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Database: 365,228(8 Aug 2026)

medical testing equipment

medical testing equipment, Total:153 items.

The international standard classification for "medical testing equipment" includes: Radiographic equipment .

The Chinese standard classification for "medical testing equipment" includes: Medical ultrasound, laser, high-frequency instrument and equipment .


Professional Standard - Commodity Inspection

  • SN/T 1672.6-2013 Rules for the inspection of import and export medical equipment - Part 6: Magnetic resonance imaging equipment for medical diagnosis
  • SN/T 1672.8-2013 Rules for the inspection of medical equipment for import and export - Part 8: Ultrasound diagnostic equipment and physiotherapy equipment
  • SN/T 1430.1-2004 Rules for the inspection of medical electrical equipment for improt - Ultrasonic medical diagnostic and therapy equipment

Shanxi Provincial Standard of the People's Republic of China

  • DB1407/T 52-2024 Safety Protection Guidelines for Medical Instrument and Equipment Inspection and Testing Personnel

国家质量监督检验检疫总局

  • SN/T 4445.1-2016 Technical requirements for the inspection of medical apparatus for import-Part 1: Medical electrical equipment

Professional Standard - Agriculture

  • SN/T 4445.3-2018 Technical requirements for the inspection of imported medical devices Part3 : Anaesthetic equipment

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

HU-MSZT

Association Francaise de Normalisation

  • NF S90-045:1985 Medico-surgical equipment. Aluminium caps for pharmaceutical use. Quality acceptance.
  • NF C74-053:2008 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment.
  • NF C74-053*NF EN 62353:2015 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment
  • 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 C74-235*NF EN 62274:2005 Medical electrical equipment - Safety of radiotherapy record and verify systems
  • NF EN 1640:2009 Art dentaire - Dispositifs médicaux pour l'art dentaire - Matériel
  • 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

British Standards Institution (BSI)

  • BS EN 62274:2005 Medical electrical equipment - Safety of radiotherapy record and verify systems
  • 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 14971:2007 Medical devices - Application of risk management to medical devices
  • BS EN 62366:2008 Medical devices - Application of usability engineering to medical devices
  • BS ISO 21474-2:2022 In vitro diagnostic medical devices. Multiplex molecular testing for nucleic acids - Validation and verification
  • 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 DD ISO/TS 10993-20:2006 Biological evaluation of medical devices - Principles and methods for immunotoxicology testing of medical devices
  • BS EN 13824:2004 Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements
  • BS PD IEC/TR 62354:2014 General testing procedures for medical electrical equipment
  • 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 11073-10101:2006 Health informatics - Point-of-care medical device communications - Nomenclature
  • BS EN ISO 10079-1:2015 Medical suction equipment. Electrically powered suction equipment
  • PD ISO/TR 19727:2017 Medical devices. Pump tube spallation test. General procedure
  • BS EN ISO 10079-2:2022 Medical suction equipment. Manually powered suction equipment

International Electrotechnical Commission (IEC)

  • 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 80601-2-77:2023 Medical electrical equipment
  • IEC 62366:2007+AMD1:2014 CSV Medical devices - Application of usability engineering to medical devices
  • IEC 62274:2005 Medical electrical equipment - Safety of radiotheraphy record and verify systems
  • IEC TR 62354:2009 General testing procedures for medical electrical equipment
  • IEC TR 62354:2014 General testing procedures for medical electrical equipment
  • IEC TR 62354:2005 General testing procedures for medical electrical equipment

German Institute for Standardization

  • 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 6846-5:1992 Medical teletherapy systems with gamma-emitting sources; constancy testing
  • DIN EN 62366:2008 Medical devices - Application of usability engineering to medical devices (IEC 62366:2007); German version EN 62366:2008
  • DIN EN 62274:2007 Medical electrical equipment - Safety of radiotherapy record and verify systems (IEC 62274:2005); German version EN 62274:2005
  • 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 E:2015-08 Medical device quality management medical device nomenclature data structure (draft)
  • DIN EN 62353:2015 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment (IEC 62353:2014); German version EN 62353:2014

International Organization for Standardization (ISO)

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

American National Standards Institute (ANSI)

  • ANSI/AAMI/IEC 62366:2007 Medical devices - Application of usability engineering to medical devices
  • AAMI TIR18:2010 Guidance on electromagnetic compatibility of medical devices in healthcare facilities

GSO

PL-PKN

SCC

CZ-CSN

  • CSN 84 7107-1988 Medical equipment. Formaldehyde sterilizers. General technical requirements and tes- ting methods

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.)

PT-IPQ

  • NP EN 556-2000 Sterilization of medical devices Requirements for terminally sterilized medical devices to be labelled"Sterile"

Indonesia Standards

GB-REG

US-FCR

CEN - European Committee for Standardization

RO-ASRO

European Committee for Standardization (CEN)

VN-TCVN

Society of Automotive Engineers (SAE)

Standard Association of Australia (SAA)

Underwriters Laboratories (UL)

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

RU-GOST R

  • 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

Lithuanian Standards Office

  • LST EN 62366-2008 Medical devices - Application of usability engineering to medical devices (IEC 62366:2007)

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

GOSTR

  • GOST R 58976-2020 Medical devices. Software. Part 2. Validation of software for medical device quality systems

GOST

European Committee for Electrotechnical Standardization(CENELEC)

  • EN 62366-1:2015 Medical devices - Part 1: Application of usability engineering to medical devices

US-AAMI

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

Korean Agency for Technology and Standards (KATS)

  • KS C 1103-1990 Glossary of Terms Used in Medical Electrical Equipment (General Terms)

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

US-VA