medical diagnosis basis

medical diagnosis basis, Total:200 items.

The international standard classification for "medical diagnosis basis" includes: Laboratory medicine .

The Chinese standard classification for "medical diagnosis basis" includes: Medical laboratory equipment , Medical apparatus and devices in general .

Group Standards of the People's Republic of China

T/CASMI 003-2024 Diagnostic Standards for Renal RI-RADS in Chongqing Social Medical Institutions
T/CASMI 009-2024 Diagnostic Standards for Head-RADS in Chongqing Social Medical Institutions
T/CASMI 005-2024 Diagnostic Standards for Hepatic LI-RADS in Chongqing Social Medical Institutions
T/SZKJKH 015-2023 Anorectal Disease Outpatient Intelligent Medical Treatment Standard
T/IMAAMM 003-2023 Criteria of diagnosis and therapeutic effect of diseases and syndromes in Mongolian Medicine
T/CASMI 010-2024 Diagnostic Standards for NI-RADS in Chongqing Social Medical Institutions
T/BIA 23-2024 Orthopaedic disease diagnosis and treatment dataset - Replantation of amputated finger and limb
T/CIATCM 045-2019 Basic datasets for the Information of knowledge base in Traditional Chinese Medicine section in primary medical and health care institution
T/CASMI 006-2024 Diagnostic Standards for Bone-RADS in Chongqing Social Medical Institutions
T/CASMI 011-2024 Diagnostic Standards for RADS in Chongqing Social Medical Institutions
T/SNEIA 15-2024 Technical Guidelines for Energy Diagnosis of Medical Public Buildings
T/CIET 1018-2025 Technical requirements for auxiliary diagnosis system for smart medical care
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/SAMD 0002-2023 Probes for in-vitro diagnostic medical devices
T/SZZX 014-2023;T/SAMD 0002-2 Pipette Needle for In Vitro Diagnostic Medical Devices
T/CASMI 006-2023 Diagnostic Standards for Colic C-RADS in Chongqing Social Medical Institutions
T/SZZX 014-2023 Probes for in-vitro diagnostic medical devices
T/CIATCM 094-2020 Data interface technical specification in Traditional Chinese Medicine section in primary medical and health care institution
T/CIATCM 053-2019 Basic datasets for teleconsultation in Traditional Chinese Medicine section in primary medical and health care institution
T/CASMI 001-2024 Diagnostic Standards for Breast BI-RADS in Chongqing Social Medical Institutions
T/CIATCM 051-2019 Basic datasets for the platform of preventive treatment of diseases in Traditional Chinese Medicine section in primary medical and health care institution
T/CIATCM 041-2019 Basic datasets for electronic medical records of Traditional Chinese Medicine section in primary medical and health care institution
T/CEMA 015-2025 Guizhou Ethnic Medicine Specialty Clinic Construction Guide
T/CASMI 004-2023 Diagnostic criteria for ovarian O-RADS in social medical institutions in Chongqing

Professional Standard - Medicine

YY/T 1441-2016 General requirements of performance evaluation of in vitro diagnostic medical devices
YY/T 1579-2018 In vitro diagnostic medical devices—Evaluation of stability of in vitro diagnostic reagents
YY/T 1454-2016 General requirements for in vitro diagnostic medical devices for self-testing

Professional Standard - Commodity Inspection

SN/T 1430.1-2004 Rules for the inspection of medical electrical equipment for improt - Ultrasonic medical diagnostic and therapy equipment

Henan Provincial Standard of the People's Republic of China

DB41/T 2621-2024 Prenatal diagnosis (screening) technical medical institution service specifications

Shanghai Provincial Standard of the People's Republic of China

DB31/T 1569.1-2025 Technical requirements for clinical medical data exchange interfaces in medical institutions—Part 1:Emergency data

Czech Standards Institute (UNMZ)

CSN 36 4860-1975 Ultrasonic protes for medical diagnosing

Korean Agency for Technology and Standards (KATS)

KS P ISO 23640-2019(2024) In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
KS P ISO 23640:2019 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
KS P ISO 23640-2019 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
KS P ISO 23640-2024 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
KS P ISO 23640:2013 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
KS P IEC 60601-2-33-2003 Magnetic resonance equipment for medical diagnosis
KS C IEC 60336-2017 Medical electrical equipment — X-ray tube assemblies for medical diagnosis — Characteristics of focal spots
KS C 9708-1997(2017) Phantoms for magnetic resonance equipment for medical diagnosis
KS C 9707-2021 Graphical symbols and sign for magnetic resonance equipment for medical diagnosis
KS P ISO 19001-2017(2022) In virto diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology

Spanish Association for Standardization (UNE)

UNE-EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
UNE-EN 13612/AC:2003 Performance evaluation of in vitro diagnostic medical devices.
UNE-EN ISO 23640:2013 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
UNE-EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices.
UNE-EN 60336:2006 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots
UNE 20-570-1989 Characteristics of X-ray tube focus for medical diagnosis
UNE-EN 61157:2007 Standard means for the reporting of the acoustic output of medical diagnostic ultrasonic equipment
UNE-EN 13532:2002 General requirements for in vitro diagnostic medical devices for self-testing.
UNE-EN 61157:1996 REQUIREMENTS FOR THE DECLARATION OF THE ACOUSTIC OUTPUT OF MEDICAL DIAGNOSTIC ULTRASONIC EQUIPMENT.
UNE-EN 61157:2007/A1:2013 Standard means for the reporting of the acoustic output of medical diagnostic ultrasonic equipment (Endorsed by AENOR in May of 2013.)

Ente Nazionale Italiano di Unificazione

UNI EN ISO 23640:2013 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
UNI EN ISO 23640:2012 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
UNI EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
UNI EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
UNI EN ISO 18113-5:2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self- testing
UNI EN ISO 18113-4:2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self- testing
UNI EN 13532:2002 General requirements for in vitro diagnostic medical devices for self- testing

Bureau of Indian Standards

IS/ISO 23640-2011 In Vitro Diagnostic Medical Devices —— Evaluation of Stability of in vitro Diagnostic Reagents
IS/IEC/TS 80004-7-2011 Nanotechnologies Vocabulary Part 7 Diagnostics and Therapeutics for Healthcare
IS 17719-2023 In-Vitro Diagnostic (IVD) Medical Device - Automatic Slide Staining Instrument
IS/IEC 60336-2005 Medical Electrical Equipment - X-Ray Tube Assemblies for Medical Diagnosis - Characteristics of Focal Spots

British Standards Institution (BSI)

BS EN ISO 23640:2013 In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
BS EN ISO 23640:2011 In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
BS EN ISO 23640:2015 In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
DD ISO/TS 80004-7:2011 Nanotechnologies. Vocabulary. Diagnostics and therapeutics for healthcare
BS DD ISO/TS 80004-7:2011 Nanotechnologies. Vocabulary. Diagnostics and therapeutics for healthcare
BS EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
BS EN 13612:2002(2003) Performance evaluation of in vitro diagnostic medical devices
BS 7555:1992 Guide to miniaturization of medical diagnostic images on film
BS EN 60601-2-33:1996 Medical electrical equipment. Particular requirements for safety-Specification for magnetic resonance equipment for medical diagnosis
09/30210157 DC BS EN ISO 23640. In vitro diagnostic medical devices. Stability testing of in vitro diagnostic reagents
BS PD IEC/TR 62799:2013 Models for evaluation of thermal hazard in medical diagnostic ultrasonic fields
PD IEC/TR 62799:2013 Models for evaluation of thermal hazard in medical diagnostic ultrasonic fields
BS EN ISO 18113-4:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic reagents for self-testing
BS EN 12376:1999 In Vitro Diagnostic Medical Devices - Information Supplied by the Manufacturer with in Vitro Diagnostic Reagents for Staining in Biology
BS EN ISO 18113-2:2009 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic reagents for professional use
BS EN ISO 18113-3:2009 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic instruments for professional use
BS EN ISO 18113-4:2009 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic reagents for self-testing
BS EN ISO 18113-4:2024 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) - In vitro diagnostic reagents for self-testing
BS EN ISO 18113-3:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for professional use
BS EN ISO 18113-5:2024 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) - In vitro diagnostic instruments for self-testing
BS EN 60336:2005 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots
BS EN ISO 18113-5:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for self-testing
BS EN ISO 18113-2:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic reagents for professional use

German Institute for Standardization

DIN EN ISO 23640:2015-12 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011); German version EN ISO 23640:2015 / Note: DIN EN ISO 23640 (2013-09) remains valid alongside this standard until 2018-06-30.
DIN EN 13612:2002-08 Performance evaluation of in vitro diagnostic medical devices; German version EN 13612:2002, German and English texts
DIN EN ISO 23640:2012-03 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
DIN EN ISO 23640:2013-09 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
DIN EN 13532:2002-08 General requirements for in vitro diagnostic medical devices for self-testing; German version EN 13532:2002, German and English texts
DIN EN ISO 23640 E:2013 Draft Document - In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011); German version EN ISO 23640:2013
DIN EN ISO 23640 E:2013-04 Draft Document - In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011); German version EN ISO 23640:2013
DIN ISO/TS 80004-7:2012-07*DIN SPEC 52400-7:2012-07 Nanotechnologies - Vocabulary - Part 7: Diagnostics and therapeutics for healthcare (ISO/TS 80004-7:2011)
DIN EN ISO 18113-5:2010 In vitro diagnostic medical devices — information provided by the manufacturer
DIN EN ISO 18113-4:2021-09 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO/DIS 18113-4:2021); German and English version prEN ISO 18113-4:2021 / Note: Date of issue 2021-08-06...
DIN EN ISO 18113-2:2021-09 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO/DIS 18113-2:2021); German and English version prEN ISO 18113-2:2021 / Note: Date of issue 2021-0...
DIN EN ISO 18113-2:2010 In vitro diagnostic medical devices — information provided by the manufacturer
DIN EN ISO 18113-3:2013-01 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2011 / Note: DIN EN ISO 18113-3 (2010-05) remain...
DIN EN ISO 18113-1:2021-09 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO/DIS 18113-1:2021); German and English version prEN ISO 18113-1:2021 / Note: Date of issue 2021-08-06*I...
DIN EN ISO 18113-3:2010 In vitro diagnostic medical devices — information provided by the manufacturer
DIN EN ISO 18113-1:2013-01 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009); German version EN ISO 18113-1:2011 / Note: DIN EN ISO 18113-1 (2010-05) remains valid a...
DIN EN ISO 18113-1:2010 In vitro diagnostic medical devices Information provided by the manufacturer
DIN EN ISO 18113-4:2013-01 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009); German version EN ISO 18113-4:2011 / Note: DIN EN ISO 18113-4 (2010-05) remains valid...
DIN EN ISO 18113-5:2013-01 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009); German version EN ISO 18113-5:2011 / Note: DIN EN ISO 18113-5 (2010-05) remains va...
DIN EN ISO 18113-4:2010 In vitro diagnostic medical devices — information provided by the manufacturer
DIN EN ISO 18113-2:2013-01 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009); German version EN ISO 18113-2:2011 / Note: DIN EN ISO 18113-2 (2010-05) remains v...
DIN EN ISO 18113-5:2021-09 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/DIS 18113-5:2021); German and English version prEN ISO 18113-5:2021 / Note: Date of issue 2021-08...
DIN EN ISO 18113-3:2021-09 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO/DIS 18113-3:2021); German and English version prEN ISO 18113-3:2021 / Note: Date of issue 202...
DIN EN 60336:2020 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots (IEC 62B/1138/CDV:2019); German and English version prEN 60336:2019
DIN 58962-2:1994 Medical microbiology - Diagnosis of infections of the lower respiratory tract (LRT) - Part 2: Microscopic examination
DIN EN 12376:1999 In vitro diagnostic medical devices – Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
DIN EN 60336:1996 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots
DIN EN ISO 19001 E:2010-08 Information provided by manufacturers of in vitro diagnostic reagents for biocoloring of in vitro diagnostic medical devices (draft)

Danish Standards Foundation

DANSK DS/EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
DANSK DS/EN 13612/AC:2003 Performance evaluation of in vitro diagnostic medical devices
DANSK DS/EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
DS/EN 60336:2005 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots
DANSK DS/EN 13532:2002 General requirements for in vitro diagnostic medical devices for self-testing
DANSK DS/ISO/TS 80004-7:2011 Nanotechnologies - Vocabulary - Part 7: Diagnostics and therapeutics for healthcare
DANSK DS/IEC TR 62799:2015 Models for evaluation of thermal hazard in medical diagnostic ultrasonic fields
DS/ISO/TS 80004-7:2011 Nanotechnologies - Vocabulary - Part 7: Diagnostics and therapeutics for healthcare

Association Francaise de Normalisation

NF EN ISO 23640:2015 In vitro diagnostic medical devices - Assessment of the stability of in vitro diagnostic reagents
NF S92-032*NF EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
NF S92-032:2014 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
NF EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
NF C74-336:1988 Medical electrical equipment. Ultrasound equipment for diagnostic. Classification of specified diagnostic applications.
NF S92-025*NF EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
NF EN 13532:2002 General requirements for in vitro diagnostic medical devices for self-testing
NF S92-040*NF EN ISO 19001:2013 In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
FD T16-101-7:2011 Nanotechnologies - Vocabulary - Part 7: diagnostics and therapies for healthcare
NF EN IEC 60336:2021 Electromedical devices - Equipped ducts for medical diagnosis - Dimensions of the foci and related characteristics
NF S92-024*NF EN 13532:2002 General requirements for in vitro diagnostic medical devices for self-testing
NF S92-040:1999 In vitro diagnostic medical devices. Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology.
NF C74-116:1996 X-ray tube assemblies for medical diagnosis. Characteristics of focal spots.
NF C74-114*NF EN 60613:2010 Electrical and loading characteristics of X -ray tube assemblies for medical diagnosis.
NF C74-116*NF EN IEC 60336:2021 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Focal spot dimensions and related characteristics
NF C74-122/A2:2008 Medical electrical equipment - Part 2-33 : particular requirements for the safety of magnetic resonance equipment for medical diagnosis.
NF EN 60613:2010 Electrical and charging characteristics of sheaths equipped for medical diagnosis
NF C74-116*NF EN 60336:2005 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots

International Organization for Standardization (ISO)

ISO 23640:2011 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
ISO TS 80004-7:2011 Nanotechnologies - Vocabulary - Part 7: Diagnostics and therapeutics for healthcare
ISO/DIS 15193:2024 In vitro diagnostic medical devices — Requirements for reference measurement procedures

European Committee for Standardization (CEN)

EN ISO 23640:2011 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents [Superseded: CEN EN 13640]
EN ISO 23640:2013 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
EN 12376:1999 In Vitro Diagnostic Medical Devices - Information Supplied by the Manufacturer with in Vitro Diagnostic Reagents for Staining in Biology

US Federal Contractor Registration (USFCR)

FCR FED H-08-9 CHAP 202-1980 DRUG DEPENDENCE TREATMENT CLINIC
FCR FED H-08-5 CHAP 202 TRANSMITTAL NO.163-1985 DRUG DEPENDENCE TREATMENT CLINIC, TRANSMITTAL NO. 163

Swedish Institute for Standards

SS-EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
SS-EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
SS-EN 13532:2003 General requirements for in vitro diagnostic medical devices for self-testing

Gosstandart of Russia

GOST R EN 13612-2010 Performance evaluation of in vitro diagnostic medical devices
GOST R 51352-2013 In vitro diagnostic medical devices. Test methods
GOST R 58437-2019 Examination of quality of medical diagnostic veterinary services. General requirements
GOST R 59901-2021 Medical-social expertise. Expert and rehabilitation diagnostics using special diagnostic equipment in federal institutions of medical and social expertise
GOST R 56331-2014 Medical electrical equipment. Medical diagnostic ultrasonic equipment. Technical requirements for governmental purchases
GOST R EN 13532-2010 General requirements for in vitro diagnostic medical devices for self-testing
GOST R ISO 19001-2013 In vitro diagnostic medical devices. Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
GOST R 50267.33-1999 Medical electrical equipment. Part 2. Particular requirements for the safety of magnetic resonance equipment for medical diagnosis
GOST R IEC 60336-1999 X-ray tube assemblies for medical diagnosis. Characteristics of focal spots
GOST R IEC 60601-2-33-2009 Medical electrical equipment. Part 2-33. Particular requirements for the safety of magnetic resonance equipment for medical diagnosis

National Administration of Traditional Chinese Medicine

ZY/T 001.4-1994 Diagnostic and therapeutic standards for pediatric diseases in traditional Chinese medicine
ZY/T 001.7-1994 Diagnostic and therapeutic standards for anorectal diseases of traditional Chinese medicine
ZY/T 001.8-1994 Standards for diagnosis and efficacy of traditional Chinese medicine dermatology syndromes
ZY/T 001.9-1994 Diagnostic and therapeutic standards for orthopedics and traumatology syndromes in traditional Chinese medicine
ZY/T 001.6-1994 Standards for diagnosis and efficacy of TCM otolaryngology syndromes

Standards Norway

NS-EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices
NS-EN ISO 23640:2011 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
NS-EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
NS-EN ISO 23640:2013 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
NS-EN 13532:2002 General requirements for in vitro diagnostic medical devices for self-testing

Japanese Industrial Standards Committee (JISC)

JIS Z 4831:2000 Protective devices against diagnostic medical X-radiation
JIS Z 4120:2008 Medical electrical equipment -- X-ray tube assemblies for medical diagnosis -- Characteristics of focal spots
JIS Z 4924:2016 Phantoms for magnetic resonance equipment for medical diagnosis
JIS Z 4924:1995 Phantoms for magnetic resonance equipment for medical diagnosis
JIS Z 4951:1999 Particular requirements for the safety of magnetic resonance equipment for medical diagnosis

Belgian Standards Institute

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

Finnish Standards Institute

SFS-EN ISO 23640:2015 In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
SFS-EN 13612+AC:2002 Performance evaluation of in vitro diagnostic medical devices

GCC Standardization Organization

GSO EN 13532:2021 General requirements for in vitro diagnostic medical devices for self-testing
GSO ISO/TS 80004-7:2013 Nanotechnologies -- Vocabulary -- Part 7: Diagnostics and therapeutics for healthcare
GSO IEC/TR 62799:2017 Models for evaluation of thermal hazard in medical diagnostic ultrasonic fields
GSO IEC 60336:2015 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots
GSO ISO 19001:2015 In vitro diagnostic medical devices -- Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology

Kingdom of Bahrain Testing and Metrology Directorate

BH GSO EN 13532:2022 General requirements for in vitro diagnostic medical devices for self-testing
BH GSO ISO/TS 80004-7:2016 Nanotechnologies -- Vocabulary -- Part 7: Diagnostics and therapeutics for healthcare

International Electrotechnical Commission (IEC)

IEC 60336:2005 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots
IEC 60336:2020 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Focal spot dimensions and related characteristics

The Directorate General of Specifications and Metrology (DGSM)

OS GSO IEC/TR 62799:2017 Models for evaluation of thermal hazard in medical diagnostic ultrasonic fields
OS GSO ISO/TS 80004-7:2013 Nanotechnologies -- Vocabulary -- Part 7: Diagnostics and therapeutics for healthcare

Comitato Elettrotecnico Italiano

CEI 62-131:2004 Guide to the interpretation of safety indices in medical ultrasound diagnostics

European Committee for Electrotechnical Standardization（CENELEC）

HD 509 S1-1988 Characteristics of Focal Spots in Diagnostic X- Ray Tube Assemblies for Medical Use
EN IEC 60336:2021 Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Focal spot dimensions and related characteristics
EN 60336:1995 X-Ray Tube Assemblies for Medical Diagnosis Characteristics of Focal Spots

Indonesia Standards

SNI ISO 23640:2018 In Vitro Diagnostic Medical Devices – Evaluation of the Stability of In Vitro Diagnostic Reagents (ISO 23640:2011, IDT)

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

AS/NZS 4274:1995 X-ray tube assemblies for medical diagnosis - Characteristics of focal spots
AS/NZS 4184.2.4:1995 Evaluation and routine testing in medical imaging departments - Constancy tests - Hard copy cameras
AS/NZS 4543.1:1999 Protective Medical Devices Against Diagnostic Medical X-Radiation Part 1: Determination of Attenuation Properties of Materials

Lithuanian Standards Office

LST EN 60336-2005 Medical electrical equipment. X-ray tube assemblies for medical diagnosis. Characteristics of focal spots (IEC 60336:2005)

National Electrical Manufacturers Association（NEMA)

NEMA XR 19-1993(R1999) Electrical, Thermal and Loading Characteristics of X-Ray Tubes Used for Medical Diagnosis