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Database: 365,228(8 Aug 2026)

Medical device non-clinical

Medical device non-clinical, Total:83 items.

The international standard classification for "Medical device non-clinical" includes: Medical equipment in general .

The Chinese standard classification for "Medical device non-clinical" includes: Medical apparatus and devices in general .


Professional Standard - Medicine

Group Standards of the People's Republic of China

  • T/CACM 1138-2018 Traditional Chinese medicine guidelines for the diagnosis and treatment of mental diseases- Non-organic insomnia
  • T/CGCPU 026-2023 Design specifications for clinical trial protocol of cardiovascular interventional medical devices

国家药监局

  • YY/T 1754.1-2020 Preclinical animal study of medical devices—Part 1:General considerations

Standard Association of Australia (SAA)

RU-GOST R

GSO

  • OS GSO ISO 14155:2015 Clinical investigation of medical devices for human subjects -- Good clinical practice
  • GSO ISO 14155:2015 Clinical investigation of medical devices for human subjects -- Good clinical practice

SCC

  • BS EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects-Clinical investigation plans
  • ISO 14155:2020 Plus Redline Clinical investigation of medical devices for human subjects - Good clinical practice
  • DANSK DS/EN ISO 14155/AC:2011 Clinical investigation of medical devices for human subjects - Good clinical practice
  • AAMI/ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice
  • DANSK DS/ISO 14155:2020 Clinical investigation of medical devices for human subjects – Good clinical practice
  • 08/30116059 DC BS ISO 14155. Clinical investigation of medical devices for human subjects. Good clinical practice
  • BS EN 540:1993 Clinical investigation of medical devices for human subjects
  • NS-EN 540:1993 Clinical investigation of medical devices for human subjects
  • NS-EN ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
  • NS-EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
  • DANSK DS/EN ISO 14155:2020 Clinical investigation of medical devices for human subjects – Good clinical practice (ISO 14155:2020)
  • AENOR UNE-EN ISO 14155:2012 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
  • BS EN ISO 14155-1:2009 Clinical investigation of medical devices for human subjects-General requirements
  • DIN EN ISO 14155 E:2018 Draft Document - Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/DIS 14155:2018); German and English version prEN ISO 14155:2018
  • AAMI ST35:2003 Safe Handling and Biological Decontamination of Reusable Medical Devices in Health Care Facilities and in Nonclinical Settings
  • NS-EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans (ISO 14155-2:2003)
  • AAMI/ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (Includes Erratum, 2011)
  • DANSK DS/EN ISO 14155-1:2009 Clinical investigation of medical devices for human subjects - Part 1: General requirements
  • DANSK DS/EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans

European Committee for Standardization (CEN)

  • prEN 540-1992 Clinical investigation of medical devices for human subjects
  • EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
  • EN ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
  • EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
  • EN ISO 14155-2:2003 Clinical Investigation of Medical Devices for Human Subjects - Part 2: Clinical Investigation Plans ISO 14155-2:2003
  • EN 540:1993 Clinical Investigation of Medical Devices for Human Subjects Superseded by EN ISO 14155-1:2003

KR-KS

  • KS P ISO 14155-2022 Clinical investigation of medical devices for human subjects — Good clinical practice

Association Francaise de Normalisation

British Standards Institution (BSI)

  • BS EN 540:1993(1998) Clinicalinvestigationof medical devices for human subjects
  • 24/30467406 DC BS EN ISO 14155 Clinical investigation of medical devices for human subjects - Good clinical practice
  • BS EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects - Clinical investigation plans
  • 18/30344902 DC BS EN ISO 14155. Clinical investigation of medical devices for human subjects. Good clinical practice
  • BS EN ISO 14155:2011 Clinical investigation of medical devices for human subjects. Good clinical practice
  • BS EN ISO 14155:2020 Clinical investigation of medical devices for human subjects. Good clinical practice

Spanish Association for Standardization (UNE)

  • UNE-EN ISO 14155:2021 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
  • UNE-EN ISO 14155:2012 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
  • UNE-EN ISO 14155-2:2004 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans (ISO 14155-2:2003)

NL-NEN

  • NEN-EN 540-1994 Clinical investigation of medical devices for human subjects

German Institute for Standardization

  • DIN EN 540:1993 Clinical testing of medical devices on humans
  • DIN EN ISO 14155:2024 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/DIS 14155:2024); German and English version prEN ISO 14155:2024
  • DIN EN ISO 14155:2021-05 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020); German version EN ISO 14155:2020
  • DIN EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
  • DIN EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
  • DIN EN ISO 14155-2 E:2001-08 Clinical Studies of Medical Devices for Human Use Part 2: Clinical Study Protocol (Draft)
  • DIN EN ISO 14155:2021 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020); German version EN ISO 14155:2020
  • DIN EN 540 Berichtigung 1:1998 Clinical testing of medical devices on humans; German version EN 540: 1993

Danish Standards Foundation

  • DS/EN 540:1993 Clinical investigation of medical devices for human subjects
  • DS/EN ISO 14155:2013 Clinical investigation of medical devices for human subjects - Good clinical practice

Korean Agency for Technology and Standards (KATS)

  • KS P ISO 14155-2-2007(2012) Clinical investigation of medical devices for human subjects-Part 2:Clinical investigation plans
  • KS P ISO 14155-2-2019 Clinical investigation of medical devices for human subjects-Part 2:Clinical investigation plans
  • KS P ISO 14155-2:2007 Clinical investigation of medical devices for human subjects-Part 2:Clinical investigation plans
  • KS P ISO 14155-1-2007(2012) Clinical investigation of medical devices for human subjects-Part 1:General requirements
  • KS P ISO 14155-1-2019 Clinical investigation of medical devices for human subjects-Part 1:General requirements

International Organization for Standardization (ISO)

  • ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice
  • ISO 14155-2:2003 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plants
  • ISO 14155:2011/cor 1:2011 Clinical investigation of medical devices for human subjects - Good clinical practice; Technical Corrigendum 1
  • ISO 14155:1996 Clinical investigation of medical devices

GOST

IT-UNI

US-AAMI

  • ANSI/AAMI/ISO 14155:2020 Clinical investigation of medical devices for human subjects-Good clinical practice
  • ANSI/AAMI/ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice
  • AAMI TIR49-2013 Design of training and instructional materials for medical devices used in non-clinical environments

VN-TCVN

  • TCVN 7740-2-2007 Clinical investigation of medical devices for human subjects.Part 2: Clinical investigation plans

Lithuanian Standards Office

  • LST EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)

AT-ON

  • OENORM EN ISO 14155:2021 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)

PL-PKN

  • PN-EN ISO 14155-2021-02 E Clinical investigation of medical devices for human subjects -- Good clinical practice (ISO 14155:2020)

BE-NBN

  • NBN-EN 540-1993 Clinical investigation of medical devices for human subjects

American Society for Testing and Materials (ASTM)

  • ASTM D817-96(2004)e1 Standard Test Methods of Testing Cellulose Acetate Propionate and Cellulose Acetate Butyrate
  • ASTM D8179-18 Standard Guide for Characterizing Detergents for the Cleaning of Clinically-used Medical Devices

Institute of Electrical and Electronics Engineers (IEEE)