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iec in medicine

iec in medicine, Total:327 items.

In the international standard classification, iec in medicine involves: Vocabularies, Applications of information technology, Medical sciences and health care facilities in general, Laboratory medicine, Protection against crime, Microbiology, Terminology (principles and coordination), Medical equipment, Fluid storage devices, Burners. Boilers, Hospital equipment, Information sciences. Publishing, Radiation measurements, Quality, Radiation protection, Farming and forestry, Pharmaceutics, Ergonomics, Wastes, Dentistry, Air quality, Sterilization and disinfection, Education, Environmental protection, Photography, Analytical chemistry, Acoustics and acoustic measurements, Aircraft and space vehicles in general, Biology. Botany. Zoology, Electromagnetic compatibility (EMC), Optoelectronics. Laser equipment.


PH-BPS, iec in medicine

  • PNS ISO 19465:2021 Traditional Chinese medicine - Categories of traditional Chinese medicine (TCM) clinical terminological systems

KR-KS, iec in medicine

  • KS X ISO TS 16277-1-2017 Health informatics ― Categorial structures of clinical findings in traditional medicine ― Part 1: Traditional Chinese, Japanese and Korean medicine
  • KS X ISO TR 24291-2023 Health informatics Applications of machine learning technologies in imaging and other medical applications
  • KS P ISO 10993-18-2021 Biological evaluation of medical devices —Part 18: Chemical characterization of medical device materials within a risk management process
  • KS C IEC 61676-2017 Medical electrical equipment — Dosimetric instruments used for noninvasive measurement of X-ray tube voltage in diagnostic radiology
  • KS C IEC 61676-2017(2022) Medical electrical equipment — Dosimetric instruments used for noninvasive measurement of X-ray tube voltage in diagnostic radiology
  • KS X ISO HL7 27931-2016 Health informatics — Data exchange standards — Health level seven version 2.5 — An application protocol for electronic data exchange in healthcare environments

European Committee for Standardization (CEN), iec in medicine

  • DD ENV 12623-1997 Medical Informatics - Media Interchange in Medical Imaging Communications (MI-MEDICOM)
  • EN ISO 22367:2020 Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)
  • DD ENV 12967-1-1998 Medical Informatics - Healthcare Information System Architecture (HISA) - Part 1: Healthcare Middleware Layer
  • EN ISO 10993-18:2020/prA1 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
  • CEN ISO/TR 12296:2013 Ergonomics - Manual handling of people in the healthcare sector
  • EN ISP 10612-3:1996 Information Technology - International Standardized Profile RD - Relaying the MAC Service Using Transparent Bridging - Part 3: Token Ring LAN Subnetwork-Dependent, Media-Dependent Requirements ISO/IEC ISP 10612-3: 1995
  • EN ISO 10993-18:2020/A1:2023 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/Amd 1:2022)

British Standards Institution (BSI), iec in medicine

  • PD ISO/TS 16277-1:2015 Health informatics. Categorial structures of clinical findings in traditional medicine. Traditional Chinese, Japanese and Korean medicine
  • BS EN ISO 22367:2020 Medical laboratories. Application of risk management to medical laboratories
  • 19/30391662 DC BS ISO 22367. Medical laboratories. Application of risk management to medical laboratories
  • BS PD ISO/TS 18790-1:2015 Health informatics. Profiling framework and classification for Traditional Medicine informatics standards development. Traditional Chinese Medicine
  • BS PD ISO/TS 17948:2014 Health informatics. Traditional Chinese medicine literature metadata
  • DD ENV 12537-1:1998 Medical informatics. Registration of information objects used for EDI in healthcare.. The register
  • BS ISO 18665:2015 Traditional Chinese medicine. Herbal decoction apparatus
  • BS PD ISO/TS 16277-1:2015 Health informatics. Categorial structures of clinical findings in traditional medicine. Traditional Chinese, Japanese and Korean medicine
  • PD ISO/TS 17948:2014 Health informatics. Traditional Chinese medicine literature metadata
  • 19/30378891 DC BS EN IEC 62563-2. Medical electrical equipment. Medical image display systems. Part 2. Acceptance and constancy tests for medical image displays
  • ISO 10993-18:2020/Amd.1:2022 Biological evaluation of medical devices - Chemical characterization of medical device materials within a risk management process
  • BS EN ISO 10993-18:2020+A1:2023 Biological evaluation of medical devices - Chemical characterization of medical device materials within a risk management process
  • 18/30359002 DC BS IEC 62366-1 AMD1. Medical devices. Part 1. Application of usability engineering to medical devices
  • DD ENV 13609-2:2000 Healthcare informatics. Messages for maintenance of supporting information in healthcare systems. Updating of medical laboratory-specific information
  • BS PD ISO/TS 17938:2014 Health informatics. Semantic network framework of traditional Chinese medicine language system
  • PD ISO/TS 18790-1:2015 Health informatics. Profiling framework and classification for Traditional Medicine informatics standards development. Traditional Chinese Medicine
  • BS ISO 17217-1:2014 Traditional Chinese medicine. Ginseng seeds and seedlings. Panax ginseng C.A. Meyer
  • PD ISO/TS 17938:2014 Health informatics. Semantic network framework of traditional Chinese medicine language system
  • 18/30358832 DC BS EN ISO 10993-18. Biological evaluation of medical devices. Part 18. Chemical characterization of medical device materials within a risk management process
  • 21/30439273 DC BS EN ISO 10993-18 AMD1. Biological evaluation of medical devices - Part 18. Chemical characterization of medical device materials within a risk management process
  • BS EN ISO 12894:2001 Ergonomics of the thermal environment - Medical supervision of individuals exposed to extreme hot or cold environments
  • BS PD CEN ISO/TR 22411:2021 Ergonomics data for use in the application of ISO/IEC Guide 71:2014
  • BS EN 14485:2004 Health informatics - Guidance for handling personal health data in international applications in the context of the EU data protection directive
  • PD ISO/TS 5118:2022 Health informatics. Categorial structure of representation for evaluation of clinical practice guidelines of traditional Chinese medicine
  • PD ISO/TS 5346:2022 Health Informatics. Categorial structure for representation of Traditional Chinese Medicine clinical decision support system
  • BS EN 14484:2004 Health informatics - International transfer of personal health data covered by the EU data protection directive - High level security policy
  • BS DD ENV 13609-2:2000 Healthcare informatics - Messages for maintenance of supporting information in healthcare systems - Updating of medical laboratory-specific information
  • 22/30426016 DC BS ISO/IEC 3532-2. Information technology. 3D Printing and scanning. Medical image-Based modelling - Part 2: Segmentation
  • PD ISO/TR 19231:2014 Health informatics. Survey of mHealth projects in low and middle income countries (LMIC)
  • PD ISO/TR 15499:2016 Tracked Changes. Biological evaluation of medical devices. Guidance on the conduct of biological evaluation within a risk management process
  • 21/30426013 DC BS EN ISO/IEC 3532-1. Information technology. 3D Printing and scanning. Medical image-based modelling. Part 1. General requirement
  • PD ISO/TS 9491-1:2023 Biotechnology. Predictive computational models in personalized medicine research. Constructing, verifying and validating models
  • 20/30397190 DC BS IEC 61223-3-8. Evaluation and routine testing in medical imaging departments. Acceptance and constancy tests - Radiography and radioscopy
  • BS PD ISO/TR 80001-2-7:2015 Application of risk management for IT-networks incorporating medical devices. Application guidance. Guidance for Healthcare Delivery Organizations (HDOs) on how to self-assess their conformance with IEC 80001-1
  • BS PD IEC/TR 60601-4-3:2015 Medical electrical equipment. Guidance and interpretation. Considerations of unaddressed safety aspects in the third edition of IEC 60601-1 and proposals for new requirements
  • 23/30474286 DC BS EN IEC 60050-880. International Electrotechnical Vocabulary (IEV) - Part 880. Electrical equipment, electrical systems and software used in healthcare
  • 21/30377065 DC BS ISO 19461-2. Radiological protection. Measurement for the clearance of waste contaminated with radioisotopes for medical application - Part 2. Management of solid radioactive waste in nuclear medicine facilities
  • 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 14476:2005 Chemical disinfectants and antiseptics - Virucidal quantitative suspension test for chemical disinfectants and antiseptics used in human medicine - Test method and requirements (phase 2, step 1)
  • 14/30267012 DC BS ISO 17583. Health informatics. Terminology constraints for coded data elements expressed in ISO Harmonized Data Types used in healthcare information interchange
  • 17/30344601 DC BS EN ISO 10993-1. Biological evaluation of medical devices. Part 1. Evaluation and testing within a risk management process
  • BS PD IEC/TR 80001-2-8:2016 Application of risk management for IT-networks incorporating medical devices. Application guidance. Guidance on standards for establishing the security capabilities identified in IEC TR 80001-2-2
  • BS EN 14476:2013 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of virucidal activity in the medical area. Test method and requirements (Phase 2/Step 1)
  • BS EN 14476:2013+A2:2019 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of virucidal activity in the medical area. Test method and requirements (Phase 2/Step 1)
  • 23/30434159 DC BS EN IEC 62359. Ultrasonics. Field characterization. Test methods for the determination of thermal and mechanical indices and acoustic intensities related to medical diagnostic ultrasonic fields
  • BS EN ISO 11737-2:2010 Sterilization of medical devices. Microbiological methods. Tests of sterility performed in the definition, validation and maintenance of a sterilization process
  • BS EN ISO 11737-2:2020 Sterilization of medical devices. Microbiological methods. Tests of sterility performed in the definition, validation and maintenance of a sterilization process
  • BS EN ISO 11737-2:2009 Sterilization of medical devices - Microbiological methods - Tests of sterility performed in the definition, validation and maintenance of a sterilization process
  • 20/30429792 DC BS EN 61676. Medical electrical equipment. Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology

International Organization for Standardization (ISO), iec in medicine

  • ISO 19465:2017 Traditional Chinese medicine - Categories of traditional Chinese medicine (TCM) clinical terminological systems
  • ISO 22367:2020 Medical laboratories — Application of risk management to medical laboratories
  • IWA 35-2020 Quality of learning environments for students in healthcare professions - Requirements for healthcare education providers in care settings
  • ISO/TS 22990:2019 Traditional Chinese medicine — Categories of clinical terminological system to support the integration of clinical terms from traditional Chinese medicine and Western medicine
  • ISO/TS 17948:2014 Health informatics - Traditional Chinese medicine literature metadata
  • ISO 18665:2015 Traditional Chinese medicine - Herbal decoction apparatus
  • ISO/TS 18790-1:2015 Health informatics - Profiling framework and classification for Traditional Medicine informatics standards development - Part 1: Traditional Chinese Medicine
  • ISO/TS 16277-1:2015 Health informatics - Categorial structures of clinical findings in traditional medicine - Part 1: Traditional Chinese, Japanese and Korean medicine
  • ISO 18666:2015 Traditional Chinese medicine - General requirements of moxibustion devices
  • ISO/TR 24291:2021 Health informatics - Applications of machine learning technologies in imaging and other medical applications
  • ISO/TS 17938:2014 Health informatics - Semantic network framework of traditional Chinese medicine language system
  • ISO 17217-1:2014 Traditional Chinese medicine - Ginseng seeds and seedlings - Part 1: Panax ginseng C.A. Meyer
  • ISO/TR 12296:2012 Ergonomics - Manual handling of people in the healthcare sector
  • ISO/TR 15499:2016 Biological evaluation of medical devices - Guidance on the conduct of biological evaluation within a risk management process
  • ISO/CD TS 9321:2023 Health informatics — General requirements of multi-center medical data collaborative analysis
  • ISO/TR 22411:2021 Ergonomics data for use in the application of ISO/IEC Guide 71:2014
  • ISO/TS 5346:2022 Health informatics — Categorial structure for representation of traditional Chinese medicine clinical decision support system
  • IWA 35:2020 Quality of learning environments for students in healthcare professions — Requirements for healthcare education providers in care settings
  • ISO 10993-18:2020 Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management process — Amendment 1: Determination of the uncertainty factor
  • ISO 19610:2017 Traditional Chinese medicine - General requirements for industrial manufacturing process of red ginseng (Panax ginseng C.A. Meyer)
  • ISO/TS 21726:2019 Biological evaluation of medical devices — Application of the threshold of toxicological concern (TTC) for assessing biocompatibility of medical device constituents
  • ISO/CD 10993-1:2011 Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process
  • ISO 10993-1:2009/Cor 11:2010 Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process
  • ISO 11737-2:1998 Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the validation of a sterilization process
  • ISO/CD 22287 Health informatics — Workforce roles and capabilities for terminology and terminology services in healthcare (term workforce)
  • ISO/DTS 9491-1 Biotechnology — Predictive computational models in personalized medicine research — Part 1: Constructing, verifying and validating models
  • ISO/TS 9491-1:2023 Biotechnology — Predictive computational models in personalized medicine research — Part 1: Constructing, verifying and validating models
  • ISO/TS 22287:2019 Health informatics — Workforce roles and capabilities for terminology and terminology services in healthcare (term workforce)

Association Francaise de Normalisation, iec in medicine

  • NF S92-081*NF EN ISO 22367:2020 Medical laboratories - Application of risk management to medical laboratories
  • NF EN ISO 10637:2018 Médecine bucco-dentaire - Systèmes d'aspiration centrale
  • NF EN 1614:2006 Informatique de santé - Représentation des différentes sortes de propriété dédiée dans la médecine de laboratoire
  • NF EN ISO 20749:2018 Médecine bucco-dentaire - Amalgame dentaire en capsules prédosées
  • NF S99-501-18*NF EN ISO 10993-18:2020 Biological evaluation of medical devices - Part 18 : chemical characterization of medical device materials within a risk management process
  • NF EN ISO 10993-18:2020 Évaluation biologique des dispositifs médicaux - Partie 18 : caractérisation chimique des matériaux des dispositifs médicaux au sein d'un processus de gestion du risque
  • NF EN ISO 12381:2019 Informatique de santé - Expressions relatives au temps explicites utilisées dans le domaine de la santé
  • NF X35-210*NF EN ISO 12894:2001 Ergonomics of the thermal environment - Medical supervision of individuals exposed to extreme hot or cold environments
  • NF EN ISO 16954:2015 Médecine bucco-dentaire - Méthodes d'essai pour le traitement du biofilm dans les conduites d'eau de l'unit dentaire
  • NF EN ISO 10993-18/A1:2023 Évaluation biologique des dispositifs médicaux - Partie 18 : caractérisation chimique des matériaux des dispositifs médicaux au sein d\'un processus de gestion du risque - Amendement 1 : détermination du coefficient d\'incertitude
  • NF EN ISO 10993-1:2020 Évaluation biologique des dispositifs médicaux - Partie 1 : évaluation et essais au sein d'un processus de gestion du risque
  • NF ISO 18385:2016 Réduire au maximum le risque de contamination de l'ADN dans les produits utilisés pour recueillir, stocker et analyser du matériel biologique en criminalistique - Exigences
  • NF EN ISO 12894:2001 Ergonomie des ambiances thermiques - Surveillance médicale des personnes exposées à la chaleur ou au froid extrêmes
  • NF ISO 19461-2:2022 Radioprotection - Mesurage pour la libération des déchets contaminés par des radioisotopes lors des applications médicales - Partie 2 : Gestion des déchets radioactifs solides dans les installations de médecine nucléaire
  • NF EN 61676/A1:2009 Appareils électromédicaux - Instruments de dosimétrie pour la mesure non invasive de la tension du tube radiogène dans la radiologie de diagnostic
  • NF T72-185:2007 Chemical disinfectants and antiseptics - Virucidal quantitative suspension test for chemical disinfectants and antiseptics used in human medicine - Test method and requirements (phase 2, step 1).
  • NF T72-185/IN1:2007 Chemical disinfectants and antiseptics - Virucidal quantitative suspension test for chemical disinfectants and antiseptics used in human medicine - Test method and requirements (phase 2, step 1).
  • NF S97-702-2:2013 Health informatics - Individual case safety reports (ICSRs) in pharmacovigilance - Part 2: human parmaceutical reporting requirements for ICSR
  • NF S97-554-1*NF EN 13609-1:2005 Health Informatics - Messages for maintenance of supporting information in healthcare systems - Part 1 : updating of coding schemes
  • NF EN IEC 61676:2023 Appareils électromédicaux - Appareils de dosimétrie pour le mesurage non invasif de la tension du tube radiogène dans la radiologie de diagnostic
  • FD ISO/TR 22710:2019 Médecine bucco-dentaire - Vocabulaire de la chaîne de procédé, de la TAO dentaire à la CFAO, pour restaurations prothétiques implantaires - Planification amont dans la chaîne de procédé numérique

AENOR, iec in medicine

  • UNE-ENV 12388:1997 MEDICAL INFORMATICS. ALGORITHM FOR DIGITAL SIGNATURE SERVICES IN HEALTH CARE.
  • UNE-EN 1614:2007 Health informatics - Representation of dedicated kinds of property in laboratory medicine
  • UNE-EN 62464-1:2007 Magnetic resonance equipment for medical imaging -- Part 1: Determination of essential image quality parameters (IEC 62464-1:2007).
  • UNE-EN 61676:2003/A1:2009 Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology
  • UNE-EN 61676:2003 Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology
  • UNE-EN ISO 10993-1:2010 Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)

Group Standards of the People's Republic of China, iec in medicine

  • T/CSRS CSRS-2022 Guidelines for the Construction of Sleep Medicine Centers in China
  • T/HARACM 0007-2023 TCM medical record evaluation tool based on evidence-based medicine PICO model
  • T/CMAM A10-2021 Chinese Association of Ethnic Medicine Yao Medicine Terminology Standards
  • T/CIATCM 039-2019 Functional specification of the management information system for education in the hospitals of Traditional Chinese Medicine
  • T/ACSC 01-2022 Standard for the construction of assisted reproductive medicine centers
  • T/CARDTCM CARDTCM006-2022 TCM True Qi Movement Health Care Teaching Standards
  • T/CNMIA 0017-2020 Evaluation of the ability of independent medical imaging centers run by society
  • T/BPMA 0007.2-2020 Guidelines for the management of medical observation of close contacts of coronavirus disease 2019 cases part 2: centralized medical observation????
  • T/CACM 1358-2021 Guidelines for prevention and control of myopia with traditional Chinese medicine to children and adolescents (for students and parents)
  • T/CHSA 001-2020 Consensus of Chinese oral medicine experts on maintaining periodontal health (first edition)
  • T/CSBME 038-2021 Quality control of image and diagnostic report in regional remote medical imaging center
  • T/CHAS 20-3-5-2022 Pharmacy administration and Pharmacy practice in Healthcare institutions—— Part 3-5: Pharmaceutical supply services——Pharmacy intravenous admixture

German Institute for Standardization, iec in medicine

  • DIN EN ISO 22367:2020 Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)
  • DIN 58959-3:2014 Medical microbiology - Quality management in medical microbiology - Part 3: Requirements for request and report forms
  • DIN EN 62563-1/A1:2016 Medical electrical equipment - Medical image display systems - Part 1: Evaluation methods (IEC 62B/983/CDV:2015); German and English version EN 62563-1:2010/FprA1:2015
  • DIN EN 1614:2006-12 Health informatics - Representation of dedicated kinds of property in laboratory medicine; English version EN 1614:2006
  • DIN 58959-17:2011 Medical microbiology - Quality management in medical microbiology - Part 17: Requirements for the use of control strains for the examination of mycobacteria; Text in German and English
  • DIN 58959-6 Beiblatt 1:2019-06 Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing; Supplement 1: Recommended test organisms for frequently used culture media; Text in German and Eng...
  • DIN 58959-6:2019-06 Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing
  • DIN EN 62563-1:2014 Medical electrical equipment - Medical image display systems - Part 1: Evaluation methods (IEC 62563-1:2009); German version EN 62563-1:2010
  • DIN EN ISO 10993-18:2021-03 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020); German version EN ISO 10993-18:2020 / Note: To be amended by DIN EN ISO 10993-18/A1 (2021-10).
  • DIN EN ISO 10993-18:2023-11 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020 + Amd 1:2022); German version EN ISO 10993-18:2020 + A1:2023
  • DIN EN IEC 62464-1:2021 Magnetic resonance equipment for medical imaging - Part 1: Determination of essential image quality parameters (IEC 62462-1:2018); German version EN IEC 62464-1:2019
  • DIN EN IEC 62464-1:2021-10 Magnetic resonance equipment for medical imaging - Part 1: Determination of essential image quality parameters (IEC 62462-1:2018); German version EN IEC 62464-1:2019
  • DIN EN 62366-1:2017 Medical devices - Part 1: Application of usability engineering to medical devices (IEC 62366-1:2015 + COR1:2016); German version EN 62366-1:2015 + AC:2015
  • DIN EN 61691-3-2:2002-11 Behavioural languages - Part 3-2: Mathematical operation in VHDL (IEC 61691-3-2:2001); German version EN 61691-3-2:2001
  • DIN 58969-10:2003 Medical microbiology - Diagnostics of infectious diseases in serological and molecular biology - Part 10: Complement fixation test (CFT)
  • DIN EN 60731/A1:2015 Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy (IEC 62C/596A/CDV:2014); German and English version EN 60731:2012/FprA1:2014
  • DIN 6855-11:2016-08 Constancy testing of nuclear medicine instruments - Part 11: Radionuclide calibrators (IEC/TR 61948-4:2006, modified)
  • DIN 58959-6 Beiblatt 1:2019 Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing; Supplement 1: Recommended test organisms for frequently used culture media; Text in German and Englis
  • DIN EN ISO 10993-18:2021 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020); German version EN ISO 10993-18:2020
  • DIN EN ISO 10993-18/A1:2021-10 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/DAM 1:2021); German and English version...
  • DIN EN 62464-1:2019 Magnetic resonance equipment for medical imaging - Part 1: Determination of essential image quality parameters (IEC 62B/1068/CDV:2017); German and English version prEN 62464-1:2017
  • DIN 6862-1:1992-12 Identification and characterisation of radiological images in medical diagnosis; direct and indirect radiography
  • DIN 6862-3:2021 Identification and characterization of radiological images in medical diagnosis - Part 3: Patient orientation in image generating procedures
  • DIN 6862-3:2021-06 Identification and characterization of radiological images in medical diagnosis - Part 3: Patient orientation in image generating procedures
  • DIN 6855-11:2009 Constancy testing of nuclear medicine instruments - Part 11: Radionuclide calibrators (IEC/TR 61948-4:2006, modified)
  • DIN 6855-11:2016 Constancy testing of nuclear medicine instruments - Part 11: Radionuclide calibrators (IEC/TR 61948-4:2006, modified)
  • DIN 6814-6:2009-05 Terms in the field of radiological technique - Part 6: Diagnostic use of X-radiation in medicine
  • DIN V ENV 13609-2:2000 Health informatics - Messages for maintenance of supporting information in healthcare systems - Part 2: Updating of medical laboratory-specific information; English version ENV 13609-2:2000
  • DIN 58959-6 Beiblatt 2:2022 Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing; Supplement 2: Recommended test organisms for frequently used testing reagents, dyes and biological ma
  • DIN 58959-6 Beiblatt 2:2021 Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing; Supplement 2: Recommended test organisms for frequently used testing reagents, dyes and biological ma
  • DIN 58959-6 Beiblatt 2:2022-07 Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing; Supplement 2: Recommended test organisms for frequently used testing reagents, dyes and biological...
  • DIN EN ISO 10993-1:2021-05 Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-10); German version EN ISO 10993-1:2020
  • DIN EN 60601-1-11:2021 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 60601-1-8:2021 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
  • DIN 6868-150:2013 Image quality assurance in diagnostic X-ray departments - Part 150: RöV acceptance test of medical radiographic and fluoroscopic X-ray equipment
  • DIN EN 62464-2:2011 Magnetic resonance equipment for medical imaging - Part 2: Classification criteria for pulse sequences (IEC 62464-2:2010); German version EN 62464-2:2011
  • DIN EN 61157:2013 Standard means for the reporting of the acoustic output of medical diagnostic ultrasonic equipment (IEC 61157:2007 + A1:2013); German version EN 61157:2007 + A1:2013
  • DIN 58967-20:2003 Medical microbiology and immunology - Diagnostics of infectious diseases and diseases of the immune system in serology and molecular biology - Part 20: General method-specific requirements for immunofluorescence tests (IFT)
  • DIN 6855-1:2009 Constancy testing of nuclear medical measuring systems - Part 1: Radiation counting systems for measurements in vivo and in vitro (IEC/TR 61948-1:2001, modified)
  • DIN EN 61223-3-4:2001-10 Evaluation and routine testing in medical imaging departments - Part 3-4: Acceptance tests; Imaging performance of dental X-ray equipment (IEC 61223-3-4:2000); German version EN 61223-3-4:2000
  • DIN EN 61676:2010-05 Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology (IEC 61676:2002+A1:2008); German version EN 61676:2002+A1:2009 / Note: To be replaced by DIN EN IEC 61676 (2022-05).
  • DIN EN IEC 61676:2022-05 Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology (IEC/CDV 61676:2021); German and English version prEN IEC 61676:2022 / Note: Date of issue 2022-03-25*Intended as repl...
  • DIN EN IEC 61207-2:2021 Expression of performance of gas analyzers - Part 2: Measuring oxygen in gas utilizing high-temperature electrochemical sensors (IEC 61207-2:2019); German version EN IEC 61207-2:2019
  • DIN EN IEC 61265:2018 Electroacoustics - Instruments for measurement of aircraft noise - Performance requirements for systems to measure sound pressure levels in noise certification of aircraft (IEC 61265:2018); German version EN IEC 61265:2018
  • DIN EN 61676:2010 Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology (IEC 61676:2002+A1:2008); German version EN 61676:2002+A1:2009
  • DIN 6856-1:2007 Radiological film viewing boxes and viewing conditions - Part 1: Requirements and measures of quality assurance in medical diagnostics
  • DIN EN ISO 10993-1:2017 Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO/DIS 10993-1:2017); German and English version prEN ISO 10993-1:2017
  • DIN 58942-4 Beiblatt 1:2004-01 Medical microbiology - Culture media - Part 4: Transport systems for specimens containing bacteria - Systems, media and conditions for the transport of selected pathogens in clinical specimens
  • DIN EN 55011:2011 Industrial, scientific and medical equipment - Radio-frequency disturbance characteristics - Limits and methods of measurement (IEC/CISPR 11:2009, modified + A1:2010); German version EN 55011:2009 + A1:2010
  • DIN EN IEC 61223-3-8:2023 Evaluation and routine testing in medical imaging departments - Part 3-8: Acceptance and constancy tests - Radiography and radioscopy (IEC/CDV 61223-3-8:2022); German and English version prEN IEC 61223-3-8:2022
  • DIN EN IEC 61674:2023-03 Medical electrical equipment - Dosimeters with ionization chambers and/or semiconductor detectors as used in X-ray diagnostic imaging (IEC/CDV 61674:2023); German and English version prEN IEC 61674:2023 / Note: Date of issue 2023-02-17*Intended as repl...
  • DIN 58942-4 Beiblatt 1:2004 Medical microbiology - Culture media - Part 4: Transport systems for specimens containing bacteria - Systems, media and conditions for the transport of selected pathogens in clinical specimens
  • DIN 58942-4 Bb.1:2004 Medical microbiology - Culture media - Part 4: Transport systems for specimens containing bacteria - Systems, media and conditions for the transport of selected pathogens in clinical specimens
  • DIN EN 13609-1:2005-09 Health Informatics - Messages for maintenance of supporting information in healthcare systems - Part 1: Updating of coding schemes; English version EN 13609-1:2005
  • DIN EN IEC 60746-4:2019-10 Expression of performance of electrochemical analyzers - Part 4: Dissolved oxygen in water measured by membrane-covered amperometric sensors (IEC 60746-4:2018); German version EN IEC 60746-4:2019 / Note: DIN IEC 60746-4 (1996-07) remains valid alongsid...

Professional Standard - Public Safety Standards, iec in medicine

Lithuanian Standards Office , iec in medicine

  • LST EN 62366-2008 Medical devices - Application of usability engineering to medical devices (IEC 62366:2007)
  • LST EN 1614-2007 Health informatics - Representation of dedicated kinds of property in laboratory medicine
  • LST EN 62563-1-2010 Medical electrical equipment - Medical image display systems -- Part 1: Evaluation methods (IEC 62563-1:2009)
  • LST EN 61676-2004 Medical electrical equipment. Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology (IEC 61676:2002)
  • LST EN 61676-2004/A1-2009 Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology (IEC 61676:2002/A1:2008)
  • LST L ENV 13609-2-2002 Health informatics - Messages for maintenance of supporting information in healthcare systems - Part 2: Updating of medical laboratory-specific information
  • LST EN 62464-2-2011 Magnetic resonance equipment for medical imaging -- Part 2: Classification criteria for pulse sequences (IEC 62464-2:2010)
  • LST EN 60731-2012 Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy (IEC 60731:2011)
  • LST EN 61691-3-2-2003 Behavioural languages. Part 3-2: Mathematical operation in VHDL (IEC 61691-3-2:2001)
  • LST EN 62464-1-2007 Magnetic resonance equipment for medical imaging - Part 1: Determination of essential image quality parameters (IEC 62464-1:2007)
  • LST EN 61223-2-4-2001 Evaluation and routine testing in medical imaging departments. Part 2-4: Constancy tests. Hard copy cameras (IEC 61223-2-4:1994)
  • LST EN 60601-1-11-2010 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 606
  • LST EN 60601-1-8-2007/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 (IEC
  • LST EN 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 6060
  • LST EN 60601-1-11/A1-2021 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
  • LST EN 60601-1-8-2007 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
  • LST EN 60601-1-8-2007/AC-2010 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
  • LST EN 60601-1-8/A2-2021 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
  • LST EN 61223-2-5-2001 Evaluation and routine testing in medical imaging departments. Part 2-5: Constancy tests. Image display devices (IEC 61223-2-5:1994)

Korean Agency for Technology and Standards (KATS), iec in medicine

  • KS X ISO TS 16277-1:2017 Health informatics ― Categorial structures of clinical findings in traditional medicine ― Part 1: Traditional Chinese, Japanese and Korean medicine
  • KS X ISO TS 16277-1-2017(2022) Health informatics ― Categorial structures of clinical findings in traditional medicine ― Part 1: Traditional Chinese, Japanese and Korean medicine
  • KS P ISO 10993-18:2021 Biological evaluation of medical devices —Part 18: Chemical characterization of medical device materials within a risk management process
  • KS C IEC 61676:2017 Medical electrical equipment — Dosimetric instruments used for noninvasive measurement of X-ray tube voltage in diagnostic radiology
  • 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 C CISPR 28-2002 Industrial, scientific and medical equipment(ISM)-Guidelines for emission levels within the bands designated by the ITU

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

  • GB/T 40670-2021 Guidelines for establishment and development of traditional Chinese medical thesauri
  • GB/T 38327-2019 Health informatics—Classification of traditional Chinese medicine data sets
  • GB/T 38324-2019 Health informatics—Semantic network framework of traditional Chinese medicine language system
  • GB/T 16886.1-2022 Biological evaluation of medical devices—Part 1: Evaluation and testing within a risk management process

Danish Standards Foundation, iec in medicine

  • DS/EN 1614:2007 Health informatics - Representation of dedicated kinds of property in laboratory medicine
  • DS/ENV 12537-1:1997 Medical informatics - Registration of information objects used for EDI in healthcare - Part 1: The Register
  • DS/ISO/TR 24291:2021 Health informatics – Applications of machine learning technologies in imaging and other medical applications
  • DS/ENV 13609-2:2000 Health informatics - Messages for maintenance of supporting information in healthcare systems - Part 2: Updating of medical laboratory-specific information
  • DS/EN 61676:2003 Medical electrical equipment - Dosimetric instuments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology
  • DS/EN 61676/A1:2009 Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology
  • DS/ISO 10993-1:2020 Biological evaluation of medical devices – Part 1: Evaluation and testing within a risk management process (ISO/FDIS 10993-1:2018)

CN-STDBOOK, iec in medicine

  • 图书 3-9704 2018-2019 Collection of Group Standards of the Chinese Geriatrics Society

American National Standards Institute (ANSI), iec in medicine

  • ANSI N13.54-2008 Fetal Radiation Dose Calculations in Nuclear Medicine
  • BS EN IEC 61676:2023 Medical electrical equipment. Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology (British Standard)

US-MSFC, iec in medicine

Hebei Provincial Standard of the People's Republic of China, iec in medicine

RU-GOST R, iec in medicine

  • GOST R 52960-2008 Forensic science laboratories accreditation. Guidance on the application of GOST R ISO/IEC 17025
  • GOST R IEC 61676-2006 Medical electrical equipment. Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology
  • GOST R 53133.4-2008 Medical laboratory technologies. Quality control of clinical laboratory tests. Part 4. Rules for conducting of clinical audit of efficiency of laboratory provision of medical institution activity
  • GOST R ISO/IEC 29109-1-2012 Information technology. Biometrics. Conformance testing methodology for biometric data interchange formats defined in ISO/IEC 19794. Part 1. Generalized conformance testing methodology

Canadian Standards Association (CSA), iec in medicine

  • CSA Z314.23-2012 Stérilisation par agent chimique des dispositifs médicaux réutilisables dans les établissements de santé (première édition)
  • CSA ISO 22367:2021 Medical laboratories - Application of risk management to medical laboratories (Adopted ISO 22367:2020, first edition, 2020-02)
  • CSA IEC-CISPR 11:04-CAN/CSA:2004 Industrial, scientific and medical (ISM) radio-frequency equipment Electromagnetic disturbance characteristics Limits and methods of measurement First Edition; IEC CISPR 11:2003

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, iec in medicine

  • GB/T 42467.2-2023 Clinical Terminology of Traditional Chinese Medicine Part 2: Surgery
  • GB/T 42467.6-2023 TCM Clinical Terminology Part 6: Gynecology
  • GB/T 42467.1-2023 Clinical Terminology of Traditional Chinese Medicine Part 1: Internal Medicine
  • GB/T 42467.7-2023 TCM Clinical Terminology Part 7: Pediatrics
  • GB/T 42467.8-2023 TCM Clinical Terminology Part 8: Ophthalmology
  • GB/T 42467.3-2023 TCM Clinical Terminology Part 3: Dermatology
  • GB/T 42467.5-2023 Clinical Terminology of Traditional Chinese Medicine Part 5: Orthopedics and Traumatology
  • GB/T 42467.4-2023 TCM Clinical Terminology Part 4: Anorectal Science
  • GB/T 16886.18-2022 Biological evaluation of medical devices—Part 18: Chemical characterization of medical device materials within a risk management process
  • GB 16361-1996 Radiological protection standards for the patient in clinical nuclear medicine
  • GB/T 42467.9-2023 TCM Clinical Terminology Part 9: Otolaryngology
  • GB/T 42410-2023 Characteristic description framework of traditional Chinese medicine information standard in health informatics
  • GB/T 16886.1-2011 Biological evaluation of medical devices.Part 1: Evaluation and testing within a risk management process
  • GB/T 21415-2008 In vitro diagnostic medical devices.Measurement of quantities in biological samples.Metrological traceability of values assigned to calibrators and control materials

国家卫生计生委, iec in medicine

  • WS/T 544-2017 Medical digital imaging Chinese packaging and communication specifications
  • WS/T 548-2017 Digital Imaging Communications in Medicine (DICOM) Chinese Standard Compliance Test Specification

Zhejiang Provincial Standard of the People's Republic of China, iec in medicine

  • DB3305/T 140-2020 Guidelines for the management of centralized isolation and medical observation of new coronary pneumonia

Liaoning Provincial Standard of the People's Republic of China, iec in medicine

  • DB21/T 3838-2023 Hygienic Management Standards for Centralized Isolation Medical Observation Sites

IT-UNI, iec in medicine

  • UNI EN ISO 10993-18:2021 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process
  • UNI EN ISO 10993-1:2021 Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process

未注明发布机构, iec in medicine

  • BS EN ISO 10993-18:2020 Biological evaluation of medical devices Part 18 : Chemical characterization of medical device materials within a risk management process
  • BS EN ISO 10993-1:2020 Tracked Changes. Biological evaluation of medical devices. Evaluation and testing within a risk management process

ES-UNE, iec in medicine

  • UNE-EN ISO 10993-18:2021 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
  • UNE-EN ISO 10993-1:2021 Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-10)
  • UNE-EN 61676:2003 ERRATUM Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology.
  • UNE-EN IEC 61676:2023 Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology (Endorsed by Asociación Española de Normalización in June of 2023.)

AT-OVE/ON, iec in medicine

  • OVE EN 62366-1-2021 Medical devices - Part 1: Application of usability engineering to medical devices ( IEC 62366-1:2015) (german version)
  • OVE EN IEC 55011 (Fragment 1):2021 Industrial, scientific and medical equipment - Radio-frequency disturbance characteristics - Limits and methods of measurement - Requirements for air-gap wireless power transfer (WPT) (IEC CIS/B/763/CDV) (english version)
  • OVE EN IEC 61207-2:2021 Expression of performance of gas analyzers - Part 2: Measuring oxygen in gas utilizing high-temperature electrochemical sensors (( IEC 61207-2:2019) EN IEC 61207-2:2019) (german version)

American Society for Testing and Materials (ASTM), iec in medicine

  • ASTM F2900-11 Standard Guide for Characterization of Hydrogels used in Regenerative Medicine
  • ASTM E1647-16 Standard Practice for Determining Contrast Sensitivity in Radiology

Professional Standard - Environmental Protection, iec in medicine

  • HJ 228-2021 Technical Specifications for Centralized Treatment Engineering of Chemical Disinfection of Medical Waste
  • HJ/T 228-2006 Technical specifications for chemical disinfection centralized treatment engineering on medical waste (on trial)
  • HJ/T 228-2005 Technical specifications for chemical disinfection centralized treatment engineering on medical waste (on trial)

VE-FONDONORMA, iec in medicine

AT-ON, iec in medicine

  • OENORM EN ISO 10993-18:2021 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
  • OENORM EN ISO 10993-18/A1:2021 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020/DAM 1:2021) (Amendment)

CH-SNV, iec in medicine

  • SN EN ISO 10993-18:2020 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)

PL-PKN, iec in medicine

  • PN-EN ISO 10993-18-2020-11 E Biological evaluation of medical devices -- Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)

US-CLSI, iec in medicine

  • CLSI C51-A-2012 Expression of Measurement Uncertainty in Laboratory Medicine; Approved Guideline

国家食品药品监督管理局, iec in medicine

  • YY/T 1512-2017 Implementation Guidelines for Biological Evaluation in the Risk Management Process of Biological Evaluation of Medical Devices
  • YY/T 0722-2016 Medical electrical equipment Dosimetric instruments for non-accessible measurement of X-ray tube voltage in diagnostic radiology

TH-TISI, iec in medicine

  • TIS 2395.13-2008 Biological evaluation of medical devices.part 13: identification and quantification of degradation products from polymeric medical devices

American Nuclear Society (ANS), iec in medicine

  • ANS 3.4-1996 Medical Certification and Monitoring of Personnel Requiring Operator Licenses for Nuclear Power Plants

NATO - North Atlantic Treaty Organization, iec in medicine

  • STANAG 3497-2010 AEROMEDICAL TRAINING OF AIRCREW IN AIRCREW CBRN EQUIPMENT AND PROCEDURES (ED 3; To obtain please contact your national Defense Standardization Office or the NATO Standardization Office website: http:/ so.nato.int so@ Phone: +32 (0)2 – 707 5556@ email: nso
  • STANAG 2873-1982 Concept of Operations of Medical Support in Nuclear@ Biological and Chemical Environments - AMedP-7(A) (ED 2 AMD 0; To obtain please contact your national Defense Standardization Office or the NATO Standardization Office website: http:/ so.nato.int so@ Ph
  • STANAG 2873-1996 Concept of Operations of Medical Support in Nuclear@ Biological and Chemical Environments - AMedP-7(C) (ED 3 AMD 0; To obtain please contact your national Defense Standardization Office or the NATO Standardization Office website: http:/ so.nato.int so@ Ph
  • STANAG 3497-1988 Aeromedical Training of Aircrew in Aircrew NBC Equipment and Procedures (ED 1 AMD 3; To obtain please contact your national Defense Standardization Office or the NATO Standardization Office website: http:/ so.nato.int so@ Phone: +32 (0)2 – 707 5556@ email
  • AAMEDP-1.8-2018 AEROMEDICAL TRAINING OF AIRCREW IN AIRCREW CBRN EQUIPMENT AND PROCEDURES (ED A@ Ver. 1)

Tianjin Provincial Standard of the People's Republic of China, iec in medicine

  • DB12/T 1072-2021 Disinfection technical guidelines for centralized isolation medical observation points for respiratory infectious diseases

US-AAMI, iec in medicine

  • ANSI/AAMI/ISO TIR15499:2012 Biological evaluation of medical devices - Guideance on the conduct of biological evaluation within a risk management process
  • AAMI TIR49-2013 Design of training and instructional materials for medical devices used in non-clinical environments

Institute of Electrical and Electronics Engineers (IEEE), iec in medicine

North Atlantic Treaty Organization Military Agency for Standardization (NATO-MAS), iec in medicine

  • STANAG 2879-2021 MEDICAL ASPECTS IN THE MANAGEMENT OF A MAJOR INCIDENT/MASS CASUALTY SITUATION - AMedP-1.10 EDITION B

North Atlantic Treaty Organization Standards Agency, iec in medicine

  • STANAG 2873-2007 CONCEPT OF OPERATIONS OF MEDICAL SUPPORT IN CHEMICAL, BIOLOGICAL, RADIOLOGICAL, AND NUCLEAR ENVIRONMENTS - AMedP-7(D)
  • STANAG 3497-1994 AEROMEDICAL TRAINING OF AIRCREW IN AIRCREW NBC EQUIPMENT AND PROCEDURES

Jiangsu Provincial Standard of the People's Republic of China, iec in medicine

  • DB3202/T 1012-2021 Work Specifications for Centralized Medical Observation Sites for Prevention and Control of Novel Coronavirus Pneumonia Epidemic
  • DB32/T 3758-2020 Disinfection technical specifications for centralized medical observation places for the prevention and control of novel coronavirus pneumonia

Professional Standard - Hygiene , iec in medicine

  • WS/T 253-2005 In vitro diagnostic medical devices Measurement of quantities in samples of biological origin Description of reference materials
  • WS/T 254-2005 In vitro diagnostic medical devices Measurement of quantities in samples of biological origin Presentation of reference measurement procedures

Professional Standard - Medicine, iec in medicine

  • YY/T 0722-2009 Medical electrical equipment.Dosimetric instrument used for non-invasive measurement of X-ray tube voltage in diagostic radiology
  • YY/T 0722-2016/tec 61676-2009 Medical electrical equipment Dosimetry instruments for non-intrusive measurement of X-ray tube voltage in diagnostic radiology
  • YY/T 0722-2016/tec 61676:2009
  • YY/T 0638-2008 In vitro diagnostic medical devices.Measurement of quantities in biological samples.Metrological traceability of assigned values for catalytic concentration of enzymes in calibrators and control materials

International Electrotechnical Commission (IEC), iec in medicine

  • IEC 61676:2002+AMD1:2008 CSV Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology
  • IEC 61676:2023 RLV Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology
  • IEC 61676:2023 Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology
  • IEC 103/74/PAS:2008 IEC/PAS 62593: Measurement method of a half-wavelength voltage for mach-zehnder optical modulator in wireless communication and broadcasting systems

Japanese Industrial Standards Committee (JISC), iec in medicine

  • JIS T 0993-1:2012 Biological evaluation of medical devices -- Part 1: Evaluation and testing within a risk management process

IEEE - The Institute of Electrical and Electronics Engineers@ Inc., iec in medicine

  • IEEE 802.15.4N AMD 1-2016 Low-Rate Wireless Networks Amendment 1: Physical Layer Utilizing China Medical Bands (IEEE Computer Society)

European Committee for Electrotechnical Standardization(CENELEC), iec in medicine

  • EN 60598-2-25:1994 Luminaires - Part 2-25: Particular requirements - Luminaires for use in clinical areas of hospitals and health care buildings (Incorporates Amendment A1: 2004)
  • EN IEC 61676:2023 Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology

IAEA - International Atomic Energy Agency, iec in medicine

  • WS-G-2.7-2005 Management of Waste from the Use of Radioactive Material in Medicine@ Industry@ Agriculture@ Research and Education

ITU-T - International Telecommunication Union/ITU Telcommunication Sector, iec in medicine

  • ITU-T K.133-2018 Electromagnetic environment of body-worn equipment in the 2.4 GHz and 13.56 MHz industrial@ scientific and medical band (Study Group 5)

Beijing Provincial Standard of the People's Republic of China, iec in medicine

  • DB11/T 1749.2-2020 Disinfection Technical Specifications for Epidemic Prevention and Control of Respiratory Infectious Diseases Part 2: Centralized Isolation Medical Observation Places

Shanxi Provincial Standard of the People's Republic of China, iec in medicine

  • DB14/T 1984.3-2020 Disinfection Technical Guidelines for Prevention and Control of Novel Coronavirus Pneumonia Epidemic Part 3: Centralized Medical Observation Sites

PT-IPQ, iec in medicine

  • NP EN 1174-3-2000 Sterilization of medical devices Estimation of the population of micro-organisms on product Part 3:Guide to the methods for validation of microbiological techniques




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