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Database: 365,228(8 Aug 2026)

Sexual Heart Medicine

Sexual Heart Medicine, Total:214 items.

The international standard classification for "Sexual Heart Medicine" includes: Medical Sciences and health care facilities in general , Medical equipment , Implants for surgery, prosthetics and orthotics .

The Chinese standard classification for "Sexual Heart Medicine" includes: Computer application , Sanitation in general , Medical apparatus and devices in general , Orthopedic devices .


Group Standards of the People's Republic of China

  • T/JCCIA 004-2022 Specification for debugging network equipment in data centers in the medical industry
  • T/CACM 1224-2019 Clinical guidelines for diagnosis and treatment of internal diseases in TCM Ischemic Cardiomyopathy
  • T/GZBC 16.3-2020 Specification for construction of medical data center—Part 3:Scientific research data center
  • T/NAHIEM 56-2022 Construction Standards for Radiotherapy Centers of Medical Institutions
  • T/GXAS 709-2024 Technical specification for diagnosis and treatment of anaphylactic rhinitis in Chinese medicine and Zhuang Medicine
  • T/CACM 1232-2019 Clinical guidelines for diagnosis and treatment of internal diseases in TCM Acute Myocardial Infarction with PCI
  • T/CACM 1139-2018 Traditional Chinese medicine guidelines for the diagnosis and treatment of mental diseases- Dysthymia
  • T/GDWJ 020-2023 Service specification of medical nursing assistant in medical institution
  • T/GDMDMA 0012.2-2021 Medical equipment standardized management in hospital - Part 2:Operation and management of allocation center
  • T/CADERM 9301-2024 Specification for medical services in emergency centers
  • T/GDWJ 012-2022 Specification for construction of medical data center Part 2:Operational data reepository
  • T/GZBC 16.1-2019 Pecification for construction of medical data center Part 1 Clinical data center
  • T/WSJD 51-2024 Water hygiene requirements for disinfection supply centers of medical institutions
  • T/CIATCM 037-2019 Profiling framework and classification for Traditional Chinese medical care informatics standards development
  • T/CACM 1169-2019 Clinical guidelines for diagnosis and treatment of internal diseases in TCM gasp syndrome(Chronic obstructive pulmonary disease and right heart failure)
  • T/CACM 1273-2019 Clinical guidelines for diagnosis and treatment of internal diseases in TCM Acute myocardial infarction
  • T/NAHIEM 83-2023 Construction standards for proton and heavy ion centers in medical institutions
  • T/GDWJ 012.2-2022 Medical Data Center Construction Specification Part 2: Operational Data Center
  • T/CACM 1167-2016 Guideline for Clinical Diagnosis and Treatment of TCM Diabetes mellitus complicated with heart disease
  • T/CACM 1325-2019 Diagnosis and treatment guidelines of traditional Chinese medicine for stable angina pectoris of coronary heart disease

Anhui Provincial Standard of the People's Republic of China

  • DB34/T 4351-2022 General Hospital Rehabilitation Treatment Center Construction Specifications
  • DB34/T 4789-2024 Specifications for the construction of ovarian malignant tumor diagnosis and treatment centers in general hospitals

Jilin Provincial Standard of the People's Republic of China

  • DB22/T 3247-2021 Standardization of traditional Chinese medicine treatment for children with myocarditis

Jiangsu Provincial Standard of the People's Republic of China

  • DB32/T 4383-2022 Specification for the service of chronic disease management center of primary medical institutions

Sichuan Provincial Standard of the People's Republic of China

  • DB5104/T 51.8-2021 Specifications for the Construction of Safe and Comfortable Consumption Environment Part 8: Medical Institutions

国家食品药品监督管理局

  • YY/T 1474-2016 Medical devices-Application of risk management to medical devices
  • YY 0989.6-2016 Implants for surgery―Active implantable medical devices―Part 6: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia(including implantable defibrillators)

未注明发布机构

  • DIN EN ISO 21549-3 E:2012-07 Healthcare Informatics Patient Data on Healthcare Cards Part 3: Clinical Data Core Dataset (Draft)
  • DIN EN ISO 21549-3:2004 Medical informatics – patient data on cards in healthcare – Part 3: Clinical data – core data set

Taiwan Provincial Standard of the People's Republic of China

Beijing Provincial Standard of the People's Republic of China

Korean Agency for Technology and Standards (KATS)

British Standards Institution (BSI)

  • BS EN 45502-2-1:2004 Active implantable medical devices - Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
  • BS EN 45502-2-2:2008 Active implantable medical devices - Part 2-2:Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)
  • BS ISO 21426:2018 Tourism and related services. Medical spas. Service requirements
  • BS EN 62366-1:2015+A1:2020 Medical devices. Application of usability engineering to medical devices
  • BS EN 62366-1:2015 Medical devices. Application of usability engineering to medical devices
  • BS EN 62366:2008 Medical devices - Application of usability engineering to medical devices
  • PD ISO/TS 22077-2:2015 Health informatics. Medical waveform format. Electrocardiography
  • BS PD IEC/TR 62366-2:2016 Medical devices. Guidance on the application of usability engineering to medical devices
  • BS EN 60598-2-25:1995 Luminaires - Particular requirements - Luminaires for use in clinical areas of hospitals and health care buildings
  • BS PD ISO/TR 37137:2014 Cardiovascular biological evaluation of medical devices. Guidance for absorbable implants
  • PD ISO/TS 22077-3:2015 Health informatics. Medical waveform format. Long term electrocardiography
  • BS EN 60976:2007 Medical electrical equipment - Medical electron accelerators - Functional performance characteristics
  • BS EN 60976:2008 Medical electrical equipment - Medical electron accelerators - Functional performance characteristics
  • BS EN 60601-2-25:1996 Medical electrical equipment - Particular requirements for safety - Specification for electrocardiographs
  • BS EN 60601-2-25:1993 Medical electrical equipment. Particular requirements for safety. Specification for electrocardiographs
  • BS EN 60601-2-25:2015 Medical electrical equipment. Particular requirements for the basic safety and essential performance of electrocardiographs
  • BS DD ENV 13735:2001 Health informatics - Interoperability of patient connected medical devices
  • DD ENV 12610-1998 Medical informatics. Medical product identification
  • PD IEC/TR 60601-4-2:2016 Medical electrical equipment. Guidance and interpretation. Electromagnetic immunity: performance of medical electrical equipment and medical electrical systems
  • PD ISO/TS 22077-4:2019 Health informatics. Medical waveform format. Stress test electrocardiography
  • DD ENV 12052-1998 Medical informatics. Medical imaging communication (MEDICOM)
  • BS EN 60601-2-27:2014 Medical electrical equipment. Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment
  • BS DD ENV 12443:2001 Medical informatics - Healthcare information framework (HIF)
  • DD ENV 12017-1998 Medical informatics. Medical informatics vocabulary (MIVoc)

European Committee for Standardization (CEN)

  • EN 45502-2-1:2004 Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
  • CENELEC EN 62366-2008 Medical devices - Application of usability engineering to medical devices

German Institute for Standardization

  • DIN EN 45502-2-1:2004 Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers); German version EN 45502-2-1:2003
  • DIN EN 45502-2-2:2008 Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators); German version EN 45502-2-2:2008
  • DIN EN 62366:2008 Medical devices - Application of usability engineering to medical devices (IEC 62366:2007); German version EN 62366:2008
  • DIN EN 60601-2-25:2001 Medical electrical equipment - Part 2-25: Particular requirements for the safety of electrocardiographs (IEC 60601-2-25:1993 + A1:1999); German version EN 60601-2-25:1995 + A1:1999
  • DIN VDE 0753-2:1983 Rules relating to intracardiac applications of medical electrical equipment VDE Guide
  • DIN 57753-2:1983 Rules relating to intracardiac applications of medical electrical equipment [VDE Guide]
  • DIN 58133:2008-07 Medical compression hosiery

Institute of Electrical and Electronics Engineers (IEEE)

  • 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 P1073.1.3.10/D3.0-1999 IEEE Draft Standard for Medical Device Communications -- Medical Device Data Language (MDDL) Virtual Medical Device, Specialized -- Cardiac Output
  • 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)

SCC

  • CEI EN 45502-2-1:2005 Active implantable medical devices - Part 2: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
  • AENOR UNE-EN 45502-2-1:2005 Active implantable medical devices — Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
  • BS 1882:1966 Flexible tubing for medical use
  • DANSK DS/EN 45502-2-1:2004 Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (Cardiac pacemakers)
  • 11/30187773 DC BS ISO 28621. Medical spas using natural resources. Service requirements
  • NS-EN 45502-2-1:2003 Active implantable medical devices — Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
  • AAMI/IEC 62366:2007 Medical devices - Application of usability engineering to medical devices
  • DANSK DS/EN 62366:2008 Medical devices - Application of usability engineering to medical devices
  • CEI EN 62366:2008 Medical devices - Application of usability engineering to medical devices
  • AENOR UNE-EN 62366:2009 Medical devices - Application of usability engineering to medical devices
  • AENOR UNE-EN 62366/A1:2009 Medical devices - Application of usability engineering to medical devices
  • BS EN 62366:2008+A1:2015 Medical devices. Application of usability engineering to medical devices
  • CEI EN 62366/A1:2008 Medical devices - Application of usability engineering to medical devices
  • DANSK DS/EN 62366/A1:2008 Medical devices - Application of usability engineering to medical devices
  • UNE-CR 14060:2001 Medical device traceability.
  • AS 1094:1993 Medical equipment - Single-use syringes (sterile) for general medical use
  • 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
  • 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
  • DANSK DS/ISO/TS 22077-2:2015 Health informatics – Medical waveform format – Part 2: Electrocardiography
  • DANSK DS/EN 62366-1:2015 Medical devices - Part 1: Application of usability engineering to medical devices
  • BS PD ISO/TS 22077-4:2019 Health informatics. Medical waveform format-Stress test electrocardiography
  • DANSK DS/EN 62366-1/AC:2019 Medical devices – Part 1: Application of usability engineering to medical devices
  • DANSK DS/EN 62366-1/A1:2020 Medical devices – Part 1: Application of usability engineering to medical devices
  • CEI EN 62366-1:2016 Medical devices Part 1: Application of usability engineering to medical devices
  • MIL MIL-C-42068-1989 CHEST, MEDICAL INSTRUMENT AND SUPPLY SET
  • DANSK DS/EN 16844+A2:2019 Aesthetic medicine services – Non-surgical medical treatments
  • BS EN 60601-2.25:1996 Medical electrical equipment. Particular requirements for safety. Specification for electrocardiographs
  • CSA Z317.10-2009(R2014) Handling of waste materials in health care facilities and veterinary health care facilities
  • DANSK DS/EN 16844+A1:2018 Aesthetic medicine services – Non-surgical medical treatments

American National Standards Institute (ANSI)

  • 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
  • AAMI TIR18:2010 Guidance on electromagnetic compatibility of medical devices in healthcare facilities
  • ANSI/AAMI/IEC 62366:2007 Medical devices - Application of usability engineering to medical devices
  • ANSI/AAMI/ISO 14117:2012 Active implantable medical devices - Electromagnetic compatibility - EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices
  • ANSI/AAMI/IEC 62366/A1:2014 Medical devices - Application of usability engineering to medical devices - Amendment 1

Association Francaise de Normalisation

  • NF S99-401:1994 Dispositifs médicaux - Élastomère de silicone de qualité médicale
  • NF X30-507:2018 Packaging for medical waste - Medical waste - Cardboard box with inner bag for infectious medical waste
  • NF C74-054:2008 Medical devices - Application of usability engineering to medical devices.
  • NF C74-208/A1:2001 Medical electrical equipment - Medical electron accelerators - Functional performance characteristics.
  • NF EN 45502-2-1:2004 Active implantable medical devices - Part 2-1: special rules for active implantable medical devices intended to treat bradyarrhythmia (pacemakers)
  • NF EN IEC 62667:2018 Medical electrical devices - Light ion beam medical devices - Performance characteristics
  • NF S90-480:1987 MEDICO-SURGICAL EQUIPMENT. IMPLANTS FOR SURGERY. CARDIOVASCULAR IMPLANTS. CARDIAC VALVE PROSTHESES.
  • NF C74-305:1996 Medical electrical equipment. Part 2 : particular requirements for the safety of electrocardiographs.
  • NF C74-502-2-1*NF EN 45502-2-1:2004 Active implantable medical devices - Part 2-1 : particular requirements for active implantable medical devices intended to treat bradyarrhythmia (Cardiac pacemakers)
  • NF S99-210:1998 MEDICAL DEVICES. RISK ANALYSIS. (EUROPEAN STANDARD EN 1441).
  • NF EN 45502-2-2:2008 Dispositifs médicaux implantables actifs - Partie 2-2 : exigences particulières pour les dispositifs médicaux implantables actifs destinés au traitement des tachyarythmies (y compris les défibrillateurs implantables)
  • NF C74-054-1*NF EN 62366-1:2015 Medical devices - Part 1 : application of usability engineering to medical devices
  • NF S90-701:1988 MEDICO-SURGICAL EQUIPMENT. BIOCOMPATIBILITY OF MATERIALS AND MEDICAL DEVICES. METHODS FOR EXTRACTION.
  • 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 X30-506:2015 Medical care waste - Packaging for liquid and infectious medical care waste - Specifications and tests
  • NF EN 16844+A2:2019 Services en médecine esthétique - Traitements médicaux, non chirurgicaux
  • NF EN IEC 60336:2021 Appareils électromédicaux - Gaines équipées pour diagnostic médical - Dimensions des foyers et caractéristiques connexes
  • NF EN 16844/IN2:2019 Services en médecine esthétique - Traitements médicaux, non chirurgicaux

ES-UNE

  • UNE-ISO 21426:2019 Tourism and related services. Medical spas. Service requirements.
  • 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 Medical devices - Part 1: Application of usability engineering to medical devices (Endorsed by AENOR in June of 2015.)
  • 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-EN IEC 62563-2:2021 Medical electrical equipment - Medical image display systems - Part 2: Acceptance and constancy tests for medical image displays (Endorsed by Asociación Española de Normalización in February of 2022.)

European Committee for Electrotechnical Standardization(CENELEC)

  • EN 45502-2-1:2003 Active implantable medical devices Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
  • EN 45502-2-2:2008 Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators) (Incorporating corrigendum April 2009)
  • EN 62366-1:2015 Medical devices - Part 1: Application of usability engineering to medical devices

International Electrotechnical Commission (IEC)

  • IEC 62366:2007/AMD1:2014 Medical devices - Application of usability engineering to medical devices
  • IEC 62366:2014 Medical devices - Application of usability engineering to medical devices
  • IEC 62366:2007+AMD1:2014 CSV Medical devices - Application of usability engineering to medical devices
  • IEC 62366-1:2015 Medical devices - Part 1: Application of usability engineering to medical devices
  • IEC TR 62366-2:2016 Medical devices - Part 2: Guidance on the application of usability engineering to medical devices
  • IEC 62366-1:2015/COR1:2016 Medical devices - Part 1: Application of usability engineering to medical devices
  • IEC 62366-1:2020 Medical devices - Part 1: Application of usability engineering to medical devices
  • IEC 62366-1:2015+AMD1:2020 CSV Medical devices - Part 1: Application of usability engineering to medical devices
  • IEC 60336:2005 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots

RU-GOST R

  • GOST 34244-2017 Telemedicine systems. General requirements for basic safety and essential performance of stationary telemedicine consultative and diagnostic centers
  • GOST R ISO 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 IEC 62366-2013 Medical devices. Application of usability engineering to medical devices
  • GOST R 50267.25-1994 Medical electrical equipment. Part 2. Particular requirements for safety of electrocardiographs
  • GOST R 57506-2017 Medical devices. Implantable defibrillators and other active implantable medical devices intended to treat tachyarrhythmia. Technical requirements for governmental purchases
  • GOST R 57298-2016 Radiopharmaceutical medicinal products. General requirements for organization of production of radiopharmaceuticals in medical organizations
  • GOST R 50267.27-1995 Medical electrical equipment. Part 2. Particular requirements for safety of electrocardiographic monitoring equipment
  • GOST ISO 10993-13-2016 Medical devices. Biological evaluation of medical devices. Part 13. Identification and quantification of degradation products from polymeric medical devices
  • GOST ISO 10993-11-2011 Medical devices. Biological evaluation of medical devices. Part 11. Tests for systemic toxicity

CN-CNCA

  • CNCA 08C-032-2001 Implementation Rules for Compulsory Certification of Medical Device Products ECG Machine
  • CNCA 08C-041-2001 Implementation Rules for Compulsory Certification of Medical Devices Artificial Heart-Lung Machine Heat Exchanger
  • CNCA 08C-035-2001 Implementation Rules for Compulsory Certification of Medical Device Products Hollow Fiber Dialyzer
  • CNCA 08C-042-2001 Implementation Rules for Compulsory Certification of Medical Devices Heat Exchange Water Tank for Artificial Heart-Lung Machine
  • CNCA 08C-043-2001 Implementation Rules for Compulsory Certification of Medical Devices Silicone Rubber Pump Tubes for Artificial Heart-Lung Machines
  • CNCA 08C-038-2001 Implementation Rules for Compulsory Certification of Medical Devices Artificial Heart-Lung Machine Roller Type Blood Pump
  • CNCA 08C-036-2001 Implementation Rules for Compulsory Certification of Medical Device Products Implantable Cardiac Pacemakers
  • CNCA 08C-040-2001 Implementation Rules for Compulsory Certification of Medical Devices Artificial Heart-Lung Machine Bubble Oxygenator
  • CNCA 08C-039-2001 Implementation Rules for Compulsory Certification of Medical Devices Artificial Heart-Lung Machine Rolling Type Pulsating Blood Pump

KR-KS

  • KS C 1929-2-2017(2022) U-healthcare ─ electrocardiograph ─ Particular requirements for the basic safety and performance
  • KS C IEC 60976-2020 Medical electrical equipment — Medical electron accelerators — Functional performance characteristics
  • KS P IEC 62366-1-2018 Medical devices — Part 1:Application of usability engineering to medical devices
  • KS P IEC 62366-1-2021 Medical devices — Part 1: Application of usability engineering to medical devices

Lithuanian Standards Office

  • LST EN 45502-2-1-2004 Active implantable medical devices -- Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
  • LST EN 62366-2008 Medical devices - Application of usability engineering to medical devices (IEC 62366:2007)
  • LST EN 45502-2-2-2008/AC-2009 Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)
  • LST EN 45502-2-2-2008 Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)

Danish Standards Foundation

  • DS/EN 45502-2-1:2004 Active implantable medical devices - Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (Cardiac pacemakers)
  • DS/EN 62366:2008 Medical devices - Application of usability engineering to medical devices
  • DS/EN 60336:2005 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots
  • DS/EN 45502-2-2:2008 Active implantable medical devices - Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)

AENOR

  • UNE-EN 45502-2-1:2005 Active implantable medical devices -- Part 2-1: Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers)
  • UNE-EN 62366:2009 Medical devices- Application of usability engineering to medical devices
  • UNE-EN 60336:2006 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots
  • UNE-EN 45502-2-2:2008 Active implantable medical devices -- Part 2-2: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators)
  • UNE 73703:1995 IN MINIMUM EQUIPMENT OF A FIRST STAGE MEDICAL CENTRE FOR THE TREATMENT OF THOSE INJURED OR CONTAMINED BY RADIOACTIVE ELEMENTS OR IONIZING RADIATION.

GSO

  • GSO IEC 62366:2014 Medical devices - Application of usability engineering to medical devices
  • OS GSO IEC 62366:2014 Medical devices - Application of usability engineering to medical devices
  • 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
  • OS GSO IEC 62366-1:2015 Medical devices - Part 1: Application of usability engineering to medical devices
  • GSO IEC 60336:2015 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots

International Organization for Standardization (ISO)

  • ISO/TR 37137:2014 Cardiovascular biological evaluation of medical devices - Guidance for absorbable implants
  • ISO/ASTM TR 52916:2022 Additive manufacturing for medical — Data — Optimized medical image data
  • IEC 62366:2007 Medical devices - Application of usability engineering to medical devices
  • ISO 14117:2012 Active implantable medical devices - Electromagnetic compatibility - EMC test protocols for implantable cardiac pacemakers, implantable cardioverter defibrillators and cardiac resynchronization devices
  • IEC/TR 62366-2:2016 Medical devices — Part 2: Guidance on the application of usability engineering to medical devices
  • IEC TR 62366-2-2016 Medical devices — Part 2: Guidance on the application of usability engineering to medical devices
  • IEC 62366:2007/AMD 1:2014 Medical devices — Application of usability engineering to medical devices — Amendment 1
  • ISO 14708-6:2010 Implants for surgery - Active implantable medical devices - Part 6: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (including implantable defibrillators)

GOST

CENELEC - European Committee for Electrotechnical Standardization

  • EN 62366:2008 Medical devices - Application of usability engineering to medical devices
  • PREN 50447-2004 Active implantable medical devices - Particular requirements for Heart-Lung Machines (HLM)

SE-SIS

  • SIS SS-IEC 976:1991 Medical electrical equipment — Medical electron accelerators — Functionalperformance charactetistics

Standard Association of Australia (SAA)

  • AS/NZS 4434.1:1996 Medical electrical equipment - Medical electron accelerators - Functional performance characteristics
  • AS/NZS 4434.2:1996 Medical electrical equipment - Medical electron accelerators - Periodic function performance testing

Canadian Standards Association (CSA)

ZA-SANS

  • SANS 10248-2:2009 Management of healthcare waste - Part 2: Management of healthcare risk waste for healthcare facilities and healthcare providers in rural and remote settings
  • SANS 60598-2-25:1994 Luminaires Part 2-25: Particular requirements - Luminaires for use in clinical areas of hospitals and health care buildings

American Society for Testing and Materials (ASTM)

  • ASTM F2761-09(2013) Medical Devices and Medical Systems - Essential safety requirements for equipment comprising the patient-centric integrated clinical environment (ICE) - Part 1: General requirements and conceptual model
  • ASTM F3211-17 Standard Guide for Fatigue-to-Fracture (FtF) Methodology for Cardiovascular Medical Devices

PL-PKN

Japanese Industrial Standards Committee (JISC)

  • JIS T 62366-1:2022 Medical devices -- Part 1: Application of usability engineering to medical devices
  • JIS Z 4120:2008 Medical electrical equipment -- X-ray tube assemblies for medical diagnosis -- Characteristics of focal spots

US-AAMI

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

CZ-CSN

NZ-SNZ

  • AS/NZS 2485:1995 Medical Equipment - Single-Use Winged Intravenous Devices (Sterile) for General Medical Use

BE-NBN

  • NBN C 74-336-1990 Characteristics of hospital hobs equipped with covers for medical diagnostics