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Database: 365,228(8 Aug 2026)

Medical Equipment Parameters

Medical Equipment Parameters, Total:352 items.

The international standard classification for "Medical Equipment Parameters" includes: IT applications in health care technology , Therapy equipment .

The Chinese standard classification for "Medical Equipment Parameters" includes: Computer application , Medical radiographic equipment , Marking, packaing, transport and storage .


Professional Standard - Post and Telecommunication

  • YD/T 4899-2024 Technical requirements for medical equipment management platform for digital hospitals

Military Standard of the People's Republic of China-General Armament Department

Group Standards of the People's Republic of China

  • T/CSBME 036-2021 Guidelines for Environmental Profile Parameters of Medical Electrical Equipment
  • T/CSBME 025-2021 Reliability Management System of Medical Equipment
  • T/JCCIA 004-2022 Specification for debugging network equipment in data centers in the medical industry
  • T/CHAS 10-3-4-2019 Quality and safety management of Chinese hospital—Part 3-4: Medical service support —Medical device
  • T/CAS 842-2024 Evaluation of quality management maturity of medical equipment in medical institutions
  • T/GDNS 001-2022 Safety code for medical devices

Jiangsu Provincial Standard of the People's Republic of China

  • DB32/T 3549-2019 Specifications for setting up facilities and equipment for temporary storage of medical waste in medical and health institutions

Jiangxi Provincial Standard of the People's Republic of China

  • DB36/T 609-2011 RFID Equipment Technical Criterion for Health Care Application

General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China

  • GB/T 42204-2022 Communication specification for clinical medical equipment—Imaging equipment

Taiwan Provincial Standard of the People's Republic of China

  • CNS 12491.13-1989 Graphical Symbols for Use on Electrical and Electronic Equipment (Medical Equipment)
  • CNS 12491-13-1989 Graphical Symbols for Use on Electrical and Electronic Equipment (Medical Equipment)

Professional Standard - Medicine

  • YY/T 0083-1992 Product nameplate for medical instruments and equipment
  • YY/T 0723-2009 Medical electrical equipment—Digital imaging and communications in medicine(DICOM)—Radiotherapy objects
  • YY 0083-1992 Product nameplate for medical equipment

National Metrological Technical Specifications of the People's Republic of China

  • JJF 1972-2022 Calibration Specification for Performance Parameters for Medical Cabin of Negative Pressure Ambulances

Professional Standard - Commodity Inspection

  • SN/T 1430.1-2004 Rules for the inspection of medical electrical equipment for improt - Ultrasonic medical diagnostic and therapy equipment

Institute of Electrical and Electronics Engineers (IEEE)

  • IEEE P1073.1.3.5/D04:2000 Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Defibrillator Device
  • IEEE P1073.1.3.7/D4.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Blood Pressure
  • IEEE P1073.1.3.11/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 P1073.1.3.8/D4.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Temperature
  • 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 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 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
  • 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 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 P1073.1.3.5/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 P1073.1.3.7/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 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 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 Std P1073.2.0/D0.05 Proposed Draft IEEE Standard - Medical Device Communications - Medical Device Application Profiles (MDAP) - Base Standard
  • IEEE P11073-10701/D4, March 2022 IEEE Draft Standard for Health Informatics - Device Interoperability - Part 10701: Point-of-Care Medical Device Communication - Metric Provisioning by Participants in a Service-Oriented Device Connectivity (SDC) System
  • IEEE P11073-10701/D3, October 2021 IEEE Draft Standard for Health Informatics - Device Interoperability - Part 10701: Point-of-Care Medical Device Communication - Metric Provisioning by Participants in a Service-Oriented Device Connectivity (SDC) System

International Organization for Standardization (ISO)

German Institute for Standardization

  • DIN EN ISO 15225 E:2015-08 Medical device quality management medical device nomenclature data structure (draft)
  • DIN EN 62366:2008 Medical devices - Application of usability engineering to medical devices (IEC 62366:2007); German version EN 62366:2008
  • DIN EN ISO 14971:2007 Medical devices - Application of risk management to medical devices (ISO 14971:2007); German version EN ISO 14971:2007
  • DIN EN 556-1:2002 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; German version EN 556-1:2001
  • DIN EN 1640:2010-02 Dentistry - Medical devices for dentistry - Equipment; German version EN 1640:2009
  • DIN EN ISO 15225:2010 Medical devices - Quality management - Medical device nomenclature data structure (ISO 15225:2010); German version EN ISO 15225:2010
  • DIN EN ISO 15225:2016 Medical devices - Quality management - Medical device nomenclature data structure (ISO 15225:2016); German version EN ISO 15225:2016
  • DIN EN 62353:2008 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment (IEC 62353:2007); German version EN 62353:2008
  • DIN EN 1639:2010-02 Dentistry - Medical devices for dentistry - Instruments; German version EN 1639:2009
  • DIN EN IEC 62667:2020 Medical electrical devices – Medical light ion irradiation devices – Apparatus quality characteristics (IEC 62667:2017)
  • DIN EN ISO 19054:2006 Rail systems for supporting medical equipment (ISO 19054:2005); English version of DIN EN ISO 19054:2006-09

CZ-CSN

  • CSN 85 2104-1982 Anaesthetic and breaíhing apparatuses, medical. Technical parameters and testing methods
  • CSN 85 6009-1980 Medical apparatus. Dental technics. Symbols

British Standards Institution (BSI)

  • BS EN 62464-1:2007 Magnetic resonance equipment for medical imaging - Determination of essential image quality parameters
  • BS EN ISO 14971:2007 Medical devices - Application of risk management to medical devices
  • BS EN 62366:2008 Medical devices - Application of usability engineering to medical devices
  • PD ISO/TR 25555:2024 Ageing societies. Accessibility and usability considerations for home healthcare products, related services and environments
  • BS ISO 24163-2:2024 Clamp-in tyre valves for tyre pressure monitoring systems - Test methods and performance
  • BS EN 13824:2004 Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements
  • BS PD IEC/TR 60601-4-1:2017 Medical electrical equipment. Guidance and interpretation. Medical electrical equipment and medical electrical systems employing a degree of autonomy
  • BS EN 556-2:2004 Sterilization of medical devices. Requirements for medical devices to be designated "STERILE". Requirements for aseptically processed medical devices
  • BS EN ISO 10079-1:2015 Medical suction equipment. Electrically powered suction equipment
  • BS EN ISO 10079-2:2022 Medical suction equipment. Manually powered suction equipment
  • BS EN 62353:2014 Medical electrical equipment. Recurrent test and test after repair of medical electrical equipment
  • BS EN 62353:2008 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment
  • BS EN ISO 10079-2:2000 Medical suction equipment - Manually powered suction equipment
  • PD IEC/TR 60601-4-2:2016 Medical electrical equipment. Guidance and interpretation. Electromagnetic immunity: performance of medical electrical equipment and medical electrical systems
  • BS EN ISO 10079-2:1997 Medical suction equipment. Manually powered suction equipment
  • BS EN ISO 10079-1:2015+A1:2019 Medical suction equipment. Electrically powered suction equipment
  • BS EN ISO 10079-1:2022 Medical suction equipment. Electrically powered suction equipment
  • BS EN 12286:1999 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures
  • BS EN 12286:1999(2001) In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures
  • BS EN 556-1:2001 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Requirements for terminally sterilized medical devices
  • BS EN IEC 62667:2018 Medical electrical equipment. Medical light ion beam equipment. Performance characteristics
  • BS EN 15986:2011 Symbol for use in the labelling of medical devices. Requirements for labelling of medical devices containing phthalates
  • DD ENV 12611-1998 Medical informatics. Categorical structure of systems of concepts. Medical devices
  • BS EN 60601-2-3:1993 Medical electrical equipment. Particular requirements for safety. Specification for short-wave therapy equipment
  • BS EN 60601-2-3:1992 Medical electrical equipment. Particular requirements for safety. Specification for short-wave therapy equipment
  • PD CEN ISO/TR 24971:2020 Medical devices. Guidance on the application of ISO 14971
  • BS EN ISO 10079-3:1997 Medical suction equipment. Suction equipment powered from vacuum or pressure source
  • BS EN ISO 9170-1:2008 Terminal units for medical gas pipeline systems - Terminal units for use with compressed medical gases and vacuum
  • BS EN 60976:2008 Medical electrical equipment - Medical electron accelerators - Functional performance characteristics
  • BS EN 60976:2007 Medical electrical equipment - Medical electron accelerators - Functional performance characteristics
  • BS EN ISO 10079-3:2000 Medical suction equipment - Suction equipment powered from a vacuum or pressure source
  • BS DD ISO/TS 10993-20:2006 Biological evaluation of medical devices - Principles and methods for immunotoxicology testing of medical devices
  • BS EN 60601-1-12:2015+A1:2020 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…
  • PD IEC TR 60788:2004 Medical electrical equipment. Glossary of defined terms
  • 18/30370883 DC BS EN ISO 14971. Medical devices. Application of risk management to medical devices
  • BS EN ISO 19054:2006+A1:2016 Rail systems for supporting medical equipment
  • BS ISO 28620:2020 Medical devices. Non-electrically driven portable infusion devices
  • PD IEC/TR 80002-1:2009 Medical device software. Guidance on the application of ISO 14971 to medical device software

SCC

  • DANSK DS/IEC TR 80002-3:2014 Medical device software - Part 3: Process reference model of medical device software life cycle processes
  • AAMI EQ93:2019 Medical equipment management - Vocabulary used in medical equipment programs
  • CSA C22.2 No.125-1979 Electromedical equipment
  • CSA C22.2 No.125-M1984-1984(R2004) Electromedical Equipment
  • CSA C22.2 No.125-1973 Electro-Medical Equipment
  • CSA C22.2 No.125-M1984-1984(C2004) Electromedical equipment
  • BS EN 1640:1997 Dentistry. Medical devices for dentistry. Equipment
  • DANSK DS/EN 1640:2009 Dentistry - Medical devices for dentistry - Equipment
  • AENOR UNE-EN ISO 15225:2016 Medical devices. Quality management. Structure of nomenclature data for medical devices. (ISO 15225:2016).
  • DANSK DS/EN 62366-1/A1:2020 Medical devices – Part 1: Application of usability engineering to medical devices
  • DANSK DS/EN 62366-1/AC:2019 Medical devices – Part 1: Application of usability engineering to medical devices
  • ISO 13485:2016 - Medical Devices - A Practical Guide Medical devices - A practical guide
  • BS EN 60601-2-33:1996 Medical electrical equipment. Particular requirements for safety-Specification for magnetic resonance equipment for medical diagnosis
  • BS PD IEC/TR 60601-4-2:2016 Medical electrical equipment-Guidance and interpretation. Electromagnetic immunity: performance of medical electrical equipment and medical electrical systems
  • CEI 62-17:1998 Electrical medical equipment - Special safety regulations for microwave therapy equipment
  • DANSK DS/IEC TR 62366-2:2016 Medical devices – Part 2: Guidance on the application of usability engineering to medical devices
  • AAMI/IEC TIR80002-1:2009 Medical device software - Part 1: Guidance on the application of ISO 14971 to medical device software
  • DANSK DS/IEC/TR 80002-1:2009 Medical device software - Part 1: Guidance on the application of ISO 14971 to medical device software
  • DIN EN 62366 E:2006 Draft Document - Medical devices - Application of usability engineering to medical devices (IEC 62A/535/CDV:2006); German version prEN 62366:2006
  • BS EN 62366:2008+A1:2015 Medical devices. Application of usability engineering to medical devices
  • NS-EN 1640:2004 Dentistry — Medical devices for dentistry — Equipment
  • NS-EN 1640:2009 Dentistry — Medical devices for dentistry — Equipment
  • BS 5724-2-2.3:1983 Medical electrical equipment. Particular requirements for safety-Specification for short wave therapy equipment
  • NS-EN 1639:2009 Dentistry — Medical devices for dentistry — Instruments
  • BS EN 1641:1997 Dentistry. Medical devices for dentistry. Materials
  • BS PD ISO/TR 24971:2013 Medical devices. Guidance on the application of ISO 14971
  • NS-EN 1640:1996 Dentistry — Medical devices for dentistry — Equipment
  • DANSK DS/IEC TR 60601-4-2:2016 Medical electrical equipment – Part 4-2: Guidance and interpretation – Electromagnetic immunity: performance of medical electrical equipment and medical electrical systems
  • DANSK DS/EN 1639:2009 Dentistry - Medical devices for dentistry - Instruments
  • BS PD ISO/TR 24971:2020 Medical devices. Guidance on the application of ISO 14971
  • BS PD CEN ISO/TR 24971:2020 Medical devices. Guidance on the application of ISO 14971
  • BS 5724-2.14:1989 Medical electrical equipment. Particular requirements for safety-Specification for electroconvulsive therapy equipment
  • CAN/CSA-Z9919-2007(C2012) Electromedical devices - Special safety rules and essential performance of equipment used for pulse oximeters for medical use
  • CSA Z387-2013(R2018) Safe use of electrosurgical medical devices and systems in health care
  • DIN EN 60601-1-11 E:2014 Draft Document - 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 e...
  • DIN EN 60601-1-11/A1 E:2018 Draft Document - 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 e...
  • DIN IEC 60601-1-11 E:2008 Draft Document - 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 e...
  • CAN/CSA-IEC 62366-2014 Medical devices - Application of usability engineering to medical devices (Adopted IEC 62366:2007, first edition, 2007-10)
  • AAMI TIP24:1999 Acquisition and use of physiologic waveform databases for testing of medical devices
  • DANSK DS/EN ISO 19054/A1:2006 Rail systems for supporting medical equipment
  • CSA C22.2 No.121-1959 Electric Heating Equipment for Medical and Dental Use
  • CSA DIR.003-1998 List of CSA Certified Health Care Equipment
  • DANSK DS/EN ISO 19054:2006 Rail systems for supporting medical equipment
  • DIN EN 62366-1/A1 E:2019 Draft Document - Medical devices - Part 1: Application of usability engineering to medical devices (IEC 62A/1288/CDV:2018); German and English version EN 62366-1:2015/prA1:2018
  • BS 5724-2-2.11:1989 Medical electrical equipment. Particular requirements for safety-Specification for gamma beam therapy equipment
  • DIN EN 62366-1 E:2014 Draft Document - Medical devices - Part 1: Application of usability engineering to medical devices (IEC 62A/900A/CDV:2014); German version FprEN 62366-1:2013

American National Standards Institute (ANSI)

Association Francaise de Normalisation

  • NF C74-054:2008 Medical devices - Application of usability engineering to medical devices.
  • NF EN IEC 62667:2018 Medical electrical devices - Light ion beam medical devices - Performance characteristics
  • NF C74-309:1973 ELECTROMEDICAL EQUIPMENT ACTINOLOGY APPARATUS
  • NF EN 1640:2009 Art dentaire - Dispositifs médicaux pour l'art dentaire - Matériel
  • NF C74-157:2007 Magnetic resonance equipment for medical imaging - Part 1 : determination of essential image quality parameters.
  • NF C74-054-1*NF EN 62366-1:2015 Medical devices - Part 1 : application of usability engineering to medical devices
  • NF EN 62366-1/A1:2020 Medical devices - Part 1: application of usability engineering to medical devices
  • NF EN 62366-1:2015 Medical devices - Part 1: application of usability engineering to medical devices
  • NF C74-053*NF EN 62353:2015 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment
  • NF C74-053:2008 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment.
  • NF EN 62353:2015 Appareils électromédicaux - Essai récurrent et essai après réparation d'un appareil électromédical
  • NF EN ISO 17664-1:2021 Processing of healthcare products - Information relating to the processing of medical devices to be provided by the device manufacturer - Part 1: critical and semi-critical medical devices
  • NF S90-316:1987 Medico-surgical equipment. Operating tables.
  • NF C15-211:2006 Low-voltage electrical installations - Installations in medically used rooms
  • NF EN ISO 17664-2:2023 Processing of healthcare products - Information relating to the processing of medical devices to be provided by the device manufacturer - Part 2: non-critical medical devices
  • NF ISO 17664-2:2021 Processing of healthcare products - Information relating to the processing of medical devices to be provided by the device manufacturer - Part 2: non-critical medical devices
  • NF C74-122/A2:2008 Medical electrical equipment - Part 2-33 : particular requirements for the safety of magnetic resonance equipment for medical diagnosis.
  • NF EN 1639:2009 Art dentaire - Dispositifs médicaux pour l'art dentaire - Instruments
  • NF S90-202:1990 Medico-surgical equipment . Infusion sets.
  • NF EN 1641:2009 Art dentaire - Dispositifs médicaux pour l'art dentaire - Produits
  • NF EN ISO 19054:2006 Support rail systems for medical devices
  • NF S98-116:2004 Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices.
  • NF S90-201:1990 Medico-surgical equipment. Transfusion sets.
  • NF C74-208/A1:2001 Medical electrical equipment - Medical electron accelerators - Functional performance characteristics.
  • NF C74-122:1996 Medical electrical equipment. Part 2 : particular requirements for the safety of magnetic resonance equipment for medical diagnosis.
  • NF S97-317:1998 Rail systems for supporting medical equipment.
  • NF S91-300*NF EN 1640:2009 Dentistry - Medical devices for dentistry - Equipment
  • NF S97-317/A1:2002 Rail systems for supporting medical equipment.
  • NF S95-317*NF EN ISO 19054:2006 Rail systems for supporting medical equipment

GSO

  • GSO IEC 62366:2014 Medical devices - Application of usability engineering to medical devices
  • GSO IEC/TR 80002-3:2015 Medical device software - Part 3: Process reference model of medical device software life cycle processes (IEC 62304)
  • OS GSO IEC/TR 80002-3:2015 Medical device software - Part 3: Process reference model of medical device software life cycle processes (IEC 62304)
  • BH GSO IEC/TR 80002-3:2017 Medical device software - Part 3: Process reference model of medical device software life cycle processes (IEC 62304)
  • GSO IEC 62366-1:2015 Medical devices - Part 1: Application of usability engineering to medical devices
  • OS GSO IEC 62366-1:2015 Medical devices - Part 1: Application of usability engineering to medical devices
  • BH GSO IEC 62366-1:2017 Medical devices - Part 1: Application of usability engineering to medical devices
  • BH GSO IEC TR 62366-2:2022 Medical devices - Part 2: Guidance on the application of usability engineering to medical devices
  • GSO IEC TR 62366-2:2021 Medical devices - Part 2: Guidance on the application of usability engineering to medical devices
  • BH GSO IEC/TR 80002-1:2016 Medical device software - Part 1: Guidance on the application of ISO 14971 to medical device software
  • GSO IEC/TR 61852:2014 Medical electrical equipment - Digital imaging and communications in medicine (DICOM) - Radiotherapy objects
  • GSO EN 1639:2021 Dentistry — Medical devices for dentistry —Instruments
  • BH GSO EN 1641:2022 Dentistry. Medical devices for dentistry. Materials
  • BH GSO EN 1639:2022 Dentistry — Medical devices for dentistry —Instruments
  • GSO IEC TR 60601-4-2:2021 Medical electrical equipment - Part 4-2: Guidance and interpretation - Electromagnetic immunity: performance of medical electrical equipment and medical electrical systems
  • BH GSO IEC TR 60601-4-2:2022 Medical electrical equipment - Part 4-2: Guidance and interpretation - Electromagnetic immunity: performance of medical electrical equipment and medical electrical systems
  • GSO IEC/TR 80002-1:2015 Medical device software - Part 1: Guidance on the application of ISO 14971 to medical device software
  • GSO EN 1641:2021 Dentistry. Medical devices for dentistry. Materials

PL-PKN

RU-GOST R

  • GOST IEC 61157-2013 Medical electrical equipment. Devices for ultrasonic diagnostics. Requirements for the declaration of acoustic output parameters in technical documents
  • GOST R ISO 14971-2006 Medical devices. Application of risk management to medical devices
  • GOST R ISO 14971-2009 Medical devices. Application of risk management to medical devices
  • GOST R EN 556-1-2009 Sterilization of medical devices. Requirements for medical devices to be designated "sterile". Part 1. Requirements for terminally sterilized medical devices
  • GOST R 56331-2014 Medical electrical equipment. Medical diagnostic ultrasonic equipment. Technical requirements for governmental purchases
  • GOST R 57092-2016 Medical electrical equipment. Equipment for telemedicine videoconferencing. Technical requirements for governmental purchases
  • GOST R IEC/TR 60788-2009 Medical electrical equipment. Glossary
  • GOST R 50267.33-1999 Medical electrical equipment. Part 2. Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
  • GOST R IEC/TR 62266-2009 Medical electrical equipment. Guidelines for implementation of DICOM in radiotherapy
  • GOST R ISO 10993-12-1999 Medical devices. Biological evaluation of medical devices. Part 12. Sample preparation and reference materials
  • GOST R 56316-2014 Medical electrical equipment. Medical electron accelerators. Technical requirements for governmental purchases
  • GOST R ISO/TR 16142-2008 Medical devices. Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices
  • GOST R 58024-2017 Medical devices. Equipment for thermal disinfection/neutralization of medical waste. Dry hot air method. Technical requirements for governmental purchases

Spanish Association for Standardization (UNE)

  • UNE-EN 62366:2009 Medical devices- Application of usability engineering to medical devices
  • UNE-EN 1640:2004 Dentistry - Medical devices for dentistry - Equipment
  • UNE-EN 62366-1:2015 Medical devices - Part 1: Application of usability engineering to medical devices (Endorsed by AENOR in June of 2015.)
  • UNE-EN 62366-1:2015/A1:2020 Medical devices - Part 1: Application of usability engineering to medical devices (Endorsed by Asociación Española de Normalización in September of 2020.)
  • UNE-EN 62366-1:2015/AC:2015 Medical devices - Part 1: Application of usability engineering to medical devices (Endorsed by AENOR in February of 2016.)
  • UNE 20613-2-6:1988 MEDICAL ELECTRICAL EQUIPMENT. PARTICULAR REQUIREMENTS FOR THE SAFETY OF MICROWAVE THERAPY EQUIPMENT
  • UNE 20613-2-14:1993 MEDICAL ELECTRICAL EQUIPMENT. PARTICULAR REQUIREMENTS FOR THE SAFETY OF ELECTROCONSULSIVE THERAPY EQUIPMENT.
  • UNE-EN 1640:2010 Dentistry - Medical devices for dentistry - Equipment
  • IEC 60601-1:2023 SER Medical electrical equipment - ALL PARTS
  • UNE-EN 1639:2004 Dentistry - Medical devices for dentistry - Instruments
  • UNE-EN 60336:2006 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots

European Committee for Electrotechnical Standardization(CENELEC)

  • EN 62464-1:2007 Magnetic resonance equipment for medical imaging - Part 1: Determination of essential image quality parameters
  • EN 62366-1:2015 Medical devices - Part 1: Application of usability engineering to medical devices

PT-IPQ

  • NP EN 556-2000 Sterilization of medical devices Requirements for terminally sterilized medical devices to be labelled"Sterile"
  • NP EN 1441-2000 Medical devices Risk analysis
  • NP EN 12218-2000 Rail systems for supporting medical equipment

International Electrotechnical Commission (IEC)

  • IEC 80601-2-77:2023 Medical electrical equipment
  • IEC 62464-1:2007 Magnetic resonance equipment for medical imaging - Part 1: Determination of essential image quality parameters
  • IEC TR3 61852:1998 Medical electrical equipment - Digital imaging and communications in medicine (DICOM) - Radiotherapy objects
  • IEC 62366:2007+AMD1:2014 CSV Medical devices - Application of usability engineering to medical devices
  • IEC 62353:2007 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment
  • IEC 62353:2014 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment
  • IEC 60601-1:2024 SER Medical electrical equipment - ALL PARTS
  • IEC 60930:1988 Guidelines for administrative, medical, and nursing staff concerned with the safe use of medical electrical equipment
  • IEC TR 60930:2008 Guidelines for administrative, medical, and nursing staff concerned with the safe use of medical electrical equipment and medical electrical systems

Indonesia Standards

GB-REG

HU-MSZT

US-FCR

CEN - European Committee for Standardization

Korean Agency for Technology and Standards (KATS)

  • KS C IEC 61852:2007 Medical electrical equipment-Digital imaging and communications in medicine(DICOM)-Radiotherapy objects
  • KS C 1103-1990 Glossary of Terms Used in Medical Electrical Equipment (General Terms)
  • KS C IEC 62667:2019 Medical electrical equipment — Medical light ion beam equipment — Performance characteristics
  • KS C IEC 61852-2007(2017) Medical electrical equipment-Digital imaging and communications in medicine(DICOM)-Radiotherapy objects
  • KS A 4001-1989(2020) Graphical symbols for medical radiological equipment
  • KS C IEC 61852-2022 Medical electrical equipment-Digital imaging and communications in medicine(DICOM)-Radiotherapy objects
  • KS C IEC 60976:2020 Medical electrical equipment — Medical electron accelerators — Functional performance characteristics

Society of Automotive Engineers (SAE)

VN-TCVN

European Committee for Standardization (CEN)

RO-ASRO

Standard Association of Australia (SAA)

  • AS 2684:1984 Medical equipment - Humidifiers, for medical use
  • AS 2514:1981 Drying cabinets for medical equipment
  • AS 2514:1999 Drying cabinets for medical equipment
  • AS 1094:1993 Medical equipment - Single-use syringes (sterile) for general medical use
  • AS 2811:1985 Personal emergency medical information devices
  • AS 2696:1989 Medical equipment - Single-use urethral catheters (sterile) for general medical use
  • AS 2696:1984 Medical equipment - Single-use urethral catheters (sterile) for general medical use

Japanese Industrial Standards Committee (JISC)

  • JIS Z 4952:2012 Magnetic resonance equipment for medical imaging -- Part 1: Determination of essential image quality parameters
  • JIS T 2009:2005 Multiple medical device for home use
  • JIS Z 4701:1997 General rules for medical X-ray equipment

Underwriters Laboratories (UL)

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

Lithuanian Standards Office

  • LST EN 62366-2008 Medical devices - Application of usability engineering to medical devices (IEC 62366:2007)
  • LST EN 62353-2008 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment (IEC 62353:2007)
  • LST EN 1640-2010 Dentistry - Medical devices for dentistry - Equipment

GOST

  • GOST R IEC 62366-1-2023 Medical devices. Part 1. Application of usabilityengineering to medical devices
  • GOST R 70987-2023 Medical electrical equipment. Microwave therapy equipment. Technical condition control methods

SE-SIS

  • SIS SS IEC 601-2-6:1988 Medical electrical equipment — Particular requirements for the safety of microwave therapy equipment
  • SIS SS IEC 601-2-3:1988 Medical e/ectrical equipment — Particular requirements for the safety ofshort-wave therapy equipment
  • SIS SS 486 03 31-1990 Medical electrical equipment — Particular requirements for the safety of gamma beam therapy equipment
  • SIS SS-IEC 976:1991 Medical electrical equipment — Medical electron accelerators — Functionalperformance charactetistics
  • SIS SS-IEC 601-2-14:1991 Medical electrical equipment - Part 2: Particular requirements for the safety ofelectroconvulsive therapy equipment

US-AAMI

  • AAMI/IEC 62366-1:2015 Medical devices - Part 1 : Application of usability engineering to medical devices

Australian/New Zealand Standard (AU-AS/NZS)

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

  • 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

NATO - North Atlantic Treaty Organization

  • STANAG 7112-2011 RECOMMENDED MEDICAL EQUIPMENT FOR AEROMEDICAL EVACUATIONS (ED 1)

FI-SFS

KR-KS

  • KS C IEC 62667-2019 Medical electrical equipment — Medical light ion beam equipment — Performance characteristics
  • KS C IEC 60976-2020 Medical electrical equipment — Medical electron accelerators — Functional performance characteristics
  • KS C 3598-2018(2023) Medical electrical equipment ─ Glossary of defined terms

IX-EU/EC

GOSTR

DIN

Danish Standards Foundation

  • DS/EN 1640:2009 Dentistry - Medical devices for dentistry - Equipment
  • DS/EN 60336:2005 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots
  • DS/EN ISO 19054:2006 Rail systems for supporting medical equipment

American Society for Testing and Materials (ASTM)

  • ASTM F639-98a Standard Specification for Polyethylene Plastics for Medical Applications
  • ASTM F997-98a Standard Specification for Polycarbonate Resin for Medical Applications

Canadian Standards Association (CSA)

  • CSA Z387-2019 Safe use of electrosurgical medical devices and systems in health care
  • CSA DIR.003-99 List of CSA Certified Health Care Equipment

IEC - International Electrotechnical Commission

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

AT-ON

AT-OVE/ON

  • OVE EN 62366-1-2021 Medical devices - Part 1: Application of usability engineering to medical devices ( IEC 62366-1:2015) (german version)