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in vitro extrapolation

in vitro extrapolation, Total:150 items.

The international standard classification for "in vitro extrapolation" includes: Plants and equipment for the food industry , Fire-fighting , Laboratory medicine , Surgical instruments and materials , Piping and couplings .

The Chinese standard classification for "in vitro extrapolation" includes: Other food processing machinery , Medical laboratory equipment , Medical apparatus and devices in general , Hydraulic and pneumatic device , Sanitation in general .


Professional Standard - Agriculture

  • NY/T 3401-2018 Washing device for inside & outside of poultry carcass

Professional Standard - Business

Group Standards of the People's Republic of China

  • T/CCPITCSC 131-2023 Integration of domestic and foreign trade—Evaluation specifications of intelligent adapted for the elderly
  • T/QGCML 239-2021 Outdoor sliding canopy
  • T/CCPITCSC 130-2023 Integration of domestic and foreign trade-Evaluation specification of commodity adapted for the elderly
  • T/FJSX 0001-2023 Double hot-melt plastic steel lining covered with integrated reinforced pipe
  • T/CECS 10104-2020 Insulated decorative panel for external wall of building

Taiwan Provincial Standard of the People's Republic of China

  • CNS 13382-5-2004 Implants for surgery - Metallic materials - Unalloyed titanium
  • CNS 13382-1-2004 Implants for surgery - Metallic materials - Wrought stainless steel
  • CNS 13382-4-2004 Implants for surgery - Metallic materials - Wrought cobalt-nickel-chromium-molybdenum alloy
  • CNS 13382.1-2004 Implants for surgery - Metallic materials - Wrought stainless steel
  • CNS 13382-2-2004 Implants for surgery - Metallic materials - Wrought cobalt-chromium-tungsten-nickel alloy
  • CNS 12510-1989 Non-dispersed Infrared Gas Analyzer
  • CNS 13382.4-2004 Implants for surgery - Metallic materials - Wrought cobalt-nickel-chromium-molybdenum alloy
  • CNS 13382.5-2004 Implants for surgery - Metallic materials - Unalloyed titanium
  • CNS 13382-6-2004 Implants for surgery - Metallic materials - Cobalt-chromium-molybdenum casting alloy
  • CNS 13382.6-2004 Implants for surgery - Metallic materials - Cobalt-chromium-molybdenum casting alloy
  • CNS 13382.2-2004 Implants for surgery - Metallic materials - Wrought cobalt-chromium-tungsten-nickel alloy

Professional Standard - Petroleum

  • SY/T 6306-1997 Fighting fires in and around flammable and combustible liquid atmospheric strorage tanks

国家药品监督管理局

  • YY/T 1579-2018 In vitro diagnostic medical devices—Evaluation of stability of in vitro diagnostic reagents

Professional Standard - Medicine

  • YY/T 1434-2016 Medical devices for human in vitro assisted reproductive technology—In vitro mouse embryo assay

国家市场监督管理总局、中国国家标准化管理委员会

  • GB/T 2351-2021 Fluid power systems and components-Outside diameters of tubes and inside diameters of hoses
  • GB/T 38137-2019 Guidelines for in vitro screening of nucleic acid aptamers

Professional Standard - Hygiene

Jiangsu Provincial Standard of the People's Republic of China

  • DB32/T 3908-2020 In Vitro Measurement of Thyroid Iodine-131 Activity in Occupational Internal Radiation

United States Navy

YU-JUS

Association Francaise de Normalisation

  • NF ISO 104:2016 Roulements - Butées - Dimensions d'encombrement, plan général
  • NF E22-320:2002 Rolling bearings - Thrust bearings - Boundary dimensions, general plan.
  • NF S90-550:1986 Medico-surgical equipment. External breast prostheses.
  • 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 E62-522:1977 Reduction sleeves with tenon drive with external and internal 7/24 taper.
  • NF S92-017:1995 IN VITRO DIAGNOSTIC SYSTEMS. REQUIREMENTS FOR USER MANUALS FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR HOME USE. (EUROPEAN STANDARD EN 592).
  • NF ISO 3936:2009 Reduction bushings with tenon drive to outer and inner cones 7/24 - Dimensions
  • NF S92-016:1995 IN VITRO DIAGNOSTIC SYSTEMS. REQUIRMENTS FOR USER MANUELS FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR PROFESSIONAL USE. (EUROPEAN STANDARD EN 591).
  • NF ISO 5415:2008 Reduction bushings with 7/24 external and internal Morse cones, with incorporated screw
  • NF S92-010:1992 IN VITRO DIAGNOSTIC SYSTEMS. REQUIREMENTS FOR LABELLING OF IN VITRO DIAGNOSTIC REAGENTS FOR PROFESSIONAL USE. (EUROPEAN STANDARD EN 375).
  • NF S92-011:1992 IN VITRO DIAGNOSTIC SYSTEMS. REQUIREMENTS FOR LABELLING OF IN VITRO DIAGNOSTIC REAGENTS FOR SELF-TESTING. (EUROPEAN STANDARD EN 376).

American National Standards Institute (ANSI)

FI-SFS

  • SFS 5325-1987 wheelchair. Maximum recommended overall size outside user

Korean Agency for Technology and Standards (KATS)

  • KS M ISO 24443-2014(2019) Cosmetics — Sun protection test methods — In vitro determination of UVA protection
  • KS P ISO 23640:2019 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 C 6122-2014 External cardiac pacemaker
  • KS P ISO TR 9325:2013 Implants for surgery-Partial and total hip joint prostheses-Recommendations for simulators for evaluation of hip joint prostheses
  • KS P ISO TR 9325:2008 Implants for surgery-Partial and total hip joint prostheses-Recommendations for simulators for evaluation of hip joint prostheses
  • KS C 6122-1991 External cardiac pacemaker
  • KS P 6123-2006(2021) Electric motor driven blood pump for cardiopulmonary bypass
  • KS V 8840-1987(2012) MARINE SHORE CONNECTION BOXES (SMALL TYPE)

JP-JEITA

  • JEITA ED 7300A-2008 Recommended practice on standard for the preparation of outline drawings of semiconductor package

SCC

  • ABMA/ISO 104-2016 Rolling bearings - Thrust bearings - Boundary dimensions, general plan
  • NS-EN 375:1992 In vitro diagnostic systems — Requirements for labelling of in vitro diagnostic reagents for professional use
  • DANSK DS/EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
  • NS-EN 376:1992 In vitro diagnostic systems — Requirements for labelling of in vitro diagnostic reagents for self-testing
  • NS-EN 592:1994 In vitro diagnostic systems — Requirements for user manual for in vitro diagnostic instruments for home use
  • NS-EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
  • NS-EN ISO 23640:2011 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
  • AENOR UNE-EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
  • NS-EN 591:1994 In vitro diagnostic systems — Requirements for user manuals for in vitro diagnostic instruments for professional use
  • NS-EN ISO 23640:2013 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
  • 09/30210157 DC BS EN ISO 23640. In vitro diagnostic medical devices. Stability testing of in vitro diagnostic reagents

VDI - Verein Deutscher Ingenieure

  • VDI 2631-1968 TESTING INSIDE AND OUTSIDE CONE; TEST METHOD AND TEST MEANS
  • VDI 2343 Blatt 2-1998 Recycling of electrical and electronical products - External and internal logistics

British Standards Institution (BSI)

  • BS ISO 104:2002 Rolling bearings - Thrust bearings - Boundary dimensions, general plan
  • BS EN ISO 23640:2015 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 23640:2013 In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents

International Organization for Standardization (ISO)

  • ISO 104:2015 Rolling bearings - Thrust bearings - Boundary dimensions, general plan
  • ISO 104:2002 Rolling bearings - Thrust bearings - Boundary dimensions, general plan
  • ISO 23640:2011 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
  • ISO/FDIS 8637-3:2023 Extracorporeal systems for blood purification
  • ISO/TR 9325:1989 Implants for surgery; partial and total hip joint protheses; recommendations for simulators for evaluation of hip joint protheses
  • ISO 8637-2:2023 Extracorporeal systems for blood purification

American Bearing Manufacturers Association

  • ABMA 104-1994 Rolling bearings - Thrust bearings - Boundary dimensions, general plan

API - American Petroleum Institute

GM North America

  • GM GMP.E/P.120-2002 Thermoplastic Elastomer Polyolefinic, Shore A80, Interior/Exterior, Integrally Colored
  • GM GMP.E/P.016-2002 Thermoplastic Elastomer Polyolefinic, Shore D50, Interior/Exterior, Integrally Colored
  • GM GMP.E/P.029-2001 Thermoplastic Elastomer Polyolefinic, Shore A67, Interior/Exterior
  • GM GMP.E/P.037-2001 Thermoplastic Elastomer Polyolefinic, Shore A87, Interior/Exterior
  • GM GMP.E/P.082-2002 Thermoplastic Elastomer Polyolefinic, Shore A62, Interior/Exterior
  • GM GMP.E/P.132-2003 Thermoplastic Elastomer Polyolefinic, Shore A75, Interior/Exterior
  • GM GMN8154-2003 Thermoplastic Elastomer Polyolefinic, Shore A65, Interior/Exterior
  • GM GMP.E/P.057-2002 Thermoplastic Elastomer Polyolefinic, Shore A73, Interior/Exterior
  • GM GMP.TES.027-2004 Thermoplastic Elastomer - Styrenic Block Copolymer, Shore A70, Interior/Exterior, Integrally Colored

HU-MSZT

SE-SIS

  • SIS SMS 2511-1974 Freezers for household use. Determination of externat dimensions and internal volumes

GSO

  • GSO ISO 3936:2015 Reduction sleeves with tenon drive with external and internal 7/24 taper -- Dimensions
  • GSO ISO 22523:2015 External limb prostheses and external orthoses -- Requirements and test methods
  • GSO ISO 14949:2015 Implants for surgery -- Two-part addition-cure silicone elastomers

RU-GOST R

  • GOST R ISO 23640-2015 In vitro medical devices. Evaluation of stability of in vitro diagnostic reagents

CZ-CSN

US-FCR

Japanese Industrial Standards Committee (JISC)

Military Standards (MIL-STD)

ES-UNE

  • UNE-EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)

Defense Logistics Agency

KR-KS

  • KS P ISO 22523-2016 External limb prostheses and external orthoses — Requirements and test methods
  • KS P ISO 23640-2019 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents

AT-ON

  • ONORM EN 375-1993 In vitro diagnostic Systems - Requirements for labelling of in vitro diagnostic reagents for professional use
  • ONORM EN 376-1993 In vitro diagnostic Systems - Requirements for labelling of in vitro diagnostic reagents for serf-testing
  • ONORM M 6329 Teil.1-1988 Rolling bearings; housings; plummer block (pillow block) housings

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 6855-1:1992 Quality control of nuclear medicine instruments; radiation counting systems for measurements in vivo and in vitro

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 375:1992 In vitro diagnostic systems; requirements for labelling of in vitro diagnostic reagents for professional use
  • EN 376:1992 In vitro diagnostic systems; requirements for labelling of in vitro diagnostic reagents for self-testing
  • EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)

BE-NBN

  • NBN EN 591-1995 In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional use
  • NBN EN 592-1995 In vitro diagnostic systems - Requirements for user manual for in vitro diagnostic instruments for home use
  • NBN-EN 376-1992 In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testing

U.S. Military Regulations and Norms

AIA/NAS - Aerospace Industries Association of America Inc.

ES-AENOR

Danish Standards Foundation

  • DS/EN 375:1993 In vitro diagnostic systems. Requirements for labelling of in vitro diagnostic reagents for professional use
  • DS/EN 376:1993 In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testing
  • DS/EN 591:1995 In vitro diagnostic systems - Requirements for ser manuals for in vitro diagnostic instruments or professional use
  • DS/EN 592:1995 In vitro diagnostic systems - Requirements for ser manuals for in vitro diagnostic instruments or home use

AENOR

  • UNE 48078:1960 ASPECT OF TRANSPARENT LIQUIDS
  • UNE-EN ISO 23640:2013 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)

European Telecommunications Standards Institute (ETSI)

  • ETSI ETR 227-1995 Multimedia Applications and Services; Inband and Outband Signalling Protocols; a Survey

American Society for Testing and Materials (ASTM)

  • ASTM F2477-24 Standard Test Methods for in vitro Pulsatile Durability Testing of Vascular Stents and Endovascular Prostheses

(U.S.) Joint Electron Device Engineering Council Soild State Technology Association