Personalized Medicine

Personalized Medicine, Total:200 items.

The international standard classification for "Personalized Medicine" includes: Medical equipment , Medical equipment in general , Finances. Banking. Monetary systems. Insurance .

The Chinese standard classification for "Personalized Medicine" includes: Medical apparatus and devices in general , Finance and Insurance .

Group Standards of the People's Republic of China

T/CAMDI 062-2021 Special requirements for 3D modeling software for additive manufacturing of personalized medical devices
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
T/CACM 1407-2022 Guidelines for diagnosis and treatment of colorectal cancer during chemotherapy with traditional Chinese medicine intervention
T/GDWJ 020-2023 Service specification of medical nursing assistant in medical institution
T/CAMDI 026-2024 Special Requirements of Quality Management System for Additive Manufacturing Personalized Medical Devices
T/GXAS 871-2024 Specification for management of medical nursing assistants of medical institutions
T/GDNS 007-2023 Medical and Health Personal Information Protection Specifications
T/CACM 1576-2024 Guideline on the diagnosis and treatment of live cirrhosis by traditional Chinese medicine
T/CAMDI 029-2024 Additive Manufacturing-General requirements for Medical-Engineering Interaction of Personalized Medical Devices
T/CAMDI 025-2024 Additive Manufacturing-Mechanical Equivalent Model of Personalized Medical Devices

Professional Standard - Medicine

YY/T 0802.2-2024 Disposal of medical devices - Information to be provided by the medical device manufacturer - Part 2: Low-risk medical devices
YY/T 1474-2016 Medical devices－Application of risk management to medical devices
YY/T 0316-2003 Medical devices -- Application of risk management to medical devices
YY/T 0802.1-2024 Disposal of medical devices Information to be provided by the medical device manufacturer Part 1: Medium and high risk medical devices

Jilin Provincial Standard of the People's Republic of China

DB22/T 3460-2023 TCM diagnosis and treatment standard for myelosuppression after radiotherapy and chemotherapy

Anhui Provincial Standard of the People's Republic of China

DB34/T 5124-2025 Medical waste management regulations for medical and health institutions

Tianjin Provincial Standard of the People's Republic of China

DB12/ 597-2015 Regulations on Medical Waste Treatment in Medical and Health Institutions
DB12/T 597-2025 Specification for the Management of Medical Waste in Healthcare Institutions

Zhejiang Provincial Standard of the People's Republic of China

DB3311/T 237-2023 Technical specifications for artificial breeding of horsemouth

Jiangsu Provincial Standard of the People's Republic of China

DB32/T 3545.4-2021 Technical Management of Blood Purification Therapy Part 4: Medical Quality Management Standards for Blood Purification Medical Institutions

Taiwan Provincial Standard of the People's Republic of China

CNS 6286-1980 Medical Hooks

Liaoning Provincial Standard of the People's Republic of China

DB21/T 4178-2025 Design Specifications for Temporary Storage Rooms for Medical Waste in Healthcare Institutions

Shandong Provincial Standard of the People's Republic of China

DB37/T 4379-2021 Standard for medical security service of designated medical institution

Gosstandart of Russia

GOST R 59771-2021 Personalized medical devices. Key terms and definitions
GOST R IEC 62366-2013 Medical devices. Application of usability engineering to medical devices
GOST R IEC 62366-1-2023 Medical devices. Part 1. Application of usabilityengineering to medical devices
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 ISO 10993-13-2011 Medical devices. Biological evaluation of medical devices. Part 13. Identification and quantification of degradation products from polymeric medical devices
GOST R ISO 10993-18-2009 Medical devices. Biological evaluation of medical devices. Part 18. Chemical characterization of materials

British Standards Institution (BSI)

PD ISO/TS 6201:2025 Informatique de santé — Cadre de santé numérique personnalisé
BS EN 62366-1:2015+A1:2020 Medical devices. Application of usability engineering to medical devices
BS EN 62366-1:2015 Medical devices. Application of usability engineering to medical devices
BS PD CEN ISO/ASTM/TR 52916:2022 Additive manufacturing for medical. Data. Optimized medical imagedata
BS EN 62366:2008 Medical devices - Application of usability engineering to medical devices
DD ENV 12610-1998 Medical informatics. Medical product identification
DD ENV 12052-1998 Medical informatics. Medical imaging communication (MEDICOM)
BS 1882:1966 Flexible tubing for medical use
BS PD IEC/TR 62366-2:2016 Medical devices. Guidance on the application of usability engineering to medical devices
BS EN 62366:2008+A1:2015 Medical devices. Application of usability engineering to medical devices
BS DD ENV 12443:2001 Medical informatics - Healthcare information framework (HIF)
DD ENV 12017-1998 Medical informatics. Medical informatics vocabulary (MIVoc)
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
BS EN 60976:2008 Medical electrical equipment - Medical electron accelerators - Functional performance characteristics
BS EN 60976:2007 Medical electrical equipment - Medical electron accelerators - Functional performance characteristics
BS EN ISO 14971:2007 Medical devices - Application of risk management to medical devices
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 14971:2009 Medical devices - Application of risk management to medical devices
BS EN ISO 14971:2012 Medical devices. Application of risk management to medical devices
BS DD ENV 13735:2001 Health informatics - Interoperability of patient connected medical devices
BS EN 16224:2012 Healthcare provision by chiropractors
BS DD ENV 12967-1:1998 Medical informatics. Healthcare Information System Architecture (HISA)-Healthcare middleware layer
BS EN ISO 10993-18:2020+A1:2023 Biological evaluation of medical devices - Chemical characterization of medical device materials within a risk management process
DD ENV 12435-2000 Medical informatics. Expression of results of measurements in health sciences

International Organization for Standardization (ISO)

ISO/ASTM TR 52916:2022 Additive manufacturing for medical — Data — Optimized medical image data
ISO 14971:2019 Medical devices — Application of risk management to medical devices
ISO 15223-1:2021/CD Amd 1:2024 Medical devices
ISO 14971:2007 Medical devices - Application of risk management to medical devices
ISO 10993-18:2020/Amd.1:2022 Biological evaluation of medical devices - Chemical characterization of medical device materials within a risk management process
ISO/CD 20417:2024 Medical devices

European Telecommunications Standards Institute (ETSI)

ETSI ES 202 642-2010 Human Factors (HF); Personalization of eHealth systems by using eHealth user profiles (eHealth) (V1.1.1)

Association Francaise de Normalisation

NF X30-507:2018 Packaging for medical waste - Medical waste - Cardboard box with inner bag for infectious medical waste
NF S99-401:1994 Medical Devices - Medical Grade Silicone Elastomer
NF C74-054:2008 Medical devices - Application of usability engineering to medical devices.
NF EN IEC 62667:2018 Medical electrical devices - Light ion beam medical devices - Performance characteristics
NF C74-208/A1:2001 Medical electrical equipment - Medical electron accelerators - Functional performance characteristics.
NF EN 16844+A2:2019 Aesthetic Medicine Services - Medical, Non-Surgical Treatments
NF EN 16844/IN2:2019 Aesthetic Medicine Services - Medical, Non-Surgical Treatments
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 S99-211:2007 Medical devices - Application of risk management to medical devices.
NF S99-211:2013 Medical devices - Application of risk management to medical devices

U.S. Military Regulations and Norms

ARMY UFGS-12 35 70-2010 MEDICAL AND DENTAL CASEWORK
ARMY MIL-DTL-3476/13 C VALID NOTICE 3-2013 Brassard, Medical Service, Veterinary Corps

International Electrotechnical Commission (IEC)

IEC 62366:2007/AMD1:2014 Medical devices - Application of usability engineering to medical devices
IEC 62366:2014 Medical devices - Application of usability engineering to medical devices
IEC 62366:2007 Medical devices - Application of usability engineering to medical devices
IEC 62366:2007+AMD1:2014 CSV Medical devices - Application of usability engineering to medical devices
IEC 62366-1:2015 Medical devices - Part 1: Application of usability engineering to medical devices
IEC TR 62366-2:2016 Medical devices - Part 2: Guidance on the application of usability engineering to medical devices
IEC/TR 62366-2:2016 Medical devices — Part 2: Guidance on the application of usability engineering to medical devices
IEC TR 62366-2-2016 Medical devices — Part 2: Guidance on the application of usability engineering to medical devices

Standard Association of Australia （SAA）

AS 2811:1985 Personal emergency medical information devices
AS 1094:1993 Medical equipment - Single-use syringes (sterile) for general medical use
AS 2696:1989 Medical equipment - Single-use urethral catheters (sterile) for general medical use
AS 2696:1984 Medical equipment - Single-use urethral catheters (sterile) for general medical use

Ente Nazionale Italiano di Unificazione

UNI EN ISO/IEEE 11073-10472:2025 Health informatics - Device interoperability - Part 10472: Personal Health Device Communication - Device Specialization - Medication Monitor
UNI ENV 12967-1:1999 Medical Informatics - Healthcare Information System Architecture (HISA) - Healthcare Middleware Layer
UNI EN 16844:2017 Aesthetic medicine services - Non-surgical medical treatments
UNI EN ISO 14971:2008 Medical devices - Application of risk management to medical devices
UNI CEI EN ISO 14971:2002 Medical devices - Application of risk management to medical devices
UNI CEI EN ISO 14971:2004 Medical devices - Application of risk management to medical devices
UNI CEI EN ISO 14971:2012 Medical devices - Application of risk management to medical devices
UNI 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

Spanish Association for Standardization (UNE)

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 62366:2009 Medical devices- Application of usability engineering to medical devices
UNE-ENV 12443:2000 Medical Informatics - Healthcare Information Framework (HIF)
UNE-EN 60336:2006 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots
UNE-CR 14060:2001 Medical device traceability.

American National Standards Institute （ANSI)

ANSI/AAMI/IEC 62366:2007 Medical devices - Application of usability engineering to medical devices
ANSI/CGA M-1-2025 Standard for Medical Gas Supply Systems at Health Care Facilities
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
ANSI/AAMI/IEC 62366/A1:2014 Medical devices - Application of usability engineering to medical devices - Amendment 1
ANSI P1073.1.3.11/D3.0-1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized – Capnometer

Association for the Advancement of Medical Instrumentation

AAMI TIR18:2010 Guidance on electromagnetic compatibility of medical devices in healthcare facilities
AAMI/IEC 62366:2007 Medical devices - Application of usability engineering to medical devices
AAMI/IEC 62366:2007(R2013) Medical devices - Application of usability engineering to medical devices
ANSI/AAMI/ISO 14971:2007 Medical devices - Application of risk management to 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

GCC Standardization Organization

GSO ISO 29585:2024 Health informatics — Framework for healthcare and related data reporting
GSO IEC 62366:2014 Medical devices - Application of usability engineering to medical devices
BH GSO ISO 14971:2024 Medical devices — Application of risk management to medical devices
OS GSO ISO 14971:2024 Medical devices — Application of risk management to medical devices
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 OIML R26:2007 Medical syringes
GSO IEC 62366-1:2015 Medical devices - Part 1: Application of usability engineering to medical devices
GSO ISO 14971:2015 Medical devices -- Application of risk management to medical devices

German Institute for Standardization

DIN EN 62366:2008 Medical devices - Application of usability engineering to medical devices (IEC 62366:2007); German version EN 62366:2008
DIN 58133:2008-07 Medical compression hosiery

Czech Standards Institute (UNMZ)

CSN 84 6620-1955 Metal pair medical device box (two wings)
CSN 65 6544-1959 medical oil

Institute of Electrical and Electronics Engineers (IEEE)

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 P1073.1.3.11/D3.0:1999 Draft Standard for Medical Device Communications - Medical Device Data Language (MDDL) Virtual Medical Device, Specialized - Capnometer
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
IEEE Std P1073.1.3.10/D3.0-1999 IEEE Draft Standard for Medical Device Communications -- Medical Device Data Language (MDDL) Virtual Medical Device, Specialized -- Cardiac Output

US Federal Contractor Registration (USFCR)

FCR UFGS-11 82 21-2008 MEDICAL WASTE INCINERATORS
FCR AF 91-8-1998 MEDICAL FACILITIES

Military Standards (MIL-STD)

MIL MIL-C-42068-1989 CHEST, MEDICAL INSTRUMENT AND SUPPLY SET

Canadian Standards Association (CSA)

CSA Z314.23-16:2016 Chemical sterilization of reusable medical devices in healthcare settings
CSA Z317.10-2009(R2014) Handling of waste materials in health care facilities and veterinary health care facilities
CSA Z16686-2020(R2021) Chiropractic Medical Services
CSA Z314.23-2012 Sterilization by chemical agent of reusable medical devices in healthcare establishments (first edition)
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

The Directorate General of Specifications and Metrology (DGSM)

OS GSO IEC 62366:2014 Medical devices - Application of usability engineering to medical devices

International Telecommunication Union (ITU)

ITU-T H.813-2017 Interoperability design guidelines for personal connected health systems: Healthcare Information System interface (Study Group 16)

Danish Standards Foundation

DANSK DS/EN 62366:2008 Medical devices - Application of usability engineering to medical devices
DANSK DS/EN 62366/A1:2008 Medical devices - Application of usability engineering to medical devices
DS/EN 62366:2008 Medical devices - Application of usability engineering to medical devices
DANSK DS/EN 16844+A2:2019 Aesthetic medicine services – Non-surgical medical treatments
DANSK DS/EN 16844+A1:2018 Aesthetic medicine services – Non-surgical medical treatments
DS/ENV 12443:2000 Medical Informatics - Healthcare Information Framework (HIF)

European Committee for Standardization (CEN)

CENELEC EN 62366-2008 Medical devices - Application of usability engineering to medical devices
EN ISO 14971:2009 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 14971:2012 Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
CENELEC EN 62353-2008 Medical electrical equipment — Recurrent test and test after repair of medical electrical equipment
EN ISO 14971:2007 Medical devices - Application of risk management to medical devices
EN ISO 14971:2019 Medical devices - Application of risk management to medical devices

South African Bureau of Standard

SANS 10248-2:2009 Management of healthcare waste - Part 2: Management of healthcare risk waste for healthcare facilities and healthcare providers in rural and remote settings
SANS 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

European Committee for Electrotechnical Standardization（CENELEC）

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

Comitato Elettrotecnico Italiano

CEI EN 62366/A1:2008 Medical devices - Application of usability engineering to medical devices
CEI EN 62366:2008 Medical devices - Application of usability engineering to medical devices

Korean Agency for Technology and Standards (KATS)

KS P 2603-2008(2018) Medical hooks
KS C IEC 60976-2020 Medical electrical equipment — Medical electron accelerators — Functional performance characteristics
KS P 2603-1978 Medical hooks
KS C IEC 60976:2020 Medical electrical equipment — Medical electron accelerators — Functional performance characteristics
KS P ISO 14971-2018 Medical devices — Application of risk management to medical devices
KS P 2615-2008(2018) Medical retractor
KS P 2615-1980 Medical retractor
KS P 3502-2024 Medical chisels
KS P ISO 14971:2021 Medical devices — Application of risk management to medical devices
KS P 2009-2009(2019) Medical forceps
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

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

AS/NZS 4434.1:1996 Medical electrical equipment - Medical electron accelerators - Functional performance characteristics

Swedish Institute for Standards

SIS SS-IEC 976:1991 Medical electrical equipment — Medical electron accelerators — Functionalperformance charactetistics
SS 8760002:2018 Health care textiles - Fabrics for use in health care - Characteristics, testing and inspection
SS-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)
SIS-ISO/TS 22421:2021 Sterilization of health care products - Common requirements for sterilizers forterminal sterilization of medical devices in health care facilities (ISO/TS 22421:2021)
SS 8752430:2017 Medical gas pipeline systems - Connectors for medical gases

Society of Automotive Engineers (SAE)

SAE J3020_201405 Medical Device Shot Peening

Belgian Standards Institute

NBN C 74-788-1990 Medical Radiology. Medical radiation terminology. the term

National Standards Authority of Ireland

I.S. 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)
I.S. EN 62366-1:2015/A1:2020 Medical devices - Part 1: Application of usability engineering to medical devices

Standards Norway

NS-ENV 12612:1997 Medical informatics — Messages for the exchange of healthcare administrative information
NS 683:1980 Medical test tubes

Indonesia Standards

SNI ISO 17664-2:2021 Pemrosesan produk pelayanan kesehatan — Informasi yang disertakan oleh produsen alat kesehatan untuk pemrosesan alat kesehatan — Bagian 2: Alat kesehatan non-kritikal (ISO 17664-2:2021, IDT)

North Atlantic Treaty Organization Standards Agency

STANAG 2060-2014 IDENTIFICATION OF MEDICAL EQUIPMENT IN OPERATING MEDICAL UNITS (ED 5)
STANAG 2060-2006 Identification of Medical Materiel for Field Medical Installations (ED 3)
AJMEDP-3-2008 ALLIED JOINT MEDICAL DOCTRINE FOR MEDICAL INTELLIGENCE

Association of German Mechanical Engineers

VDI-EE 5702 BLATT 3-2024 Medizinprodukte-Software - Medical SPICE - Empfehlungen fuer die Softwareentwicklung
VDI/VDE 2426 Blatt 2-1995 Standardized catalogue of medical devices

Association for Electrical, Electronic & Information Technologies (VDE)

DIN EN IEC 60601-2-68:2025-12*VDE 0750-2-68:2025-12 Medical electrical equipment
DIN EN IEC 60601-2-83:2026-03*VDE 0750-2-83:2026-03 Medical electrical equipment
DIN EN 60601-1/A13:2025-03*VDE 0750-1/A13:2025-03 Medical electrical equipment
DIN VDE V 0100-710-1:2025-10*VDE V 0100-710-1:2025-10 Medical locations
DIN EN IEC 60601-2-21:2025-07*VDE 0750-2-21 Berichtigung 1:2025-07 Medical electrical equipment

Japanese Industrial Standards Committee (JISC)

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

Kingdom of Bahrain Testing and Metrology Directorate

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

International Maritime Organization (IMO)

IMO TA114E-2001 Medical First Aid

Türk Standardları Enstitüsü

TS EN ISO 17664-1:2021 Processing of healthcare products - Information provided by medical device manufacturers for the processing of medical devices - Part 1: Critical and semi-critical medical devices

Canadian General Standards Board （CGSB)

CAN/HSO 83001:2018 Telehealth

Thai Industrial Standards Institute (TISI)

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