical electrical equipment |
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ISO 5356-2:2012
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Anaesthetic and respiratory equipment — Conical connectors — Part 2: Screw-threaded weight-bearing connectors |
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ISO 11138-2:2017
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Sterilization of health care products — Biological indicators — Part 2: Biological indicators for ethylene oxide sterilization processes |
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ISO 32:1977
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Gas cylinders for medical use — Marking for identification of content |
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ISO 5367:2014
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Anaesthetic and respiratory equipment — Breathing sets and connectors |
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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 |
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ISO 5359:2014
|
Anaesthetic and respiratory equipment Low-pressure hose assemblies for use with medical gases |
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ISO 5362:2006
|
Anaesthetic reservoir bags |
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EN 1041:2008+A1:2013
|
Information supplied by the manufacturer of medical devices |
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ISO 8185:2007
|
Respiratory tract humidifiers for medical use Particular requirements for respiratory humidification systems |
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ISO/TR 16142:2006
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Medical devices Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices |
|
ISO 23328-2:2002
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Breathing system filters for anaesthetic and respiratory use — Part 2: Non-filtration aspects |
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EN 552:1994/A2:2000
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STERILIZATION OF MEDICAL DEVICES - VALIDATION AND ROUTINE CONTROL OF STERILIZATION BY IRRADIATION |
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IEC 80416-1:2008
|
Basic principles for graphical symbols for use on equipment - Part 1: Creation of graphical symbols for registration |
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ISO 9919:2005
|
Medical electrical equipment Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use |
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ISO 9360-1:2000
|
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
|
Sterilization of health care products — Biological indicators — Part 1: General requirements |
|
ISO 11134:1994
|
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 |
|
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 |
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EN 13014:2000/AC:2002
|
CONNECTIONS FOR GAS SAMPLING TUBES TO ANAESTHETIC AND RESPIRATORY EQUIPMENT |
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ISO 11137:1995
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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 |
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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
|
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 |
|
EN 554 : 1994
|
STERILIZATION OF MEDICAL DEVICES - VALIDATION AND ROUTINE CONTROL OF STERILIZATION BY MOIST HEAT |
|
ISO 15223:2000
|
Medical devices Symbols to be used with medical device labels, labelling and information to be supplied |
|
ISO 7396-1:2016
|
Medical gas pipeline systems — Part 1: Pipeline systems for compressed medical gases and vacuum |