40 years of medical

40 years of medical, Total:493 items.

The international standard classification for "40 years of medical" includes: Medical Sciences and health care facilities in general , Medical equipment in general , Finances. Banking. Monetary systems. Insurance , Medical equipment .

The Chinese standard classification for "40 years of medical" includes: Standardization and quality management , Medical apparatus and devices in general , Finance and Insurance , Medical science , Public medical equipment .

Jiangxi Provincial Standard of the People's Republic of China

DB36/T 1981-2024 Service management specifications for outpatient services for the elderly in medical institutions
DB36/T 1980-2024 Construction specifications for elderly-friendly medical institutions

Group Standards of the People's Republic of China

T/CHAS 10-3-7-2023 Quality and safety management of Chinese hospital—— Part 3-7: Medical service support —— Medical Information
T/SDAS 475-2022 Chinese medicine rehabilitation diagnosis guide for children and adolescents with idiopathic scoliosis
T/CMAM Z1-Z9-2019 Tibetan medical technical operation specification
T/FNASS 09-2021 Standards for medical care services for the elderly in elderly care institutions
T/CAS 842-2024 Evaluation of quality management maturity of medical equipment in medical institutions
T/CMAM D1-D5-2019 Dai medical technical operation specification
T/GDWJ 020-2023 Service specification of medical nursing assistant in medical institution
T/CIATCM 048-2019 Functional specification of basic medical management information system in Traditional Chinese Medicine section in primary medical and health care institution
T/LEECH 001-2019 Standard treatment of Hirudotheropy of Chinese acupuncture
T/CMAM M10-20-2019 Mongolian medical technical operation specification
T/TIC 017-2024 Systematic dental medicine
T/CIATCM 094-2020 Data interface technical specification in Traditional Chinese Medicine section in primary medical and health care institution
T/GZYYJHH 0001-2023 "Internet +" medical care combined with geriatric medicine diagnosis and treatment service standards
T/CACM 1220-2019 Clinical guidelines for diagnosis and treatment of internal diseases in TCM Frailty in older adults
T/CACM 1134-2018 Traditional Chinese medicine guidelines for the diagnosis and treatment of mental diseases- Senile mental disorder
T/CRACM 0011-2023 Combined Chinese Medicine Therapy for Myopia in Children and Adolescents
T/CACM 1580-2024 Guidelines for diagnosis and treatment of senile osteoporosis with the integrated traditional Chinese and western medicine
T/CHAS 10-3-4-2019 Quality and safety management of Chinese hospital—Part 3-4: Medical service support —Medical device
T/CAGR 013-2024 Traditional Chinese medicine therapy in sanatorium General introduction
T/CIATCM 049-2019 Basic datasets for the health Information of basic medical care information system in Traditional Chinese Medicine section in primary medical and health care institution

Ningxia Provincial Standard of the People's Republic of China

DB64/T 1986-2024 Standards for evaluation of the construction of age-friendly medical institutions

Beijing Provincial Standard of the People's Republic of China

DB11/T 1964-2022 Technical specifications for the assessment of elderly-friendly medical institutions

National Health Commission of the People's Republic of China

WS/T 803-2022 Service standards for medical nursing assistants of older adults in home and community

Heilongjiang Provincial Standard of the People's Republic of China

DB23/T 2785-2020 Medical institutions provide green channel service specifications for the elderly to seek medical treatment

Jilin Provincial Standard of the People's Republic of China

DB22/T 3115-2020 Standards for diagnosis and treatment of traditional Chinese medicine in the elderly with mild cognitive impairment
DB22/T 3557-2023 Standards for TCM diagnosis and treatment of functional dyspepsia in the elderly accompanied by anxiety and depression
DB22/T 3358-2022 Medical management norms for square cabin hospitals
DB22/T 3437-2023 TCM diagnosis and treatment norms for functional dyspepsia in the elderly

Professional Standard - Agriculture

40兽药质量标准汇编(2006至2011年)-2012 Imported veterinary drug standard iodine-glycerin mixed solution
40兽药质量标准汇编(2012年)-2013 Domestic Veterinary Medicine Spider Fragrance Powder
40兽药质量标准2017年版 Volume I of Chemical Drugs Quality Standards for Veterinary Drugs Sihua Paamidophos Solution

Zhejiang Provincial Standard of the People's Republic of China

DB33/T 2568-2023 Medical Security Management and Service Standards for Designated Medical Institutions
DB3311/T 237-2023 Technical specifications for artificial breeding of horsemouth

Tianjin Provincial Standard of the People's Republic of China

DB12/ 597-2015 Regulations on Medical Waste Treatment in Medical and Health Institutions

Taiwan Provincial Standard of the People's Republic of China

CNS 6282-1980 Medical Dressing Forceps
CNS 5941-1980 Tuning Forks (for Medical Use)
CNS 6286-1980 Medical Hooks
CNS 7329-1981 Adhesive Tape, Medical
CNS 6283-1980 Medical Forceps
CNS 6628-1989 Finger Sack for Medical Use

Jiangsu Provincial Standard of the People's Republic of China

DB32/T 3761.40-2021 Part 40 of the Technical Specifications for the Prevention and Control of the Novel Coronavirus Pneumonia Epidemic: COVID-19 Medical Waste Management
DB3212/T 1065-2021 Standards for Quality Evaluation of Medical Devices Used in Medical Institutions
DB32/T 4553-2023 Guidelines of adverse events monitoring for hospital medical device

Professional Standard - Medicine

YY/T 0316-2008 Medical devices - Application of risk management to medical devices
YY/T 0316-2016 Medical devices-Application of risk management to medical devices
YY/T 0316-2003 Medical devices -- Application of risk management to medical devices

Shandong Provincial Standard of the People's Republic of China

DB37/T 4236-2020 Newly added medical insurance agreement designated medical institution management specifications
DB37/T 4379-2021 Standard for medical security service of designated medical institution

Chongqing Provincial Standard of the People's Republic of China

DB50/T 1556.2-2024 Rating of service levels for health care workers Part 2: Caregivers for elderly patients

未注明发布机构

DIN EN ISO 14971 E:2018-08 Application of medical device risk management in medical devices (draft)
DIN 13119 E:2008-09 Medical instruments bowel scissors
DIN 96056 E:2015-09 Medical instruments - Bone raspatory
DIN 96056:2016-03 Medical instruments - Bone raspatory
ANSI/AAMI/ISO 14971:2019 Medical devices— Application of risk management to medical devices
DIN EN ISO 14971:2001 Medical devices - Application of risk management to medical devices
DIN EN IEC 62127-1 E:2022-04 Ultrasonics - Hydrophones - Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz
IEC 80601-2-77:2023 Medical electrical equipment
DIN 96056 E:2022-08 Medical instruments - Bone raspatory
DIN 58852 E:2020-06 Medical instruments - Probes
DIN EN ISO 14971:2022 Medical devices – applying risk management to medical devices
ANSI/AAMI/ISO 15225:2016 Medical devices—Quality management—Medical device nomenclature data structure
CAN/CSA-ISO 17664:2018 Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices
DIN 58852 E:2014-02 Medical instruments - Probes
DIN 96056:2023-03 Medical instruments - Bone raspatory

Liaoning Provincial Standard of the People's Republic of China

DB21/T 3683-2022 Regulations on Hygienic Management of Medical Waste in Medical and Health Institutions

国家卫生计生委

WS/T 527-2016 Names of general medical sites

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

GB/T 42062-2022 Medical devices—Application of risk management to medical devices
GB/Z 42217-2022 Medical device —Validation of software for medical device quality system

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

GJB 4574-1990*GJBz 20032-1990 Service ship medical cabin layout and installation of medical equipment
GJB 162-1986 Surface ship medical cabin layout and installation of medical equipment

国家食品药品监督管理局

YY/T 1474-2016 Medical devices－Application of risk management to medical devices

Professional Standard - Hygiene

WS 307-2009 Standard of symbols for medical institutions

国家药监局

YY/T 0802-2020 Processing of medical devices—Information to be provided by the medical device manufacturer

IMO - International Maritime Organization

TA114E-2001 Medical First Aid (2000 Edition; Course + Compendium)

Institute of Electrical and Electronics Engineers (IEEE)

NFPA (Fire) 99 Health Care Facilities Code, 2021 Edition
NFPA (Fire) 1999 Protective Clothing for Emergency Medical Operations, 2018 Edition
NFPA (Fire) 450 Guide for Emergency Medical Services and Systems, 2021 Edition
NFPA (Fire) 1582 Standard on Comprehensive Occupational Medical Program for Fire Departments, 2022 Edition
IEEE P1073.1.3.11/D3.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Capnometer
IEEE P1073.1.3.7/D4.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Blood Pressure
IEEE P1073.1.3.6/D6.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - ECG
IEEE P1073.1.3.8/D4.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Temperature
IEEE Std 11073-10207-2017 IEEE Health informatics--Point-of-care medical device communication Part 10207: Domain Information and Service Model for Service-Oriented Point-of-Care Medical Device Communication
IEEE 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 P1073.1.3.5/D04:2000 Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Defibrillator Device
IEEE P1073.1.3.9/D3.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Airway Flow
IEEE Std P1073.1.3.8/D4.0 IEEE Draft Standard for Medical Device Communications -- Medical Device Data Language (MDDL) Virtual Medical Device, Specialized -- Temperature
P1073.1.3.4/D3.0 IEEE Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Medical Device Specializations - Pulse Oximeter
IEEE P1073.1.3.4/D3.0 IEEE Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Medical Device Specializations - Pulse Oximeter

NZ-SNZ

AS/NZS 2696:1996 Medical Devices - Polymer Urethral Catheters for General Medical Use (Amendment 1 March 1999)
NZS 4304:2002 Management of Healthcare Waste

SCC

CAN/CSA Z314-2023 Canadian medical device reprocessing in all health care settings, Includes Update No. 1 (2024)
ASTM PS101-97 Guide on security framework for Healthcare Information (Withdrawn 2000)
ASTM F340-71(1993) Specification for Pilot-Type Medical Countersinks (Withdrawn 1997)
ASTM PS102-97 Guide for Internet and Intranet Healthcare Security (Withdrawn 2000)
CAN/CSA-ISO 14971-2001 Medical Devices - Application of Risk Management to Medical Devices (Adopted ISO 14971:2000, first edition, 2000-12-15)
MIL MIL-DTL-3476/13C-1997 BRASSARD, MEDICAL SERVICE, VETERINARY CORPS (SUPERSEDING MIL-B-3476/13B DATED MAY 10, 1992)
MIL MIL-C-42068-1989 CHEST, MEDICAL INSTRUMENT AND SUPPLY SET
ASTM PS100-97 Specification for Authentication of Healthcare Information Using Digital Signatures (Withdrawn 2000)
DANSK DS/EN 16844+A2:2019 Aesthetic medicine services – Non-surgical medical treatments
AAMI/ISO 15223-2000 Medical devices -- Symbols to be used with medical device labels, labelling and information to be supplied - Includes Amendment 1, dated September 24, 2001
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
DANSK DS/EN 62127-1/A1:2007 Ultrasonics – Hydrophones – Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz
CEI EN 62127-1/A1:2008 Ultrasonics - Hydrophones Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz
CEI EN 62127-1:2008 Ultrasonics - Hydrophones Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz
DANSK DS/EN 62127-1:2007 Ultrasonics – Hydrophones – Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz
NS-ENV 12612:1997 Medical informatics — Messages for the exchange of healthcare administrative information
NS 683:1980 Medical test tubes
CAN/HSO 83001:2018 Telehealth
BS DD ENV 12967-1:1998 Medical informatics. Healthcare Information System Architecture (HISA)-Healthcare middleware layer
CAN/CSA-C22.2 No.60601-2-40-2001(C2014) Medical electrical devices - Part 2-40: Special safety requirements for electromyographs and evoked potential devices
UL Subject 1637-2017 Standard for Home Health Care Signaling Equipment (CSDS Proposal, 3/17/2017)
CSA ISO 17664-2:2023 Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 2: Non-critical medical devices
AAMI/ISO 17664-2:2022 Processing of health care products—Information to be provided by the medical device manufacturer for the processing of medical devices—Part 2: Non-critical medical devices
DANSK DS/ISO 17664-2:2021 Processing of health care products – Information to be provided by the medical device manufacturer for the processing of medical devices – Part 2: Non-critical medical devices
CAN/CSA Z17664-2006(R2016) Sterilization of Medical Devices - Information to be Provided by the Manufacturer for the Processing of Resterilizable Medical Devices (Adopted ISO 17664:2004, first edition, 2004-03-01)
AAMI/ISO 17664-1:2022 Processing of health care products—Information to be provided by the medical device manufacturer for the processing of medical devices—Part 1: Critical and semi-critical medical devices
CAN/CSA-ISO 17664-2-2023 Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 2: Non-critical medical devices
AS 2786:1985 Symbols - Health care in hospitals
AS 3003:1976 Rules for electrical wiring and equipment in electromedical treatment areas of hospitals (known as the SAA code for electrical installations in electromedical treatment areas)
CAN/CSA-ISO 14971:2007(R2012) Medical Devices - Application of Risk Management to Medical Devices
DANSK DS/EN ISO 14971:2012 Medical devices – Application of risk management to medical devices
AS 2684:1984 Medical equipment - Humidifiers, for medical use
DANSK DS/ISO 17664-1:2021 Processing of health care products – Information to be provided by the medical device manufacturer for the processing of medical devices – Part 1: Critical and semi-critical medical devices
DIN V ENV 12967-1:1998 Medical informatics - Healthcare Information System Architecture (HISA) - Part 1: Healthcare Middleware Layer; English version ENV 12967-1:1998
CAN/CSA-ISO 14971:2007(C2012) Medical devices - Application of risk management to medical devices
CEI UNI EN ISO 14971:2020 Medical devices - Application of risk management to medical devices
AAMI/ISO 14971:2019 Medical devices - Application of risk management to medical devices
DANSK DS/ISO 14971:2020 Medical devices – Application of risk management to medical devices
CAN/CSA-ISO 14971:2001(R2006) Medical Devices - Application of Risk Management to Medical Devices
MIL MIL-DTL-3476/12C-1997 BRASSARD, MEDICAL SERVICE, GENEVA CONVENTION (SUPERSEDING MIL-B-3476/12B DATED MAY 10, 1992)
DANSK DS/EN ISO 17664-2:2024 Processing of health care products – Information to be provided by the medical device manufacturer for the processing of medical devices – Part 2: Non-critical medical devices (ISO 17664-2:2021)
AAMI/ISO 17664:2017 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices.
CEI 62-252:2017 Guide to managing medical IT software and networks in the healthcare context Part 2: Medical IT networks
BS EN ISO 14971:2019 Medical devices. Application of risk management to medical devices
CAN/CSA-ISO 14971:2001(C2006) Medical devices - Application of risk management to medical devices
CEI UNI EN ISO 15223-1:2018 Dispositivi medici - Simboli da utilizzare nelle etichette del dispositivo medico, nell'etichettatura e nelle informazioni che devono essere fornite Parte 1: Requisiti generali
BS PD CEN ISO/ASTM/TR 52916:2022 Additive manufacturing for medical. Data. Optimized medical imagedata
ISO 14971:2019 Plus Redline Medical devices - Application of risk management to medical devices
NS-EN ISO 17664-2:2023 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021)
DANSK DS/EN ISO 15225:2016 Medical devices – Quality management – Medical device nomenclature data structure
AAMI/ISO 15225:2016 Medical devices - Quality management - Medical device nomenclature data structure
CEI UNI EN/ISO 15225:2016 Medical devices - Quality management - Medical device nomenclature data structure
MIL MIL-DTL-11484/168D-2020 Lapel Button, Length of Service (20, 25, 30, 35, 40, 45, 50 and 55 Years), NASA
AAMI EQ93:2019 Medical equipment management - Vocabulary used in medical equipment programs
CSA Z314-2023 Reprocessing of medical devices in Canada in all healthcare settings
CAN/CSA-ISO 17664-1-2023 Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical 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
DANSK DS/EN 62366:2008 Medical devices - Application of usability engineering to medical devices
AAMI/ISO 15225:2010 Medical devices - Quality management - Medical device nomenclature data structure
AAMI/IEC 62366:2007 Medical devices - Application of usability engineering to medical devices
BS 3232:1960 Specification for safety requirements for medical treatment lamps
DANSK DS/EN 62366/A1:2008 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
MIL MIL-DTL-11484/168C-2015 Lapel Button, Length of Service (20, 25, 30, 35, 40, 45, 50 and 55 Years), NASA
DIN 58857:2019 Medical instruments - Directors
CSA C22.2 No.125-M1984-1984(R2004) Electromedical Equipment
NS 632:1980 Syringes for medical use
CSA C22.2 No.125-1979 Electromedical equipment
DIN 96056:2016 Medical instruments - Bone raspatory
BS PD ISO/TR 80002-2:2017 Medical device software-Validation of software for medical device quality systems
NS-EN ISO 17664-1:2021 Processing of health care products – Information to be provided by the medical device manufacturer for the processing of medical devices – Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)
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/EN ISO 17664-1:2021 Processing of health care products – Information to be provided by the medical device manufacturer for the processing of medical devices – Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)
BS 3232:1968 Specification for safety requirements for medical treatment lamps
CSA C22.2 No.125-1973 Electro-Medical Equipment
CSA Z314.23-16:2016 Chemical sterilization of reusable medical devices in healthcare settings
BS EN ISO 11197:2004 Medical supply units
AWWA JAW50186 Journal AWWA — Rehabilitation of 1940s Water Mains
CAN/CSA-Z305.8-2003(R2013) Medical Supply Units
DIN EN ISO 17664-2 E:2023 Draft Document - Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021); German and English version prEN ISO 176...
NS-EN 13824:2004 Sterilization of medical devices — Aseptic processing of liquid medical devices — Requirements
DANSK DS/ISO 11197:2019 Medical supply units
BS EN ISO 11197:2016 Medical supply units
BS 1882:1966 Flexible tubing for medical use
CAN/CSA Z305.8-2003(R2023) Medical Supply Units
SN-CR 14060:2000 Medical device traceability
CSA C22.2 No.125-M1984-1984(C2004) Electromedical equipment
CSA Z317.10-15:2016 Handling of healthcare waste

National Fire Protection Association (NFPA)

NFPA 99H PART 1-2002 NFPA 99, Health Care Facilities 2002 Edition, with Commentary
NFPA 1999-2007 Standard on Protective Clothing for Emergency Medical Operations 2008 Edition
NFPA 1582-2006 Standard on Comprehensive Occupational Medical Program for Fire Departments 2007 Edition
NFPA 99H CROSS-REFERENCE TABLE-2002 Cross-Reference Table for NFPA 99, Health Care Facilities, 2002-1999 Editions
NFPA 99-2021 Health Care Facilities Code (Effective Date: 8/31/2020)
NFPA 99 AMD 3-2012 Health Care Facilities Code Effective Date: 8/29/2012
NFPA 99-2015 Health Care Facilities Code (Effective Date: 9/3/2014)
NFPA 1500H PART 1 CH 8-1998 Medical and Physical
NFPA FPH SECTION 7-13-2003 Emergency Medical Services
NFPA FPH SECTION 13-8-2003 Healthcare Occupancies

ASHRAE - American Society of Heating@ Refrigerating and Air-Conditioning Engineers@ Inc.

ASHRAE DA-07-037-2007 A New Idea That Is 40 Years Old-Air Curtain Hospital Operating Room Systems
ASHRAE JOURN 40-9 GWR-1998 ASHRAE Journal (Volume 40 Number 9; September 1998)
ASHRAE JOURN 40-8 BFL-1998 ASHRAE Journal (Volume 40 Number 8; August 1998)
ASHRAE JOURN 40-2 PSNC-1998 ASHRAE Journal (Volume 40 Number 2; February 1998)
ASHRAE JOURN 40-6 WEW-1998 ASHRAE Journal (Volume 40 Number 6; June 1998)
ASHRAE JOURN 40-3 ATA-1998 ASHRAE Journal (Volume 40 Number 3; March 1998)
ASHRAE JOURN 40-4 VHL-1998 ASHRAE Journal (Volume 40 Number 4; April 1998)

U.S. Green Building Council

GBC LEED HC RATING SYSTEM-2010 LEED for Healthcare Rating System (Updated April 2012)

British Standards Institution (BSI)

BS EN 62127-1:2007+A1:2013 Ultrasonics. Hydrophones. Measurement and characterization of medical ultrasonic fields up to 40 MHz
BS EN 62127-1:2008 Ultrasonics. Hydrophones. Measurement and characterization of medical ultrasonic fields up to 40 MHz
DD ENV 12610-1998 Medical informatics. Medical product identification
DD ENV 12052-1998 Medical informatics. Medical imaging communication (MEDICOM)
BS DD ENV 12443:2001 Medical informatics - Healthcare information framework (HIF)
DD ENV 12017-1998 Medical informatics. Medical informatics vocabulary (MIVoc)
BS EN 62366-1:2015+A1:2020 Medical devices. Application of usability engineering to medical devices
BS EN ISO 14971:2009 Medical devices - Application of risk management to medical devices
BS EN ISO 14971:2007 Medical devices - Application of risk management to medical devices
BS EN 16224:2012 Healthcare provision by chiropractors
BS EN ISO 14971:2012 Medical devices. Application of risk management to medical devices
BS EN 62366-1:2015 Medical devices. Application of usability engineering to medical devices
21/30433049 DC BS EN 60601-2-40. Medical electrical equipment. Part 2-40. Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment
BS EN 62366:2008 Medical devices - Application of usability engineering to medical devices
DD ENV 12435-2000 Medical informatics. Expression of results of measurements in health sciences
BS EN ISO 14971:2001 Medical devices - Application of risk management to medical devices
BS EN 16224:2012+A1:2014 Healthcare provision by chiropractors
DD ENV 13607-2000 Health informatics. Messages for the exchange of information on medicine prescriptions
BS PD IEC/TR 62366-2:2016 Medical devices. Guidance on the application of usability engineering to medical devices
BS EN ISO 14971:2019+A11:2021 Medical devices - Application of risk management to medical devices
BS PD IEC/TR 60601-4-1:2017 Medical electrical equipment. Guidance and interpretation. Medical electrical equipment and medical electrical systems employing a degree of autonomy
BS EN 556-2:2004 Sterilization of medical devices. Requirements for medical devices to be designated "STERILE". Requirements for aseptically processed medical devices
BS EN ISO 15225:2010 Medical devices - Quality management - Medical device nomenclature data structure
BS EN 556-1:2024 Sterilization of medical devices. Requirements for medical devices to be designated "STERILE" - Requirements for terminally sterilized medical devices
DD ENV 12623-1998 Medical informatics. Media interchange in Medical imaging communications (MI-MEDICOM)
BS EN 556-2:2015 Sterilization of medical devices. Requirements for medical devices to be designated 'STERILE'. Requirements for aseptically processed medical devices
BS DD ENV 12611:1998 Medical informatics - Categorical structure of systems of concepts - Medical devices
BS EN ISO 15225:2016 Medical devices. Quality management. Medical device nomenclature data structure
DD ENV 12611-1998 Medical informatics. Categorical structure of systems of concepts. Medical devices
BS DD ENV 12612:1998 Medical informatics - Messages for the exchange of healthcare administrative information
PD ISO/TR 25555:2024 Ageing societies. Accessibility and usability considerations for home healthcare products, related services and environments
BS ISO 5741:2023 Healthcare organization management. Pandemic response. Temporary medical facility
BS PD CEN/TR 15640:2007 Health informatics — Measures for ensuring the patient safety of health software
BS DD CEN/TS 14463:2003 Health informatics - A syntax to represent the content of medical classification systems (CIaML)
PD IEC/TR 60601-4-2:2016 Medical electrical equipment. Guidance and interpretation. Electromagnetic immunity: performance of medical electrical equipment and medical electrical systems
BS EN ISO 11197:2019 Medical supply units
BS ISO 24163-2:2024 Clamp-in tyre valves for tyre pressure monitoring systems - Test methods and performance
BS ISO 17664-2:2021 Processing of health care products. Information to be provided by the medical device manufacturer for the processing of medical devices. Non-critical medical devices
BS EN 16686:2015 Osteopathic healthcare provision

American Society for Testing and Materials (ASTM)

ASTM F1146-91 Specification for Rotary Wing Specialized Medical Transport Units (Withdrawn 2000)
ASTM F1328-00 Standard Guide for Training Emergency Medical Technician (Basic) to Prepare Patients for Medical Transportation (Withdrawn 2006)
ASTM F1283-91 Specification for Fixed Wing Specialized Medical Transport Units (Withdrawn 2000)
ASTM F1187-91 Specification for Fixed Wing Specialized Medical Transport Units (Withdrawn 2000)
ASTM F604-94 Specification for Silicone Elastomers Used in Medical Applications (Withdrawn 2001)
ASTM F1118-91(2003) Standard Specification for National Air Medical Transport Units Resources Catalog (Withdrawn 2007)
ASTM F1230-89 Specification for Minimum Performance Requirements for Emergency Medical Service (EMS) Ground Vehicles (Withdrawn 1997)
ASTM F1258-95(2006) Standard Practice for Emergency Medical Dispatch

Canadian Standards Association (CSA)

CSA Z387-2013 Safe use of electrosurgical medical devices and systems in health care (First Edition; Errata: September 2013)
CAN/CSA-Z305.8-2003 Medical Supply Units (First Edition; Update No 1: October 2003)
CSA Z8000-2011 Canadian health care facilities (First Edition; Update No. 1: February 2013)
CSA Z314.7-2003 Steam Sterilizers for Healthcare Facilities (Fourth Edition; Update #1: December 2005)
CSA C22.2 No.60601-2-40-01-2001 Medical Electrical Equipment - Part 2-40: Particular Requirements for the Safety of Electromyographs and Evoked Response Equipment First Edition
CSA Z318.6-95-1995 Commissioning of Medical Gas Systems in Health Care Facilities General Instruction No 1 R(1999)
CAN/CSA-Z8001-2013 Commissioning of health care facilities (First Edition; Incorporating Errata: July 2015)
CSA Z314.0-2013 Medical device reprocessing - General requirements (First Edition; Incorporated Errata: March 2014)
CSA Z317.10-2021 Handling of health care waste materials

Lithuanian Standards Office

LST EN 60601-2-40-2000 Medical electrical equipment. Part 2-40: Particular requirements for the safety of electromygraphs and evoked response equipment (IEC 60601-2-40:1998)
LST EN 62127-1-2008 Ultrasonics - Hydrophones - Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz (IEC 62127-1:2007)

NATO - North Atlantic Treaty Organization

STANAG 2060-1984 Identification of Medical Materiel for Field Medical Installations (ED 2 AMD 3 Amendment 3: 05/27/1994)
STANAG 2347-1975 Medical Warning Tag (ED 1 AMD 6 Amendment 6: 05/21/1996)
STANAG 2060-2006 Identification of Medical Materiel for Field Medical Installations (ED 3)
AJMEDP-3-2008 ALLIED JOINT MEDICAL DOCTRINE FOR MEDICAL INTELLIGENCE
STANAG 2060-2014 IDENTIFICATION DES MAT?RIELS M?DICAUX DES UNIT?S M?DICALES OP?RATIONNELLES (ED 5)
STANAG 7112-2011 RECOMMENDED MEDICAL EQUIPMENT FOR AEROMEDICAL EVACUATIONS (ED 1)

European Committee for Electrotechnical Standardization（CENELEC）

EN 60601-2-40:1998 Medical Electrical Equipment Part 2-40: Particular Requirements for the Safety of Electromyographs and Evoked Response Equipment
EN 62127-1:2007 Ultrasonics - Hydrophones - Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz

US-FCR

FCR FED H-08-4 VOL 1 47A-1979 THERAPEUTIC POOL 40'.0" L X 33'.0" W
FCR AF 91-8-1998 MEDICAL FACILITIES
FCR COE EP 385-1-58-1982 MEDICAL SURVEILLANCE HANDBOOK
FCR FED H-08-1 SEC 16665-2005 MISCELLANEOUS MEDICAL SYSTEMS
FCR VA 27 52 41-2005 MISCELLANEOUS MEDICAL SYSTEMS
FCR UFGS-11 72 13-2006 MEDICAL EQUIPMENT, MISCELLANEOUS
FCR FED FCGS 11702-1986 MEDICAL EQUIPMENT, MISCELLANEOUS
FCR FED H-08-9 CHAP 246-1980 MEDICAL ADMINISTRATION SERVICE
FCR FED H-08-5 CHAP 246-1978 MEDICAL ADMINISTRATION SERVICE

Association Francaise de Normalisation

NF X30-507:2018 Packaging for medical waste - Medical waste - Cardboard box with inner bag for infectious medical waste
NF EN 16844+A2:2019 Services en médecine esthétique - Traitements médicaux, non chirurgicaux
NF S99-401:1994 Dispositifs médicaux - Élastomère de silicone de qualité médicale
NF C74-351-1/A1*NF EN 62127-1/A1:2013 Ultrasonics - Hydrophones - Part 1 : measurement and characterization of medical ultrasonic fields up to 40 MHz
NF EN 16844/IN2:2019 Services en médecine esthétique - Traitements médicaux, non chirurgicaux
NF S99-211:2007 Medical devices - Application of risk management to medical devices.
NF S98-116-2*NF ISO 17664-2:2021 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2 : non-critical medical devices
NF S99-211:2013 Medical devices - Application of risk management to medical devices
NF S98-136:2009 Sterilisation of medical devices - Risk management related to the preparation of sterile medical devices within health establishments.
NF C74-054:2008 Medical devices - Application of usability engineering to medical devices.
NF S99-802*NF EN 16224+A1:2014 Healthcare provision by chiropractors
NF S98-116-1*NF EN ISO 17664-1:2021 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1 : critical and semi-critical medical devices
NF EN ISO 14971:2019 Medical devices - Application of risk management to medical devices
NF S99-211/A11*NF EN ISO 14971/A11:2021 Medical devices - Application of risk management to medical devices
NF EN ISO 14971/A11:2021 Medical devices - Application of risk management to medical devices
NF EN IEC 62667:2018 Medical electrical devices - Light ion beam medical devices - Performance characteristics
NF S99-012:2010 Medical devices - Quality management - Medical device nomenclature data structure.
NF C74-393:2000 Medical electrical equipment - Part 2-40 : particular requirements for the safety of electromyographs and evoked response equipments.
XP S98-224*XP ISO/TS 22421:2021 Sterilization of health care products - Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
NF S99-801*NF EN 16686:2015 Osteopathic healthcare provision

US-VA

VA FED H-08-4 VOL 1 47A-1979 THERAPEUTIC POOL 40'.0" L X 33'.0" W

German Institute for Standardization

DIN 58133:2008-07 Medical compression hosiery
DIN EN 62366:2008 Medical devices - Application of usability engineering to medical devices (IEC 62366:2007); German version EN 62366:2008
DIN 58133:2008 Medical compression hosiery
DIN 58846:2017-11 Medical instruments - Raspatories
DIN EN ISO 14971:2007 Medical devices - Application of risk management to medical devices (ISO 14971:2007); German version EN ISO 14971:2007
DIN EN 60601-2-40:1998 Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromygraphs and evoked response equipment (IEC 60601-2-40:1998); German version EN 60601-2-40:1998
DIN 96056:2009 Medical instruments - Bone raspatory
DIN 58852:2021-02 Medical instruments - Probes
DIN EN 16686:2015 Osteopathic healthcare provision
DIN 58794:1982 Medical instruments; ear forceps
DIN 58852:2008 Medical instruments - Probes
DIN EN ISO 17664-1:2021-11 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021); German version EN ISO 17664-1:2021
DIN 13117:2013 Medical instruments.Bone shears
DIN EN 556-1:2002 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; German version EN 556-1:2001
DIN 58857:2019-12 Medical instruments - Directors
DIN 58794:2010 Medical instruments - Ear forceps
DIN 58852:2014 Medical instruments - Probes
DIN 13119:2010 Medical instruments - Bowel scissors
DIN 13117:1980 Medical instruments; bone shears
DIN 58852:2021 Medical instruments - Probes
DIN 13119:1980 Medical instruments; bowel scissors
DIN 58852:1976 Medical instruments; probes

CZ-CSN

CSN 65 6544-1959 medical oil
CSN 66 4710-1974 Medical plaster
CSN 36 4800-1966 Electrical medical insíruments
CSN 86 7027-1959 medical soap fragrance
CSN 40 4318 Za-1987 Revision a-9/1987 Czech National Standard 40 4318, containing radioactive radiation source 8 226Ra for medical needles and tubes
CSN 36 4830-1967 Medical lighting devices

Korean Agency for Technology and Standards (KATS)

KS P 2603-2008(2018) Medical hooks
KS P 2603-1978 Medical hooks
KS P 2009-2009(2019) Medical forceps
KS P 2615-1980 Medical retractor
KS P 2615-2008(2018) Medical retractor
KS P ISO 14971:2021 Medical devices — Application of risk management to medical devices
KS P 2604-2008(2018) Medical curettes
KS P 3502-2019 Medical chisels
KS P 3502-1985 Medical chisels
KS P ISO 14971:2018 Medical devices — Application of risk management to medical devices
KS P ISO TR 14969-2008(2018) Medical devices－Quality management systems－Guidance on the application of KS P ISO 13485:2007
KS P 8405-2018 Medical treadmils
KS P 8405-1987 Medical treadmils
KS P ISO 17664-1:2021 Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical medical devices
KS P ISO 15225-2023 Medical devices — Quality management — Medical device nomenclature data structure

European Committee for Standardization (CEN)

EN 556-1:2001 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices
CENELEC EN 62127-1-2007 Ultrasonics - Hydrophones - Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz
CENELEC EN 62353-2008 Medical electrical equipment — Recurrent test and test after repair of medical electrical equipment
EN ISO 14971:2012 Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
DD ENV 12967-1-1998 Medical Informatics - Healthcare Information System Architecture (HISA) - Part 1: Healthcare Middleware Layer
EN ISO 17664-1:2021 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)
CENELEC EN 62366-2008 Medical devices - Application of usability engineering to medical devices
EN 16686:2015 Osteopathic healthcare provision
EN 556:1994 Sterilization of Medical Devices - Requirements for Medical Devices to Be Labelled `Sterile'
EN 16872:2016 Services of Medical Doctors with additional qualification in Homeopathy (MDQH) - Requirements for health care provision by Medical Doctors with additional qualification in Homeopathy
EN ISO 11197:2009 Medical supply units
EN ISO 11197:2019 Medical supply units (ISO 11197:2019)

BE-NBN

NBN C 74-788-1990 Medical Radiology. Medical radiation terminology. the term
NBN 327-1959 Medical gas identification

AENOR

UNE-ENV 12443:2000 Medical Informatics - Healthcare Information Framework (HIF)
UNE-EN 60601-2-40:1999 MEDICAL ELECTRICAL EQUIPMENT. PART 2-40: PARTICULAR REQUIREMENTS FOR THE SAFETY OF ELECTROMYOGRAPHS AND EVOKED RESPONSE EQUIPMENT.
UNE-EN 62366:2009 Medical devices- Application of usability engineering to medical devices

RU-GOST R

GOST ISO 14971-2011 Medical devices. Application of risk management to medical devices
GOST R ISO 14971-2009 Medical devices. Application of risk management to medical devices
GOST R ISO 14971-2006 Medical devices. Application of risk management to medical devices
GOST R IEC 62366-2013 Medical devices. Application of usability engineering to medical devices
GOST R ISO 15225-2014 Medical devices. Quality management. Medical device nomenclature data structure
GOST R 52976-2008 Health informatics. First database structure of medical statistics of medical entity for electronic exchange of these data. General requirements

Danish Standards Foundation

DS/EN 62127-1:2008 Ultrasonics - Hydrophones - Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz
DS/ENV 12443:2000 Medical Informatics - Healthcare Information Framework (HIF)
DS/EN 62127-1/A1:2013 Ultrasonics - Hydrophones - Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz
DS/ISO/TS 22421:2021 Sterilization of health care products – Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
DS/EN ISO 14971:2013 Medical devices - Application of risk management to medical devices
DS/EN ISO 15225:2010 Medical devices - Quality management - Medical device nomenclature data structure
DS/EN 62366:2008 Medical devices - Application of usability engineering to medical devices
DS/EN ISO 17664-1:2021 Processing of health care products – Information to be provided by the medical device manufacturer for the processing of medical devices – Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)
DS/EN ISO 11197:2009 Medical supply units
DS/CEN/CR 14060:2001 Medical device traceability

ES-UNE

UNE-EN 62127-1:2007/A1:2013 Ultrasonics - Hydrophones - Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz (Endorsed by AENOR in May of 2013.)
UNE-EN 62127-1:2007 Ultrasonics - Hydrophones -- Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz (Endorsed by AENOR in October of 2009.)
UNE-EN ISO 14971:2020/A11:2022 Medical devices - Application of risk management to medical devices (ISO 14971:2019)
UNE-EN ISO 14971:2020 Medical devices - Application of risk management to medical devices (ISO 14971:2019)
UNE-EN ISO/ASTM/TR 52916:2022 Additive manufacturing for medical - Data - Optimized medical image data (ISO/ASTM TR 52916:2022) (Endorsed by Asociación Española de Normalización in March of 2022.)
UNE-EN ISO 17664-1:2022 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)
ISO 7101:2023 Healthcare organization management — Management systems for quality in healthcare organizations — Requirements
UNE-EN ISO 11197:2020 Medical supply units (ISO 11197:2019)

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 TR 60930:2008 Guidelines for administrative, medical, and nursing staff concerned with the safe use of medical electrical equipment and medical electrical systems
IEC 62127-1:2013 Ultrasonics - Hydrophones - Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz

ZA-SANS

SANS 10248-1:2008 Management of healthcare waste - Part 1: Management of healthcare risk waste from a healthcare facility
SANS 18308:2007 Health informatics - Requirements for an electronic health record architecture
SANS 14971:2008 Medical devices - Application of risk management to medical devices
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

U.S. Military Regulations and Norms

ARMY MIL-DTL-3476/13 C VALID NOTICE 3-2013 Brassard, Medical Service, Veterinary Corps
ARMY UFGS 22 00 70-2011 PLUMBING, HEALTHCARE FACILITIES
ARMY UFGS 22 00 70-2010 PLUMBING, HEALTHCARE FACILITIES

CEN - European Committee for Standardization

EN ISO 14971:2009 Medical devices - Application of risk management to medical devices
EN ISO 14971:2007 Medical devices - Application of risk management to medical devices
EN ISO 14971:2000 Medical Devices - Application of Risk Management to Medical Devices (Incorporates Amendment A1: 2003)
EN ISO 14971:2019 Medical devices - Application of risk management to medical devices
EN ISO 11197:2004 Medical supply units
EN 13824:2004 Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements

International Organization for Standardization (ISO)

ISO 14971:2019 Medical devices — Application of risk management to medical devices
ISO 15223-1:2021/CD Amd 1:2024 Medical devices
ISO 11197:2019 Medical supply units
ISO/CD 20417:2024 Medical devices
ISO 14971:2007 Medical devices - Application of risk management to medical devices
ISO 14971:2000 Medical devices - Application of risk management to medical devices
ISO/IEEE 11073-20702:2018 Health informatics — Point-of-care medical device communication — Part 20702: Medical devices communication profile for web services
ISO 17664-1:2021 Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical medical devices
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/FDIS 80601-2-79:2024 Medical electrical equipment
ISO 17664-2:2021 Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices
ISO 15225:2010 Medical devices - Quality management - Medical device nomenclature data structure
ISO 80601-2-55:2018/Amd 1:2023 Medical electrical equipment
ISO/FDIS 80601-2-80:2024 Medical electrical equipment
ISO/DIS 11197:2024 Medical supply units
IEC 80601-2-77:2019/AMD1:2023 Medical electrical equipment
ISO 15225:2016 Medical devices - Quality management - Medical device nomenclature data structure
IEC 80601-2-26:2019/AMD1:2024 Medical electrical equipment
ISO 80601-2-13:2022/AWI Amd 1:2024 Medical electrical equipment
IEC 80601-2-58:2024 Medical electrical equipment
ISO/DIS 5092:2024 Additive manufacturing for medical
ISO/CD 80601-2-90.2:2024 Medical electrical equipment
ISO/TS 17371:2023 Healthcare organization management
ISO/CD 80601-2-74.2:2024 Medical electrical equipment

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

ASHRAE JOURN 40-10 ARR-1998 ASHRAE Research Report 1998-99
ASHRAE JOURN 40-1 ARI-1998 ASHRAE Journal

Japanese Industrial Standards Committee (JISC)

JIS T 14971:2003 Medical devices -- Application of risk management to medical devices
JIS T 2603:1953 Medical hooks
JIS T 14971:2012 Medical devices -- Application of risk management to medical devices

GSO

GSO OIML R26:2007 Medical syringes
GSO ISO 17664-2:2023 Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 2: Non-critical medical devices
GSO ISO 14971:2015 Medical devices -- Application of risk management to medical devices
BH GSO ISO 17664-2:2023 Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 2: Non-critical medical devices
BH GSO ISO 14971:2017 Medical devices -- Application of risk management to medical devices
OS GSO ISO 14971:2015 Medical devices -- Application of risk management to medical devices
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
BH GSO ISO 15225:2017 Medical devices -- Quality management -- Medical device nomenclature data structure
GSO ISO 15225:2016 Medical devices -- Quality management -- Medical device nomenclature data structure
GSO ISO 11197:2021 Medical supply units
BH GSO ISO 11197:2022 Medical supply units

US-AAMI

ANSI/AAMI/ISO 14971:2007 Medical devices - Application of risk management to medical devices

KR-KS

KS P ISO 14971-2018 Medical devices — Application of risk management to medical devices
KS P ISO 14971-2021 Medical devices — Application of risk management to medical devices
KS P ISO 17664-2-2022 Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 2: Non-critical medical devices
KS P ISO 17664-1-2021 Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical medical devices
KS C IEC 60976-2020 Medical electrical equipment — Medical electron accelerators — Functional performance characteristics

International Maritime Organization (IMO)

IMO TA114E-2001 Medical First Aid

American National Standards Institute （ANSI)

ANSI/AAMI/ISO 17664-2:2022 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices
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 17664-1:2022 Processing of health care products -Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices
ANSI P1073.1.3.7/D4.0-1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized – Blood Pressure
ANSI P1073.1.3.8/D4.0-1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized – Temperature

NEMA - National Electrical Manufacturers Association

NEMA CODE OF ETHICS- Code of Ethics - On Interactions with Health Care Providers (Published in 2005)

TH-TISI

TIS 14971-2013 Medical devices.application of risk management to medical devices

US-CFR-file

CFR 42-405.212-2013 Public Health. Part405:Federal health insurance for the aged and disabled. Section405.212:Medicare Coverage IDE study criteria.
CFR 42-405.2466-2014 Public Health. Part405:Federal health insurance for the aged and disabled. Section405.2466:Annual reconciliation.
CFR 42-405.2412-2014 Public Health. Part405:Federal health insurance for the aged and disabled. Section405.2412:Physicians' services.

Standard Association of Australia （SAA）

ISO 5741:2023 Healthcare organization management — Pandemic response — Temporary medical facility
AS/NZS 2500:2020 Safe use of medical electrical equipment in health care
AS ISO 14971:2020 Medical devices — Application of risk management to medical devices
AS/NZS 4434.1:1996 Medical electrical equipment - Medical electron accelerators - Functional performance characteristics

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

IEEE 11073-10207-2017 Health informatics - Point-of-care medical device communication - Part 10207: Domain Information and Service Model for Service-Oriented Point-of-Care Medical Device Communication
IEEE P11073-10101/D8-2019 Standard for Health Informatics—Point-of-Care Medical Device Communication—Nomenclature

North Atlantic Treaty Organization Standards Agency

STANAG 2060-2008 IDENTIFICATION OF MEDICAL MATERIEL FOR FIELD MEDICAL INSTALLATIONS
STANAG 2347-2008 MEDICAL WARNING TAG
STANAG 3204-2007 AEROMEDICAL EVACUATION

AT-ON

ONORM K 2202-1999 Medical informatics - Patient refferal
OENORM EN ISO 17664-1:2021 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO/FDIS 17664-1:2021)
ONORM S 2104-1999 Waste from medical institutions

HU-MSZT

MNOSZ 10340-1952 medical nail brush
MNOSZ 14708-1955 Medical and health equipment

IN-BIS

IS 10550-1983 Medical lamp specifications

GOST

GOST ISO 14971-2021 Medical devices. Application of risk management to medical devices
GOST R IEC 62366-1-2023 Medical devices. Part 1. Application of usabilityengineering to medical devices

Indonesia Standards

SNI IEC 60601-2-40:2009 Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment
SNI 16-4940.1-1998 Electrically powered medical suction equipment
SNI 16-4940.2-1998 Medical suction equipment powered from vacuum or pressure sources

National Electrical Manufacturers Association（NEMA)

NEMA CODE OF ETHICS Code of Ethics - On Interactions with Health Care Providers Published in 2005

PL-PKN

PN Z78000-1970 Medical equipmen< opular hospital beds
PN Z78006-1972 Medksal tretchers

CENELEC - European Committee for Electrotechnical Standardization

EN 62366:2008 Medical devices - Application of usability engineering to medical devices

DIN

DIN EN ISO 17664-2:2024 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021); German version EN ISO 17664-2:2023

CH-SNV

SN EN ISO 17664-1:2021 Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)