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medical access

medical access, Total:363 items.

In the international standard classification, medical access involves: Medical equipment, Applications of information technology, Medical sciences and health care facilities in general, Sterilization and disinfection, Vocabularies, First aid, Special purpose vehicles, Pharmaceutics, Graphical symbols, Telecommunication systems, Aids for disabled or handicapped persons, Services, Paper products, Aircraft and space vehicles in general, Transport, Laboratory medicine, Character sets and information coding, Veterinary medicine, Accident and disaster control, Ventilators. Fans. Air-conditioners, Networking, Photography, Machine tools, Measurement of time, velocity, acceleration, angular velocity, CONSTRUCTION MATERIALS AND BUILDING, HEALTH CARE TECHNOLOGY, Hospital equipment, Dentistry, Home textiles. Linen.


International Organization for Standardization (ISO), medical access

  • ISO/DIS 18562-2 Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 2: Tests for emissions of particulate matter
  • ISO/DIS 18562-3 Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 3: Tests for emissions of volatile organic substances
  • ISO/DIS 18562-4 Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 4: Tests for leachables in condensate
  • ISO/FDIS 18562-4:2014 Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 4: Tests for leachables in condensate
  • ISO/FDIS 18562-3:2014 Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 3: Tests for emissions of volatile organic substances
  • ISO/IEEE 11073-20702:2018 Health informatics — Point-of-care medical device communication — Part 20702: Medical devices communication profile for web services
  • ISO/DIS 18562-1 Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 1: Evaluation and testing within a risk management process
  • ISO 7396-1:2007/Amd 1:2010 Medical gas pipeline systems - Part 1: Pipeline systems for compressed medical gases and vacuum - Amendment 1: Requirements for terminal units for vacuum fitted on medical supply units with operator-adjustable portions and connected to the pipeline throug
  • ISO 15223-1:2016 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements
  • ISO 15223-1:2012 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements
  • IEC TR 80001-2-4:2012 Application of risk management for IT-networks incorporating medical devices — Part 2-4: General implementation guidance for Healthcare Delivery Organizations
  • ISO 18250-1:2018 Medical devices — Connectors for reservoir delivery systems for healthcare applications — Part 1: General requirements and common test methods
  • ISO 13408-1:1998 Aseptic processing of health care products - Part 1: General requirements
  • ISO 11138-1:1994 Sterilization of health care products - Biological indicators - Part 1: General
  • ISO 11140-1:1995 Sterilization of health care products - Chemical indicators - Part 1: General requirements
  • ISO 16142-1:2016 Medical devices - Recognized essential principles of safety and performance of medical devices - Part 1: General essential principles and additional specific essential principles for all non-IVD medical devices and guidance on the selection of standards
  • IEC TR 80001-2-2:2012 Application of risk management for IT-networks incorporating medical devices — Part 2-2: Guidance for the communication of medical device security needs, risks and controls
  • IEC/TR 80001-2-2:2012 Application of risk management for IT-networks incorporating medical devices — Part 2-2: Guidance for the communication of medical device security needs, risks and controls
  • ISO 11138-1:2017 Sterilization of health care products - Biological indicators - Part 1: General requirements
  • ISO/CD TS 9321:2023 Health informatics — General requirements of multi-center medical data collaborative analysis
  • IEC TR 80001-2-2:2012 Application of risk management for IT-networks incorporating medical devices — Part 2-2: Guidance for the communication of medical device security needs, risks and controls
  • ISO/IEEE 11073-20701:2020 Health informatics — Device interoperability — Part 20701: Point-of-care medical device communication — Service oriented medical device exchange architecture and protocol binding
  • ISO/IEEE 11073-10101:2004 Health informatics - Point-of-care medical device communication - Part 10101: Nomenclature
  • ISO 8600-1:2015 Endoscopes - Medical endoscopes and endotherapy devices - Part 1: General requirements
  • ISO 8600-1:2013 Endoscopes - Medical endoscopes and endotherapy devices - Part 1: General requirements
  • ISO 13606-5:2010 Health informatics - Electronic health record communication - Part 5: Interface specification
  • ISO 11140-1:1995/Amd 1:1998 Sterilization of health care products - Chemical indicators - Part 1: General requirements; Amendment 1
  • ISO 5258:2022 Healthcare organization management — Pandemic response (respiratory) — Drive-through screening station
  • IEC TR 80001-2-2:2012 Application of risk management for IT-networks incorporating medical devices — Part 2-2: Guidance for the communication of medical device security needs, risks and controls
  • ISO 80601-2-72:2015 Medical electrical equipment - Part 2-72: Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients

国家药监局, medical access

  • YY/T 1778.1-2021 Biocompatibility evaluation of respiratory gas pathways in medical applications Part 1: Evaluation and testing during risk management
  • YY/T 1754.1-2020 Preclinical Animal Studies for Medical Devices Part 1: General Requirements

Association Francaise de Normalisation, medical access

  • NF S95-189-2*NF EN ISO 18562-2:2020 Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 2 : tests for emissions of particulate matter
  • NF S95-189-4*NF EN ISO 18562-4:2020 Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 4 : tests for leachables in condensate
  • NF EN ISO 18562-4:2020 Évaluation de la biocompatibilité des voies de gaz respiratoires dans les applications de soins de santé - Partie 4 : essais concernant les substances relargables dans le condensat
  • NF S95-189-3*NF EN ISO 18562-3:2020 Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 3 : tests for emissions of volatile organic compounds (VOCs)
  • NF S95-189-1*NF EN ISO 18562-1:2020 Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 1 : evaluation and testing within a risk management process
  • NF EN ISO 18562-3:2020 Évaluation de la biocompatibilité des voies de gaz respiratoires dans les applications de soins de santé - Partie 3 : essais concernant les émissions de composés organiques volatils (COV)
  • XP S98-224*XP ISO/TS 22421:2021 Sterilization of health care products - Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
  • XP ISO/TS 22421:2021 Stérilisation des produits de santé - Exigences communes applicables aux stérilisateurs utilisés pour la stérilisation terminale des dispositifs médicaux dans les établissements de santé
  • NF S64-021:2007 Medical vehicles and their equipment - Road ambulances.
  • NF S64-021*NF EN 1789:2021 Medical vehicles and their equipment - Road ambulances
  • NF EN 1789:2021 Véhicules de transport sanitaire et leurs équipements - Ambulances routières
  • NF EN 1789/IN2:2014 Véhicules de transport sanitaire et leurs équipements - Ambulances routières
  • NF EN 13532:2002 Exigences générales relatives aux dispositifs médicaux de diagnostic in vitro pour auto-test
  • NF S99-014-1:2012 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1 : general requirements.
  • NF S95-202-1:2008 Medical vehicles and their equipment - Air ambulances - Part 1 : requirements for medical devices used in air ambulances.
  • NF S95-202-1:2017 Medical vehicles and their equipment - Air ambulances - Part 1 : requirements for medical devices used in air ambulances
  • NF C74-018/A1*NF EN 60601-1-8/A1:2013 Medical electrical equipment - Part 1-8 : general requirements for basic safety and essential performance - Collateral Standard : general requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
  • NF EN 60601-1-11/A1:2021 Appareils électromédicaux - Partie 1-11 : exigences générales pour la sécurité de base et les performances essentielles - Norme Collatérale : exigences pour les appareils électromédicaux et les systèmes électromédicaux utilisés dans l'env...
  • NF S97-530:2002 Medical informatics - Messages concerning blood transfusion - Communication and data model.
  • NF S97-518-10101:2006 Health informatics - Point-of-care medical device communications - Part 10101 : nomenclature.
  • NF S98-103/A2:2001 Sterilization of medical devices - Validation and routine control of sterilization by irradiation.
  • NF EN 14822-2:2007 Informatique de la santé - Composants d'information d'usage général - Partie 2 : informations non médicales

British Standards Institution (BSI), medical access

  • DD ENV 12052-1998 Medical informatics. Medical imaging communication (MEDICOM)
  • DD ENV 12623-1998 Medical informatics. Media interchange in Medical imaging communications (MI-MEDICOM)
  • BS EN 1789:2007 Medical vehicles and their equipment - Road ambulances
  • BS EN 1789:2007+A1:2010 Medical vehicles and their equipment - Road ambulances
  • BS EN 1789:2020 Medical vehicles and their equipment. Road ambulances
  • BS ISO/IEEE 11073-20702:2018 Health informatics. Point-of-care medical device communication. Medical devices communication profile for web services
  • PD ISO/TS 22421:2021 Sterilization of health care products. Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
  • PD ISO/TS 21560:2020 General requirements of tissue-engineered medical products
  • BS EN ISO 15223-1:2017 Medical devices. Symbols to be used with medical device labels, labelling and information to be supplied. General requirements
  • BS EN ISO 15223-1:2012 Medical devices. Symbols to be used with medical device labels, labelling and information to be supplied. General requirements
  • BS PD IEC/TR 62354:2014 General testing procedures for medical electrical equipment
  • BS EN 60601-1-12:2015 Medical electrical equipment. General requirements for basic safety and essential performance. Collateral Standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment
  • 18/30383808 DC BS EN 1789. Medical vehicles and their equipment. Road ambulances
  • 23/30464861 DC BS EN 1789 AMD1. Medical vehicles and their equipment. Road ambulances
  • BS EN ISO 11073-10101:2006 Health informatics - Point-of-care medical device communications - Nomenclature
  • BS ISO 8600-1:2013 Endoscopes. Medical endoscopes and endotherapy devices. General requirements
  • BS DD ENV 13608-3:2000 Health informatics - Security for healthcare communication - Secure data channels
  • DD ENV 13608-3:2000 Health informatics. Security for healthcare communication. Secure data channels
  • BS EN 60601-1-8:2007+A1:2013 Medical electrical equipment. General requirements for basic safety and essential performance. Collateral Standard. General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
  • BS EN ISO 11073-20701:2020 Health informatics. Device interoperability - Point-of-care medical device communication. Service oriented medical device exchange architecture and protocol binding
  • BS DD ENV 13608-1:2000 Health informatics - Security for healthcare communication - Concepts and terminology
  • BS ISO 17432:2005 Health informatics - Messages and communication - Web access to DICOM persistent objects
  • DD ENV 13608-1:2000 Health informatics. Security for healthcare communication. Concepts and terminology
  • BS DD ENV 13608-2:2000 Health informatics - Security for healthcare communication - Secure data objects
  • DD ENV 13608-2:2000 Health informatics. Security for healthcare communication. Secure data objects
  • BS EN 60601-1-8:2007 Medical electrical equipment. General requirements for basic safety and essential performance. Collateral Standard. General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
  • PD ISO/TR 21730:2007 Health informatics. Use of mobile wireless communication and computing technology in healthcare facilities. Recommendations for electromagnetic compatibility (management of unintentional electromagnetic interference) with medical devices
  • BS EN ISO 11073-30200:2006 Health informatics - Point-of-care medical device communication - Transport profile - Cable connected
  • BS EN ISO 11073-30300:2005 Health informatics. Point-of-care medical device communication. Transport profile. Infrared wireless
  • BS EN ISO 11073-10101:2020 Health informatics. Device interoperability - Point-of-care medical device communication. Nomenclature

German Institute for Standardization, medical access

  • DIN EN ISO 18562-4:2020-05 Biocompatibility evaluation of breathing gas pathways in healthcare application - Part 4: Tests for leachables in condensate (ISO 18562-4:2017); German version EN ISO 18562-4:2020 / Note: To be replaced by DIN EN ISO 18562-4 (2022-12).
  • DIN EN ISO 18562-2:2020 Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 2: Tests for emissions of particulate matter (ISO 18562-2:2017)
  • DIN EN ISO 18562-4:2020 Biocompatibility evaluation of breathing gas pathways in healthcare application - Part 4: Tests for leachables in condensate (ISO 18562-4:2017)
  • DIN EN ISO 18562-1:2020 Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 1: Evaluation and testing within a risk management process (ISO 18562-1:2017)
  • DIN EN ISO 18562-3:2020 Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 3: Tests for emissions of volatile organic compounds (VOCs) (ISO 18562-3:2017)
  • DIN EN 1789:2007 Medical vehicles and their equipment - Road ambulances; German version EN 1789:2007
  • DIN EN 1789 Berichtigung 1:2021-08 Medical vehicles and their equipment - Road ambulances; German version EN 1789:2020; Corrigendum 1
  • DIN EN 1789/A1:2023-01 Medical vehicles and their equipment - Road ambulances; German and English version EN 1789:2020/prA1:2023 / Note: Date of issue 2022-12-09*Intended as an amendment to DIN EN 1789 (2020-12).
  • DIN EN 1789:2020-12 Medical vehicles and their equipment - Road ambulances; German version EN 1789:2020 / Note: To be amended by DIN EN 1789/A1 (2023-01).
  • DIN EN 60601-1-11 Berichtigung 1:2011 Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment (IEC 6060
  • DIN EN 13532:2002-08 General requirements for in vitro diagnostic medical devices for self-testing; German version EN 13532:2002, German and English texts
  • DIN EN 13718-1:2008 Medical vehicles and their equipment - Air ambulances - Part 1: Requirements for medical devices used in air ambulances; English version of DIN EN 13718-1:2008-11
  • DIN EN 13718-1:2014 Medical vehicles and their equipment - Air ambulances - Part 1: Requirements for medical devices used in air ambulances; German version EN 13718-1:2014
  • DIN EN 1789:2020 Medical vehicles and their equipment - Road ambulances; German version EN 1789:2020
  • DIN 1946-4:2018-09 Ventilation and air conditioning - Part 4: Ventilation in buildings and rooms of health care
  • DIN EN 60601-1-12:2016 Medical electrical equipment - Part 1-12: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical service
  • DIN EN 1789:2014 Medical vehicles and their equipment - Road ambulances; German version EN 1789:2007+A2:2014
  • DIN EN 1789:2010 Medical vehicles and their equipment - Road ambulances; German version EN 1789:2007+A1:2010
  • DIN EN ISO 21549-2:2014 Health informatics - Patient healthcard data - Part 2: Common objects (ISO 21549-2:2014); English version EN ISO 21549-2:2014
  • DIN EN ISO 11073-20701:2020-07 Health informatics - Device interoperability - Part 20701: Point-of-care medical device communication - Service-oriented medical device exchange architecture and protocol binding (ISO/IEEE 11073-20701:2020); English version EN ISO 11073-20701:2020
  • DIN 6878-1:2013 Digital archiving in medical radiology.Part 1: General requirements for the archiving of images
  • DIN V ENV 13606-4:2000-09 Health informatics - Electronic healthcare record communication - Part 4: Messages for the exchange of information; English version ENV 13606-4:2000 / Note: To be replaced by DIN EN 13606-4 (2006-05), DIN EN ISO 13606-5 (2008-06).

European Committee for Standardization (CEN), medical access

  • prEN ISO 18562-2 Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 2: Tests for emissions of particulate matter (ISO/DIS 18562-2:2022)
  • prEN ISO 18562-3 Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 3: Tests for emissions of volatile organic substances (ISO/DIS 18562-3:2022)
  • prEN ISO 18562-4 Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 4: Tests for leachables in condensate (ISO/DIS 18562-4:2022)
  • prEN ISO 18562-1 Biocompatibility evaluation of breathing gas pathways in healthcare applications - Part 1: Evaluation and testing within a risk management process (ISO/DIS 18562-1:2022)
  • EN 1789:2007+A2:2014 Medical vehicles and their equipment - Road ambulances
  • EN ISO 15223-1:2021 Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021)
  • EN ISO 15223-1:2012 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (Remains Current)
  • DD ENV 12539-1997 Medical Informatics - Request and Report Messages for Diagnostic Service Departments
  • EN ISO 13606-5:2019 Health informatics - Electronic health record communication - Part 5: Interface specification (ISO 13606-5:2019)
  • EN ISO 13606-5:2010 Health informatics - Electronic health record communication - Part 5: Interface specification
  • DD ENV 13606-1-2000 Health Informatics - Electronic Healthcare Record Communication - Part 1: Extended Architecture
  • DD ENV 13606-2-2000 Health Informatics - Electronic Healthcare Record Communication - Part 2: Domain Term List
  • EN ISO 11073-10201:2005 Health informatics - Point-of-care medical device communication - Part 10201: Domain information model (ISO/IEEE 11073-10201:2004)
  • DD ENV 13606-4-2000 Health Informatics - Electronic Healthcare Record Communication - Part 4: Messages for the Exchange of Information

国家卫生计生委, medical access

  • WS/T 527-2016 Naming of general medical service locations within medical institutions
  • WS/T 546-2017 Interaction specifications between telemedicine information system and unified communications platform

IEEE - The Institute of Electrical and Electronics Engineers@ Inc., medical access

  • IEEE 11073-10207-2017 Health informatics - Point-of-care medical device communication - Part 10207: Domain Information and Service Model for Service-Oriented Point-of-Care Medical Device Communication
  • IEEE P11073-10101/D8-2019 Standard for Health Informatics—Point-of-Care Medical Device Communication—Nomenclature
  • IEEE 11073-20702-2018 Health informatics - Point-of-care medical device communication - Part 20702: Medical Devices Communication Profile for Web Services
  • IEEE 11073-20702-2016 Health informatics-Point-of-care medical device communication Part 20702: Medical Devices Communication Profile for Web Services
  • IEEE 1073-1996 Standard for Medical Device Communications Overview and Framework
  • IEEE 11073-10207-2019 Health informatics - Personal health device communication - Part 10207: Domain information and service model for service-oriented point-ofcare medical device communication
  • IEEE 1073.4.1-1994 Standard for Medical Device Communications Physical Layer Interface - Cable Connected
  • IEEE P11073-10101/D9-2019 Standard for Health Informatics-Point-of-Care Medical Device Communication-Nomenclature
  • IEEE P11073-10101/D7-2019 Standard for Health Informatics-Point-of-Care Medical Device Communication-Nomenclature
  • IEEE P11073-10101/D5-2019 Standard for Health Informatics-Point-of-Care Medical Device Communication-Nomenclature
  • IEEE 11073-10101-2004 Health informatics - Point-of-care medical device communication - Part 10101: Nomenclature
  • IEEE P11073-20701/D4-2018 Health informatics-Point-of-care medical device communication-Part 20701: Draft Standard for Service-Oriented Medical Device Exchange Architecture and Protocol Binding
  • IEEE 1073.3.2-2000 Standard for Medical Device Communications - Transport Profile - IrDA Based - Cable Connected
  • IEEE P11073-10101/D1-2018 Draft Standard for Health Informatics-Point-of-Care Medical Device Communication-Nomenclature
  • IEEE P11073-10101/D4-2019 Draft Standard for Health Informatics-Point-of-Care Medical Device Communication-Nomenclature
  • IEEE P11073-10201/D2.1.10-2018 Health informatics - Point-of-care medical device communication - Part 10201: Domain information model
  • IEEE P11073-10201/D2.1.9-2018 Health informatics - Point-of-care medical device communication - Part 10201: Domain information model
  • IEEE 11073-10201-2018 Health informatics-Point-of-care medical device communication Part 10201: Domain Information Model

Institute of Electrical and Electronics Engineers (IEEE), medical access

  • IEEE Std 11073-10207-2017 IEEE Health informatics--Point-of-care medical device communication Part 10207: Domain Information and Service Model for Service-Oriented Point-of-Care Medical Device Communication
  • IEEE P1073.1.3.11/D3.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Capnometer
  • IEEE P1073.1.3.6/D6.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - ECG
  • IEEE P1073.1.3.7/D4.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Blood Pressure
  • IEEE P1073.1.3.8/D4.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Temperature
  • IEEE P1073.1.3.5/D04:2000 Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Defibrillator Device
  • IEEE P1073.1.3.10/D3.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Cardiac Output
  • IEEE P1073.1.3.9/D3.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Airway Flow
  • IEEE Std P1073.1.3.8/D4.0 IEEE Draft Standard for Medical Device Communications -- Medical Device Data Language (MDDL) Virtual Medical Device, Specialized -- Temperature
  • IEEE P1073.1.3.4/D3.0 IEEE Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Medical Device Specializations - Pulse Oximeter
  • IEEE Std P1073.1.3.10/D3.0-1999 IEEE Draft Standard for Medical Device Communications -- Medical Device Data Language (MDDL) Virtual Medical Device, Specialized -- Cardiac Output
  • IEEE P1073.1.3.4/D3.0:1999 (Draft)Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Pulse Oximeter
  • IEEE P11073-10101/D1, June 2018 IEEE Draft Standard for Health Informatics—Point-of-Care Medical Device Communication—Part 10101: Nomenclature
  • IEEE P11073-10201/D2.1.10 October 2018 IEEE Draft Standard for Health Informatics - Point-of-Care Medical Device Communication - Domain Information Model
  • IEEE Std 11073-20702-2016 IEEE Health informatics--Point-of-care medical device communication Part 20702: Medical Devices Communication Profile for Web Services
  • IEEE Unapproved Draft Std P11073-00101/D03, Sep 20 Health Informatics - Point-Of-Care Medical Device Communication - Technical Report - Guidelines for the Use of RF Wireless Technology
  • IEEE Std P1073.1.3.5/D0.04 Unapproved IEEE Draft Standard for Medical Device Communications -Medical Device Data Language (MDDL) Virtual Medical Device, Specialized -Cardiac Output (Withdrawn PAR)
  • IEEE Std P1073.1.3.11/D3.0 Unapproved IEEE Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized Capnometer
  • IEEE Std P1073.2.0/D0.05 Proposed Draft IEEE Standard - Medical Device Communications - Medical Device Application Profiles (MDAP) - Base Standard
  • IEEE Std P1073.1.3.9/D3.0 Unapproved IEEE Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Airway Flow (Withdrawn PAR)
  • IEEE Std P1073.1.3.7/D4.0 Unapproved IEEE Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL)Virtual Medical Device, Specialized - Pulse Oximeter (Withdrawn PAR)
  • IEEE Std 1073-1996 IEEE Standard for Medical Device Communications--Overview and Framework
  • IEEE 1073.4.1-2000 Medical device communications - Physical layer interface - Cable connected
  • IEEE Std P1073.1.2.1/D6 Unapproved IEEE Standard IEEE Draft Health Informatics - Point-Of-Care Medical Device Communications - Domain Information Model
  • IEEE/ISO 11073-20702-2018 ISO/IEEE International Standard for Health informatics -- Point-of-care medical device communication -- Part 20702: Medical devices communication profile for web services
  • ISO/IEEE 11073-20702:2018(E) ISO/IEEE International Standard for Health informatics -- Point-of-care medical device communication -- Part 20702: Medical devices communication profile for web services
  • IEEE P1073.3.3/D8, July 2003 IEEE Draft Standard for Health Informatics - Point-of-Care Medical Device Communication - Transport profile - IrDA based - Infrared Wireless
  • IEEE 1073.3.3-2004 IEEE Draft Standard for Health Informatics - Point-of-Care Medical Device Communication - Transport profile - IrDA based - Infrared Wireless
  • IEEE Std P1073.2.1.1/D08 Unapproved IEEE Draft Standard for Health Informatics - Point-Of Care Medical Device Communication - Application Profiles - Base Standard
  • IEEE 1847-2019 IEEE Recommended Practice for Common Framework of Location Services for Healthcare
  • IEEE 11073-20701-2018 Health informatics--Point-of-care medical device communication - Part 20701: Service-Oriented Medical Device Exchange Architecture and Protocol Binding
  • IEEE Std 11073-20701-2018 Health informatics--Point-of-care medical device communication - Part 20701: Service-Oriented Medical Device Exchange Architecture and Protocol Binding
  • IEEE Std 1073.4.1-1994 IEEE Standard for Medical Device Communications-Physical Layer Interface-Cable Connected
  • IEEE Std 1073.4.1-2000 IEEE Standard for Medical Device Communications - Physical Layer Interface - Cable Connected
  • IEEE Std 1073.4.1, 2000 Edition IEEE Standard for Medical Device Communications - Physical Layer Interface - Cable Connected
  • IEEE Std P1073.3.3/D8 Unapproved IEEE Draft Standard for Health Informatics - Point-Of Care Medical Device Communication - Transport Profile - IRDA - Infrared Wireless
  • IEEE/ISO 11073-10207-2019 ISO/IEEE International Standard - Health informatics--Point-of-care medical device communication - Part 10207: Domain Information and Service Model for Service-Oriented Point-of-Care Medical Device Communication
  • ISO/IEEE 11073-10207:2019(E) ISO/IEC/IEEE Health informatics--Point-of-care medical device communication Part 10207: Domain Information and Service Model for Service-Oriented Point-of-Care Medical Device Communication
  • IEEE Std 1073.3.1-1994 IEEE Standard for Medical Device Communications-Transport Profile-Connection Mode
  • IEEE P1847/D2, August 2019 IEEE Draft Recommended Practice for Common Framework of Location Services (LS) for Healthcare
  • IEEE P1073.1.1.1/D04:2002 Draft Standard for Health Informatics Point-of-Care Medical Device Communication, Nomenclature DS5902
  • IEEE P1073.1.1.1/D05D:2002 Draft Standard for Health Informatics Point-of-Care Medical Device Communication, Nomenclature DS5902
  • IEEE P1847/D1, Mar 2019 IEEE Draft Recommended Practice for Common Framework of Location Services (LS) for Healthcare
  • IEEE P11073-20702/D7, August 2016 IEEE Approved Draft Standard for Medical Devices Communication Profile for Web Services
  • IEEE P11073-20702/D5, March 2016 IEEE Draft Standard for Medical Devices Communication Profile for Web Services
  • IEEE P11073-20702/D6, July 2016 IEEE Draft Standard for Medical Devices Communication Profile for Web Services
  • IEEE Std 1073.3.2-2000 IEEE Standard for Medical Device Communications - Transport Profile - IrDA Based - Cable Connected
  • IEEE 11073-10101-2019 IEEE Standard for Health informatics--Point-of-care medical device communication - Part 10101: Nomenclature
  • IEEE Std 1073.1.1.1-2004 IEEE Standard for Health Informatics - Point-of-care medical device communication - Part 10101: Nomenclature
  • IEEE 1073.1.1.1-2004 IEEE Standard for Health Informatics - Point-of-care medical device communication - Part 10101: Nomenclature
  • IEEE Std 11073-10102-2012 Health informatics Point-of-care medical device communication Part 10102: Nomenclature Annotated ECG
  • IEEE Std 11073-10101-2019 IEEE Standard for Health informatics--Point-of-care medical device communication - Part 10101: Nomenclature
  • ISO/IEEE 11073-10101:2004(E) ISO/IEEE Health informatics -- Point-of-care medical device communication -- Part 10101: Nomenclature

Danish Standards Foundation, medical access

  • DS/ISO/TS 22421:2021 Sterilization of health care products – Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
  • DS-hæfte 14:2000 Communication and exchange of healthcare records
  • DS/EN 1789+A1:2010 Medical vehicles and their equipment - Road ambulances
  • DS/CEN/CR 14301:2002 Health informatics - Framework for security protection of healthcare communication
  • DS/ISO/TS 37137-1:2021 Biological evaluation of absorbable medical devices – Part 1: General requirements
  • DS/EN ISO 11073-10101:2005 Health informatics - Point-of-care medical device communication - Part 10101: Nomenclature
  • DS/ENV 1064:1993 Medical informatics. Standard communication protocol. Computer-assisted electrocardiography
  • DS/IEC/TR 80001-2-2:2012 Application of risk management for IT-networks incorporating medical devices - Part 2-2: Guidance for the disclosure and communication of medical device security needs, risks and controls
  • DS/EN 60601-1-4:1998 Medical electrical equipment - Part 1: General requirements for safety - 4. Collateral Standard: Programmable electronical medical systems
  • DS/EN ISO 11073-10201:2005 Health informatics - Point-of-care medical device communication - Part 10201: Domain information model

American Society of Heating, Refrigerating and Air-Conditioning Engineers (ASHRAE), medical access

American National Standards Institute (ANSI), medical access

  • ANSI P1073.1.3.7/D4.0-1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized – Blood Pressure
  • ANSI P1073.1.3.8/D4.0-1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized – Temperature
  • ANSI P1073.1.3.6/D6.0-1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - ECG
  • ANSI P1073.1.3.10/D3.0-1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized – Cardiac Output
  • ANSI P1073.1.3.9/D3.0-1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized – Airway Flow
  • ANSI P1073.1.3.5/D04-2000 Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Defibrillator Device
  • ANSI P1073.1.3.11/D3.0-1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized – Capnometer
  • ANSI/IEEE 11073-00101:2008 Guide for Health Informatics - Point-of-Care Medical Device Communication - Technical Report - Guidelines for the Use
  • ANSI/TIA-1179-2010 Healthcare Facility Telecommunications Infrastructure Standard
  • ANSI/AAMI/IEC 60601-1-8:2013 Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
  • ANSI/IEEE 11073-10101:2004 Standard for Health Informatics - Point-of-Care Medical Device Communication - Nomenclature
  • ANSI P1073.1.1.1/D08-2003 Draft Standard for Health informatics – Point-of-care medical device communication – Nomenclature

Shandong Provincial Standard of the People's Republic of China, medical access

Lithuanian Standards Office , medical access

AT-ON, medical access

IT-UNI, medical access

  • UNI EN 1789-2021 Medical vehicles and their equipment - Road ambulances
  • UNI ISO 18250-1:2021 Medical devices -- Connectors for reservoir delivery systems for healthcare applications - Part 1: General requirements and common test methods

CEN - European Committee for Standardization, medical access

  • PREN 1789-2018 Medical vehicles and their equipment - Road ambulances
  • EN ISO 11073-10101:2005 Health informatics - Point-of-care medical device communication - Part 10101: Nomenclature
  • PREN 13608-3-2005 Health informatics - Security for healthcare communication - Part 3: Secure data channels

ES-UNE, medical access

  • UNE-EN 1789:2021 Medical vehicles and their equipment - Road ambulances
  • UNE-EN ISO 11073-20701:2020 Health informatics - Device interoperability - Part 20701: Point-of-care medical device communication - Service oriented medical device exchange architecture and protocol binding (ISO/IEEE 11073-20701:2020) (Endorsed by Asociación Española de Normali...

AENOR, medical access

  • UNE-EN 1789:2007+A2:2015 Medical vehicles and their equipment - Road ambulances
  • UNE-EN 13532:2002 General requirements for in vitro diagnostic medical devices for self-testing.
  • UNE-EN 60601-1-4/A1:2000 Medical electrical equipment -- Part 1-4: General requirements for safety - Collateral standard: Programmable electrical medical systems

RU-GOST R, medical access

  • GOST R 56044-2014 Evaluation of medical technologies. General regulations
  • GOST R 57298-2016 Radiopharmaceutical medicinal products. General requirements for organization of production of radiopharmaceuticals in medical organizations
  • GOST R 50444-1992 Medical instruments, apparatus and equipment. General specifications
  • GOST R 52921-2008 Medical maximum glass thermometers. General specifitications
  • GOST R IEC 60336-1999 X-ray tube assemblies for medical diagnosis. Characteristics of focal spots
  • GOST R ISO 15223-1-2014 Medical devices. Symbols to be used with medical device labels, labelling, and information to be supplied. Part 1. General requirements
  • GOST R 56328-2014 Medical equipment. Mobile complexes for medical purpose. General specifications and test methods
  • GOST R 55082-2012 Articles of paper for medical purposes. Diapers for adults. General specifications
  • GOST R 57765-2017 Medical equipment. Products prosthetic-orthopedic. General technical requirements
  • GOST R 57765-2021 Prosthetic-orthopedic products. General technical requirements
  • GOST 34243-2017 Telemedicine systems. General requirements for basic safety and essential performance of mobile telemedicine laboratory diagnostic kits
  • GOST 34244-2017 Telemedicine systems. General requirements for basic safety and essential performance of stationary telemedicine consultative and diagnostic centers
  • GOST 30324.0.4-2002 Medical electrical equipment. Part 1. General requirements for safety. 4. Safety requirements for programmable medical electrical systems
  • GOST 33459-2015 Medicine remedies for veterinary use. Vaccines against dermatophytosis of animals. General specification
  • GOST R 22.3.12-2016 Safety in emergencies. Medical means of individual protective. General technical requirements
  • GOST 31508-2012 Medical products. Classification in accordance with potential risk of using. General requirements
  • GOST R 55954-2014 Medical electrical equipment. Lung ventilators. Technical requirements for public procurement
  • GOST R 56841-2015 Application of risk management for IT-networks incorporating medical devices. Part 2-4. Application guidance. General implementation guidance for healthcare delivery organizations
  • GOST R ISO 14937-2012 Sterilization of health care products. General criteria for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
  • GOST R 56850-2015 Health infornatics. Risk management for IT-networks incorporating medical devices. Part 2-2. Guidance for the disclosure and communication of medical device security needs, risks and controls
  • GOST R 56842-2015 Health informatics. Point-of-care medical device communication. Part 10101. Nomenclature
  • GOST R 50267.12-2006 Medical electrical equipment. Part 2-12. Particular requirements for safety of lung ventilators for critical care ventilation
  • GOST R 50267.12-1993 Medical electrical equipment. Part 2. Particular requirements for the safety of lung ventilators for medical use

Taiwan Provincial Standard of the People's Republic of China, medical access

Guangdong Provincial Standard of the People's Republic of China, medical access

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, medical access

  • GB 27949-2011 General Requirements for Disinfectants for Medical Devices
  • GB/T 42204-2022 Communication specification for clinical medical equipment—Imaging equipment
  • GB/T 38800-2020(英文版) General technical requirements of modular isolation units for emergency medical use
  • GB 18282.1-2000 Sterilization of health care products--Chemical indicators--Part 1: General requirements
  • GB 18281.1-2000 Sterilization of health care products--Biological indicators--Part 1: General
  • GB 18282.1-2015 Chemical indicators for sterilization of healthcare products - part 1: general rules
  • GB 18281.1-2015 Sterilization of health care products.Biological indicators.Part 1:General requirements
  • GB/T 19974-2005 Sterilization of health care products.General requirement for characterization of a sterilization agent and the development,validation and routine control of a sterilization process for medical devices
  • GB/T 19974-2018 Sterilization of health care products.General requirement for characterization of a sterilization agent and the development, validation and routine control of a sterilization process for medical devices

国家市场监督管理总局、中国国家标准化管理委员会, medical access

  • GB 27949-2020 General requirements of disinfectant of medical instruments

Group Standards of the People's Republic of China, medical access

  • T/NAHIEM 92-2023
  • T/GDNS 002-2023 Health medical data compliance circulation standard
  • T/CAMDI 008-2016 General rules for the implementation of medical device manufacturing quality management regulations for sterile medical device manufacturing equipment
  • T/CACM 1212-2019 Clinical guidelines for diagnosis and treatment of gynecology in TCM postpartum urinary retention
  • T/CSEM 0015-2023 General Aviation Medical Rescue Emergency Plan Preparation Guidelines
  • T/GMIAAC 001-2022 Maintain code for ventilation and air conditioning systems of medical buildings
  • T/HENANPA 011-2023 Evaluation index system for calcium channel blocker drugs in medical institutions
  • T/GDPCIA 007-2023 Additive manufacturing — General specification for 3D printing devices for medical devices

SE-SIS, medical access

  • SIS SS-IEC 601-2-12:1991 Medical electrical equipment - Part 2: Particular requirements for the safety oflung ventilators for medical use

Professional Standard - Hygiene , medical access

  • WS/T 393-2012 Development and implementation of clinical pathways for medical institutions

CN-GJB-H, medical access

  • GJB 5515-2006 General specification for field mobile medical system
  • GJB 5515/10-2006 Detail specification for connecting shelter of field mobile medical system

American Society for Testing and Materials (ASTM), medical access

  • ASTM F1220-95(2006) Standard Guide for Emergency Medical Services System (EMSS) Telecommunications
  • ASTM F1220-95(2001) Standard Guide for Emergency Medical Services System (EMSS) Telecommunications
  • ASTM F1220-95(2022) Standard Guide for Emergency Medical Services System (EMSS) Telecommunications
  • ASTM F1220-95(2014) Standard Guide for Emergency Medical Services System 40;EMSS41; Telecommunications
  • ASTM F2076-01(2006) Standard Practice for Communicating an EMS Patient Report to Receiving Medical Facilities
  • ASTM F2076-01 Standard Practice for Communicating an EMS Patient Report to Receiving Medical Facilities
  • ASTM F2076-01(2014) Standard Practice for Communicating an EMS Patient Report to Receiving Medical Facilities
  • ASTM F2076-01(2022) Standard Practice for Communicating an EMS Patient Report to Receiving Medical Facilities

US-FCR, medical access

Japanese Industrial Standards Committee (JISC), medical access

  • JIS S 9623:2015 Medical care wig and accessory -- General specifications
  • JIS Z 4752-1:2001 Evaluation and routine testing in medical imaging departments -- Part 1: General aspect
  • JIS T 60601-1-8:2012 Medical electrical equipment -- Part 1-8: General requirements for basic safety and essential performance -- Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
  • JIS T 11140-1:2013 Sterilization of health care products.Chemical indicators.Part 1: General requirements

NZ-SNZ, medical access

  • AS/NZS 3200.1.8:2005 Medical electrical equipment Part 1.8: General requirements for safetyCollateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
  • AS/NZS 4580:1999 Medical Electrical Equipment - Digital Imaging and Communications in Medicine (DICOM) - Radiotherapy Objects

Professional Standard - Medicine, medical access

  • YY 0317-2000 General specifications for medical therapeutic X-ray equipment
  • YY/T 0317-2007 General specifications for medical therapeutic X-ray equipment
  • YY/T 0466.1-2009 Medical devices.Symbols to be used with medical device labels,labelling and information to be supplied.Part 1:General requirements
  • YY/T 0466.1-2016 Medical devices.Symbols to be used with medical device labels,labelling and information to be supplied.Part 1:General requirements
  • YY/T 0723-2009 Medical electrical equipment—Digital imaging and communications in medicine(DICOM)—Radiotherapy objects
  • YY/T 1441-2016 General requirements of performance evaluation of in vitro diagnostic medical devices
  • YY/T 0606.3-2007 Tissue engineered medical products.Part 3:General classification
  • YY/T 0567.1-2005 Aseptic processing of health care products - Part 1: General requirements
  • YY/T 0567.1-2013 Aseptic processing of health care products.Part 1:General requirements
  • YY/T 1842.1-2022
  • YY/T 0878.2-2015 Test for complement activation of medical devices.Part 2:Serum alternative pathway complement activation
  • YY/T 1914-2023 General requirements for medical devices and appliances used in human assisted reproductive technology

(U.S.) Telecommunications Industries Association , medical access

  • TIA-1179-2010 Healthcare Facility Telecommunications Infrastructure Standard

Canadian Standards Association (CSA), medical access

  • CSA C22.2 No.125-M1984-1984 Electromedical Equipment General Instruction No 1-2
  • CSA C22.2 No.60601-1-8-05-2005 Medical electrical equipment Part 1-8: General requirements for safety Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems First Edition; IEC 60601-1-8:200
  • CSA ISO 14937-01-CAN/CSA:2001 Sterilization of Health Care Products - General Requirements for Characterization of a Sterilizing Agent and the Development, Validation and Routine Control of a Sterilization Process for Medical Devices First Edition; ISO 14937:2000
  • CAN/CSA-ISO 14937:2011 Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (Second Edition)
  • CSA C22.2 No.60601-1-1-02-2002 Medical Electrical Equipment - Part 1-1: General Requirements for Safety - Collateral Standard: Safety Requirements for Medical Electrical Systems Second Edition [Superseded: CSA C22.2 NO 114-M90-CAN/CSA]
  • CSA C22.2 No.60601-1-4-02-2002 Medical Electrical Equipment - Part 1-4: General Requirements for Safety - Collateral Standard: Programmable Electrical Medical Systems First Edition
  • CSA C22.2 No.601.2.28-CAN/CSA-1994 Appareils Electromedicaux - Partie 2: Regles Particulieres De Securite Pour Les Ensembles Radiogenes A Rayonnement X Et Les Gaines Equipees Pour Diagnostic Medical Premiere Edition; Fiche No 1
  • CSA C22.2 No.601.2.28-CAN/CSA-94-1994 Medical Electrical Equipment - Part 2: Particular Requirements for the Safety of X-Ray Source Assemblies and X-Ray Tube Assemblies for Medical Diagnosis First Edition; General Instruction No 1
  • CSA Z317.2-01 UPD 2-2008 Special Requirements for Heating, Ventilation, and Air Conditioning (HVAC) Systems in Health Care Facilities

Standard Association of Australia (SAA), medical access

  • AS 2385:1990 Single-use (sterile) infusion sets for general medical use

North Atlantic Treaty Organization Military Agency for Standardization (NATO-MAS), medical access

  • STANAG 2562-2020 MEDICAL COMMUNICATIONS AND INFORMATION SYSTEMS (MedCIS) - AJMedP-5 EDITION B

GOSTR, medical access

  • GOST R EN 13532-2010 General requirements for in vitro diagnostic medical devices for self-testing
  • GOST R ISO 15223-1-2020 Medical devices. Symbols to be used with medical device labels, labelling, and information to be supplied. Part 1. General requirements

Heilongjiang Provincial Standard of the People's Republic of China, medical access

  • DB23/T 2785-2020 Medical institutions provide green channel service specifications for the elderly to seek medical treatment

Indonesia Standards, medical access

  • SNI 16-6642-2002 Medical equipment single use winged intravenous devices (sterile) for general medical use

BR-ABNT, medical access

  • ABNT NBR ISO 15223-1:2010 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied Part 1- General requirements

Jilin Provincial Standard of the People's Republic of China, medical access

  • DB22/T 3248-2021 TCM diagnosis and treatment norms for acute bacterial lower urinary tract infection in children

International Electrotechnical Commission (IEC), medical access

  • IEC TR3 61852:1998 Medical electrical equipment - Digital imaging and communications in medicine (DICOM) - Radiotherapy objects
  • IEC 60601-1-8:2012 Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
  • IEC 60601-1-11:2015 Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
  • IEC 60601-1-1/AMD1:1995 Medical electrical equipment - Part 1: General requirement for safety - 1. Collateral standard: Safety requirements for medical electrical systems; Amendment 1
  • IEC 60601-2-12:1988 Medical electrical equipment; part 2: particular requirements for the safety of lung ventilators for medical use

Korean Agency for Technology and Standards (KATS), medical access

  • KS C IEC 61852:2007 Medical electrical equipment-Digital imaging and communications in medicine(DICOM)-Radiotherapy objects
  • KS C IEC 61852-2007(2017) Medical electrical equipment-Digital imaging and communications in medicine(DICOM)-Radiotherapy objects
  • KS C IEC 60601-1-11:2012 Medical electrical equipment-Part 1-11:General requirements for basic safety and essential performance-Collateral Standard:Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment
  • KS X ISO/IEEE 11073-10101-2015(2020) Health informatics — Point-of-care medical device communication — Part 10101: Nomenclature
  • KS C IEC 60601-1-4:2002 Medical electrical equipment-Part 1-4: General requirement for safety-Collateral standard:Programmable electrical medical systems
  • KS P ISO 13408-1:2010 Aseptic processing of health care products-Part 1:General requirements
  • KS P ISO 14155-1:2007 Clinical investigation of medical devices for human subjects-Part 1:General requirements
  • KS P ISO 13408-1:2017 Aseptic processing of health care products-Part 1:General requirements
  • KS C IEC 60601-1-8:2005 Medical electrical equipment-Part 1-8:Generalrequirements for safety-Collateral standard:General requirements, tests and guidance for alarm systems inmedical electrical equipment and medical electrical systems
  • KS X ISO TR 21730-2015(2020) Health informatics-Use of mobile wireless communication and computing technology in healthcare facilities-Recommendations for the management of unintentional electromagnetic interference with medical
  • KS X IEC TR 80001-2-2-2015(2020) Application of risk management for IT-networks incorporating medical devices — Part 2-2: Guidance for the disclosure and communication of medical device security needs, risks and controls
  • KS X IEC TR 80001-2-2:2015 Application of risk management for IT-networks incorporating medical devices — Part 2-2: Guidance for the disclosure and communication of medical device security needs, risks and controls
  • KS X ISO/IEEE 11073-10201:2015 Health informatics — Point-of-care medical device communications — Part 10201: Domain information model
  • KS X ISO/IEEE 11073-10201-2015(2020) Health informatics — Point-of-care medical device communications — Part 10201: Domain information model

US-AAMI, medical access

  • ANSI/AAMI/ISO 15223-1:2007 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements

Tianjin Provincial Standard of the People's Republic of China, medical access

  • DB12/T 1016-2020 General requirements for design and implementation of medical device traceability system

国家食品药品监督管理局, medical access

  • YY/T 0507.1-2005 Sterile processing of medical products Part 1: General requirements

IEC - International Electrotechnical Commission, medical access

  • IEC TR 61852:1998 Medical Electrical Equipment - Digital Imaging and Communications in Medicine (DICOM) - Radiotherapy Objects (Edition 1.0)

CN-STDBOOK, medical access

  • 图书 A-4775 Digital China——Smart medical care and elderly care model and high-quality practice path

Jiangsu Provincial Standard of the People's Republic of China, medical access

  • DB32/T 3764-2020 General technical specification for sample preparation of medical sewage virus detection

UNKNOWN, medical access

  • GB/T 18282.1-2015 Chemical Indicators for Sterilization of Healthcare Products Part 1: General Rules

International Telecommunication Union (ITU), medical access

NATO - North Atlantic Treaty Organization, medical access

  • AJMEDP-5-2013 ALLIED JOINT DOCTRINE FOR MEDICAL COMMUNICATIONS AND INFORMATION SYSTEMS (MedCIS) (ED A@ Ver 1)

Professional Standard - Public Safety Standards, medical access

  • GA/T 1088-2013 Criteria of treatment time for the injured in road traffic accidents
  • GA/T 1088-2021 End time of treatment for injured persons in road traffic accidents

IX-EU/EC, medical access

  • TEST/92/42-1996 List of Bodies Notified under Directive 92/42/EEC Hot-Water Boilers
  • TEST/93/42-1996 List of Bodies Notified under Directive 93/42/EEC Medical Devices
  • COM(2003) 73 FINAL-2003 COMMUNICATION FROM THE COMMISSION concerning the introduction of a European health insurance card

ITU-R - International Telecommunication Union/ITU Radiocommunication Sector, medical access

  • REPORT SM.2180-2010 Impact of industrial@ scientific and medical (ISM) equipment on radiocommunication services

ITU-T - International Telecommunication Union/ITU Telcommunication Sector, medical access

  • ITU-T X.1080.1-2018 e-Health and world-wide telemedicines – Generic telecommunication protocol (Study Group 17)

KR-KS, medical access

  • KS P ISO 8536-10-2017 Infusion equipment for medical use-Part 10:Accessories for fluid lines for use with pressure infusion equipment

ETSI - European Telecommunications Standards Institute, medical access

  • TR 102 732-2013 Machine-to-Machine Communications (M2M); Use Cases of M2M applications for eHealth (V1.1.1)

Sichuan Provincial Standard of the People's Republic of China, medical access

  • DB51/T 1768.2-2018 General Technical Requirements for Textile Products for Public Use Part 2 For Non-medical Places




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