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In vitro/be

In vitro/be, Total:420 items.

In the international standard classification, In vitro/be involves: Construction materials, Products of the chemical industry, Electronic components in general, Fuels, Laboratory medicine, Medical equipment, Medical sciences and health care facilities in general, Analytical chemistry, Aircraft and space vehicles in general, Plant and equipment for the food industry, Shipbuilding and marine structures in general, Biology. Botany. Zoology, Vocabularies, Aids for disabled or handicapped persons, Hospital equipment, Fibre optic communications, Linear and angular measurements, Protection of and in buildings, Electricity. Magnetism. Electrical and magnetic measurements, Iron and steel products, Graphical symbols, Semiconductor devices, Electrical wires and cables, Measurement of volume, mass, density, viscosity, Screw threads, Components for electrical equipment, Kitchen equipment, Integrated circuits. Microelectronics, Installations in buildings, Paints and varnishes, Pharmaceutics, Rectifiers. Convertors. Stabilized power supply, Bearings, Veterinary medicine, Mechanical structures for electronic equipment, Construction industry, Optoelectronics. Laser equipment, Bridge construction, Farming and forestry, Wastes, Radiation protection, Protection against dangerous goods, Paint ingredients, Quality, Insulating fluids, Thermodynamics and temperature measurements, Measurement of fluid flow.

Group Standards of the People's Republic of China, In vitro/be

T/SCDA 083-2021 BE insulation and decoration composite board exterior wall insulation system building structure
T/CECS 10104-2020 Insulated decorative panel for external wall of building
T/NAHIEM 36-2021 In-vitro diagnostic management (distribution) enterprise group standards
T/HIS 002-2022 Silicon-based infrared gas sensor
T/CNMIA 0031-2021 Cardiopulmonary bypass process management practices
T/HIS 013-2022 Pyroelectric infrared gas sensor
T/SZJCH 0003-2022 General Technical Requirements for Cellular Exosomes
T/CSTM 00316-2022 Optoelectric single crystals - Lithium tantalate single crystals for pyroelectric infrared detection
T/JXBMIF 001-2022 ZY silicon-aluminum foam insulation and decoration integrated board external wall external insulation building structure
T/JSSIA 0008-2021 Outline Dimensions of Package on Package Lower Package
T/SHMHZQ 003-2022 General requirements for exosome extraction kits
T/CNMIA 0030-2021 Establish procedures for extracorporeal circulation
T/JSSIA 0007-2021 Outline Dimensions of Package on Package Upper Package
T/JSSES 11-2020 External Regenerated Alumina Carrier Catalyst
T/WSJD 43-2023 Thyroid 131I measurement technique in vitro
T/ZHCA 009-2019 Method of skin irritation test in vitro for face cream cosmetic products-In vitro skin irritation test with reconstructed skin model
T/CECS 1313-2023 Inorganic substrate coated decorative surface integrated panel exterior wall external thermal insulation engineering technical regulations
T/CSBM 0003-2021 Additive manufacturing of titanium alloy acetabular cup for surgical implant total hip prosthesis
T/SHSYCXH 7-2022 Test method of human monocyte populations from peripheral blood-Flow cytometry
T/SHDSGY 026-2023 Disposable blood extracorporeal circulation tubing
T/ZMDS 40001-2021 Guidelines for values assignment of calibrator of IVD
T/ZHCA 013-2021 Method of eye irritation test in vitro for facial cleanser cosmetic products - In vitro eye irritation test with reconstructed human cornea-like epithelial model

Korean Agency for Technology and Standards (KATS), In vitro/be

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 6122-1991 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)
KS V 0023-2001 Glossary of terms for shipbuilding(Hull part-outfittings)
KS V 0023-1986 Glossary of terms for shipbuilding(Hull part-outfittings)
KS C 3134-2008(2018) Contact conductors with insulating covers
KS B 50117-2005(2020) Measuring systems for liquids other than water
KS P ISO 15676:2018 Cardiovascular implants and artificial organs — Requirements for single-use tubing packs for cardiopulmonary bypass(CPB) and extracorporeal membrane oxygenation(ECMO)
KS I 2217-2009 Non-dispersive infrared gas analyzer
KS M 5957-2022 Paint, oil, exterior concrete and masonary
KS P 1800-2019 Protocol for evaluation of matrix effects in in-vitro diagnostic test
KS P ISO 23317:2009 Implants for surgery-In vitro evaluation for apatite-forming ability of implant materials
KS P 2093-2020 In-vitro degradation test of absorbable metals
KS P SIO 18113-2-2012 In vitro diagnostic medical devices--Information supplied by the manufacturer (labelling)--Part 2：In vitro diagnostic reagents for professional use
KS P ISO 18113-4-2015(2020) In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 4: In vitro diagnostic reagents for self-testing
KS F 4920-2004 Liquid-applied compounds forwaterproofing membrane coating of exterior wall
KS P ISO 8871:2008 Elastomeric parts for aqueous parenteral preparations
KS P ISO 8871:2004 Elastomeric parts for aqueous parenteral preparations
KS P ISO 18113-2:2018 In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 2: In vitro diagnostic reagents for professional use
KS P ISO 18113-3-2015(2020) In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
KS P ISO 18113-5-2015(2020) In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 5: In vitro diagnostic instruments for self-testing
KS P ISO 9583-2009(2019) Implants for surgery－Non-destructive testing－Liquid penetrant inspection of metallic surgical implants
KS B ISO 4053-1-2001(2011) Measurement of gas flow in conduits－Tracer method－Part 1：General

American National Standards Institute （ANSI), In vitro/be

ANSI/EIA 417-A:1991 Crystal Outlines
ANSI/AWWA C710-2009 Cold-Water Meters - Displacement Type, Plastic Main Case
ANSI/AWWA C700-2009 Cold-Water Meters - Displacement Type, Bronze Main Case
ANSI/AAMI/ISO 11658:2012 Cardiovascular implants and extracorporeal systems - Blood/tissue contact surface modifications for extracorporeal perfusion systems

National Metrological Verification Regulations of the People's Republic of China, In vitro/be

JJG(电子) 04019-1988 BJ2902 type bipolar transistor H_21E, V (subscript BE (sat)), V (subscript CE (sat)) standard instrument trial verification regulations
JJG 1181-2021 γ Radiation Sources Used in Body Stereotactic Radiation Therapy

British Standards Institution (BSI), In vitro/be

BS DD CEN/TS 15411:2006 Solid recovered fuels - Methods for the determination of the content of trace elements (As, Ba, Be, Cd, Co, Cr, Cu, Hg, Mo, Mn, Ni, Pb, Sb, Se, Tl, V and Zn)
DD CEN/TS 15411:2006 Solid recovered fuels — Methods for the determination of the content of trace elements (As, Ba, Be, Cd, Co, Cr, Cu, Hg, Mo, Mn, Ni, Pb, Sb, Se, Tl, V and Zn)
BS EN 15411:2011 Solid recovered fuels. Methods for the determination of the content of trace elements (As, Ba, Be, Cd, Co, Cr, Cu, Hg, Mo, Mn, Ni, Pb, Sb, Se, Tl, V and Zn)
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 Tracked Changes. In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
BS EN 62134-1:2002 Fibre optic enclosures - Generic specification
BS EN 62134-1:2010 Fibre optic interconnecting devices and passive components. Fibre optic closures. Generic specification
BS EN ISO 22523:2006 External limb prostheses and external orthoses - Requirements and test methods
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 ISO 24443:2012 Determination of sunscreen UVA photoprotection in vitro
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 18113-3:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for professional use
BS EN ISO 18113-5:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for self-testing
PD CEN/TS 17747:2022 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood. DNA, RNA and proteins
BS 7313-1.2:1990 Prosthetics and orthotics - Glossary of terms relating to external limb prostheses and wearers of external limb prostheses
BS EN ISO 18113-2:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic reagents for professional use
BS ISO 11658:2012 Cardiovascular implants and extracorporeal systems. Blood/tissue contact surface modifications for extracorporeal perfusion systems
BS EN ISO 2812-1:2007 Paints and varnishes - Determination of resistance to liquids - Immersion in liquids other than water
BS ISO 8637-3:2018 Extracorporeal systems for blood purification. Plasmafilters
BS ISO 23317:2009 Implants for surgery. In vitro evaluation for apatite-forming ability of implant materials
BS ISO 23317:2012 Implants for surgery. In vitro evaluation for apatite-forming ability of implant materials
BS ISO 23317:2014 Implants for surgery. In vitro evaluation for apatite-forming ability of implant materials
BS EN 13640:2002 Stability testing of in vitro diagnostic reagents
BS ISO 17593:2022 Clinical laboratory testing and in vitro medical devices. Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
20/30424657 DC BS EN ISO 6717. In vitro diagnostic medical devices. Single-use containers for the collection of specimens, other than blood, from humans
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 EN 1658:1997 Requirements for marking of in vitro diagnostic instruments
22/30419490 DC BS EN ISO 22523. External limb prostheses and external orthoses. Requirements and test methods
PD ISO/TR 21624:2020 Nanotechnologies. Considerations for in vitro studies of airborne nano‐objects and their aggregates and agglomerates (NOAA)

Association Francaise de Normalisation, In vitro/be

NF X34-225*NF EN 15411:2011 Solid recovered fuels - Methods for the determination of the content of trace elements (As, Ba, Be, Cd, Co, Cr, Cu, Hg, Mo, Mn, Ni, Pb, Sb, Se, Tl, V and Zn).
NF EN 15411:2011 Combustibles solides de récupération - Méthodes de détermination de la teneur en éléments à l'état de traces (As, Ba, Be, Cd, Co, Cr, Cu, Hg, Mo, Mn, Ni, Pb, Sb, Se, Tl, V et Zn)
NF S90-550:1986 Medico-surgical equipment. External breast prostheses.
NF EN ISO 23640:2015 Dispositifs médicaux de diagnostic in vitro - Évaluation de la stabilité des réactifs de diagnostic in vitro
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 S92-017:1995 IN VITRO DIAGNOSTIC SYSTEMS. REQUIREMENTS FOR USER MANUALS FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR HOME USE. (EUROPEAN STANDARD EN 592).
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 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).
NF S96-800*NF EN ISO 22523:2006 External limb prostheses and external orthoses - Requirements and test methods
NF S90-448:1990 Medico-surgical equipment. Implants for surgery. Hip joint prostheses. Static breaking test of femoral rods.
NF E03-615*NF ISO 2901:2016 ISO metric trapezoidal screw threads. Basic profile and maximum material profiles.
NF E03-615:1997 ISO metric trapezoidal screw threads. Basic profile and maximum material profiles.
NF S92-036:2004 In vitro diagnostic medical devices - Single-use receptables for the collection of specimens, other than blood, from humans.
NF S92-036*NF EN ISO 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood
NF S94-090:2005 Medico-surgical equipment - Materials for ancillary positioning instruments for surgical instrument - Martensitic, precipitation hardening, austenitic and austeno-ferritic stainless steels.
NF S92-031:1996 In vitro diagnostic systems. Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for in vitro diagnostic medical devices.
NF EN ISO 19001:2013 Dispositifs médicaux de diagnostic in vitro - Informations fournies par le fabricant avec les réactifs de coloration de diagnostic in vitro utilisés en biologie
NF S92-010-4:2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4 : in vitro diagnostic reagents for self-testing.
NF S92-010-5:2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5 : in vitro diagnostic instruments for self-testing.
NF S92-010-4*NF EN ISO 18113-4:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4 : in vitro diagnostic reagents for self-testing
NF S92-010-5*NF EN ISO 18113-5:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5 : in vitro diagnostic instruments for self-testing
NF EN 14136:2004 Utilisation des programmes d'évaluation externe de la qualité dans l'évaluation de la performances des procédures de diagnostic in vitro
NF S92-032:2002 Stability testing of in vitro diagnostic reagents.
NF EN 13612:2002 Évaluation des performances des dispositifs médicaux de diagnostic in vitro
NF EN ISO 24443:2021 Cosmétiques - Détermination in vitro de la photoprotection UVA
NF S92-010-2:2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2 : in vitro diagnostic reagents for professional use.
NF S92-010-3:2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3 : in vitro diagnostic instruments for professional use.
NF S92-010-3*NF EN ISO 18113-3:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3 : in vitro diagnostic instruments for professional use
NF EN ISO 18113-3:2012 Dispositifs médicaux de diagnostic in vitro - Informations fournies par le fabricant (étiquetage) - Partie 3 : instruments de diagnostic in vitro à usage professionnel
NF EN ISO 18113-2:2012 Dispositifs médicaux de diagnostic in vitro - Informations fournies par le fabricant (étiquetage) - Partie 2 : réactifs de diagnostic in vitro à usage professionnel
NF C93-476-2:2000 Mechanical structures for electronic equipment - Outdoor enclosures - Part 2 : sectional specification - Coordination dimensions for cases and cabinets.
NF ISO 104:2016 Roulements - Butées - Dimensions d'encombrement, plan général
NF S92-010-2*NF EN ISO 18113-2:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2 : in vitro diagnostic reagents for professional use
NF EN ISO 18113-5:2012 Dispositifs médicaux de diagnostic in vitro - Informations fournies par le fabricant (étiquetage) - Partie 5 : instruments de diagnostic in vitro pour auto-tests
NF EN ISO 18113-4:2012 Dispositifs médicaux de diagnostic in vitro - Informations fournies par le fabricant (étiquetage) - Partie 4 : réactifs de diagnostic in vitro pour auto-tests

RU-GOST R, In vitro/be

GOST R ISO 23640-2015 In vitro medical devices. Evaluation of stability of in vitro diagnostic reagents
GOST R ISO 8549-1-2011 Prosthetics and orthotics. Vocabulary. Part 1. General terms for external limb prostheses and external orthoses
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 51352-2013 In vitro diagnostic medical devices. Test methods
GOST R ISO 18113-5-2015 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 5. In vitro diagnostic instruments for self-testing
GOST R ISO 18113-3-2015 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 3. In vitro diagnostic instruments for professional use
GOST R ISO 18113-4-2015 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 4. In vitro diagnostic reagents for self-testing
GOST R ISO 18113-2-2015 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 2. In vitro diagnostic reagents for professional use
GOST R ISO 13781-2011 Poly(L-lactide) resins and fabricated forms for surgical implants. In vitro degradation testing

HU-MSZT, In vitro/be

Military Standards (MIL-STD), In vitro/be

DOD A-A-53263-1988 ADHESIVE LIQUID, SURGICAL (AEROSOL)

US-FCR, In vitro/be

FCR FED FCGS 02711-1979 OUTSIDE GAS SYSTEM
FCR FED H-08-3 403-1-1987 OUTSIDE GAS DISTRIBUTION
FCR NAV GSH 15.9 REVISION 1-1967 GAS DISTRIBUTION SYSTEM, EXTERIOR
FCR COE 15.9 REVISION 1-1967 GAS DISTRIBUTION SYSTEM, EXTERIOR
FCR NAV GSH 15.9-1966 GAS DISTRIBUTION SYSTEM, EXTERIOR
FCR COE 15.9-1966 GAS DISTRIBUTION SYSTEM, EXTERIOR
FCR AF M85-25 SEC 15.9-1966 GAS DISTRIBUTION SYSTEM, EXTERIOR
FCR 21 CFR PART 809-2015 IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
FCR 21 CFR PART 809-2013 IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE

Japanese Industrial Standards Committee (JISC), In vitro/be

JIS T 3248:2022 Extracorporeal blood circuit
JIS T 3248:2005 Extracorporeal blood circuit
JIS T 3248:2011 Extracorporeal blood circuit
JIS T 3248:2012 Extracorporeal blood circuit
JIS T 1356:1989 External cardiac pacemaker
JIS K 0151:1983 Non-dispersive infrared gas analyzer
JIS B 1559:1995 Rolling bearings -- Cast and pressed housings for insert bearings

European Committee for Standardization (CEN), In vitro/be

EN 15411:2011 Solid recovered fuels - Methods for the determination of the content of trace elements (As, Ba, Be, Cd, Co, Cr, Cu, Hg, Mo, Mn, Ni, Pb, Sb, Se, Tl, V and Zn)
EN ISO 23640:2013 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
EN ISO 23640:2011 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents [Superseded: CEN EN 13640]
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)
EN 12376:1999 In Vitro Diagnostic Medical Devices - Information Supplied by the Manufacturer with in Vitro Diagnostic Reagents for Staining in Biology
EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
prEN 928-1992 In vitro diagnostic systems; guidance on the application of EN 29001/EN 46001 and EN 29002/EN 46002 for the in vitro diagnostics industry
FprCEN/TS 17747-2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins
prCEN ISO/TS 18702 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins
CEN/TS 17747:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins
EN ISO 22523:2006 External limb prostheses and external orthoses - Requirements and test methods (ISO 22523:2006)
EN ISO 18113-5:2011 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
EN ISO 24443:2021 Cosmetics - Determination of sunscreen UVA photoprotection in vitro (ISO 24443:2021, Corrected version 2022-02)
EN ISO 24443:2012 Determination of sunscreen UVA photoprotection in vitro
CEN EN 13640-2002 Stability Testing of in Vitro Diagnostic Reagents
EN ISO 18113-2:2011 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
EN 928:1995 In Vitro Diagnostic Systems - Guidance on the Application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for in Vitro Diagnostic Medical Devices

CEN - European Committee for Standardization, In vitro/be

PD CEN/TS 15411:2006 Solid recovered fuels - Methods for the determination of the content of trace elements (As@ Ba@ Be@ Cd@ Co@ Cr@ Cu@ Hg@ Mo@ Mn@ Ni@ Pb@ Sb@ Se@ Tl@ V and Zn)
EN ISO 18113-2:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use

Danish Standards Foundation, In vitro/be

DS/EN 15411:2011 Solid recovered fuels - Methods for the determination of the content of trace elements (As, Ba, Be, Cd, Co, Cr, Cu, Hg, Mo, Mn, Ni, Pb, Sb, Se, Tl, V and Zn)
DS/EN 376:1993 In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testing
DS/EN 375:1993 In vitro diagnostic systems. Requirements for labelling of in vitro diagnostic reagents for professional use
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
DS/ISO 6717:2021 In vitro diagnostic medical devices – Single-use containers for the collection of specimens from humans other than blood
DS/EN ISO 24443:2012 Determination of sunscreen UVA photoprotection in vitro
DS/EN ISO 19001:2013 In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology

Lithuanian Standards Office , In vitro/be

LST EN 15411-2011 Solid recovered fuels - Methods for the determination of the content of trace elements (As, Ba, Be, Cd, Co, Cr, Cu, Hg, Mo, Mn, Ni, Pb, Sb, Se, Tl, V and Zn)

AENOR, In vitro/be

UNE-EN 15411:2012 Solid recovered fuels - Methods for the determination of the content of trace elements (As, Ba, Be, Cd, Co, Cr, Cu, Hg, Mo, Mn, Ni, Pb, Sb, Se, Tl, V and Zn)
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)
UNE-EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices.
UNE-EN 14136:2004 Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures

German Institute for Standardization, In vitro/be

DIN EN 15411:2011-11 Solid recovered fuels - Methods for the determination of the content of trace elements (As, Ba, Be, Cd, Co, Cr, Cu, Hg, Mo, Mn, Ni, Pb, Sb, Se, Tl, V and Zn); German version EN 15411:2011
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 ISO 22523:2007-04 External limb prostheses and external orthoses - Requirements and test methods (ISO 22523:2006); English version of DIN EN ISO 22523:2007-04
DIN EN 15411:2011 Solid recovered fuels - Methods for the determination of the content of trace elements (As, Ba, Be, Cd, Co, Cr, Cu, Hg, Mo, Mn, Ni, Pb, Sb, Se, Tl, V and Zn); German version EN 15411:2011
DIN EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans; German version EN 14254:2004
DIN CEN/TS 17747:2022-08 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins; German version CEN/TS 17747:2022
DIN EN ISO 6717:2020 In vitro diagnostic medical devices - Single-use containers for the collection of specimens, other than blood, from humans (ISO/DIS 6717:2020); German and English version prEN ISO 6717:2020
DIN 41814-2:1976 Cases for semiconductor devices; cases type 160 to 168, main dimensions
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 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011); German version EN ISO 23640:2011
DIN EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011); German version EN ISO 23640:2015
DIN EN ISO 23640:2013 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 6717:2021-12 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021); German version EN ISO 6717:2021
DIN 41885:1976 Cases type 101 for semiconductor devices; main dimensions

AT-ON, In vitro/be

ONORM EN 376-1993 In vitro diagnostic Systems - Requirements for labelling of in vitro diagnostic reagents for serf-testing
ONORM EN 375-1993 In vitro diagnostic Systems - Requirements for labelling of in vitro diagnostic reagents for professional use
ONORM M 6316-1999 Rolling bearings - General plan of boundary dimensions

KR-KS, In vitro/be

KS P ISO 23640-2019 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
KS P ISO 22523-2016 External limb prostheses and external orthoses — Requirements and test methods
KS P ISO 15676-2018 Cardiovascular implants and artificial organs — Requirements for single-use tubing packs for cardiopulmonary bypass(CPB) and extracorporeal membrane oxygenation(ECMO)
KS P ISO 13960-2017 Cardiovascular implants and extracorporeal systems — Plasmafilters
KS P ISO 8871-2004 Elastomeric parts for aqueous parenteral preparations
KS P ISO 18113-2-2018 In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 2: In vitro diagnostic reagents for professional use

International Organization for Standardization (ISO), In vitro/be

ISO 23640:2011 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
ISO/CD 3884:2023 Solid recovered fuels — Methods for the determination of the content of elements (Al, Ca, Fe, K, Mg, Na, P, S, Si, Ti, As, Ba, Be, Cd, Co, Cr, Cu, Hg, Mo, Mn, Ni, Pb, Sb, Se, Sn, Tl, V, Zn)
ISO 8549-1:2020 Prosthetics and orthotics — Vocabulary — Part 1: General terms for external limb prostheses and external orthoses
ISO 18113-4:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing
ISO 23317:2007 Implants for surgery - In vitro evaluation for apatite-forming ability of implant materials
ISO 13781:1997 Poly(L-lactide) resins and fabricated forms for surgical implants - In vitro degradation testing
ISO/CD 23317 Implants for surgery — In vitro evaluation for apatite-forming ability of implant materials
ISO 23317:2012 Implants for surgery - In vitro evaluation for apatite-forming ability of implant materials
ISO 23317:2014 Implants for surgery - In vitro evaluation for apatite-forming ability of implant materials
ISO 8871:1988 Elastomeric parts for aqueous parenteral preparations
ISO 18113-5:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing
ISO 18113-3:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use
ISO 18113-4:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing
ISO 18113-3:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
ISO 18113-5:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing
ISO 18113-2:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use
ISO 15814:1999 Implants for surgery - Copolymers and blends based on polylactide - In vitro degradation testing
ISO 11658:2012 Cardiovascular implants and extracorporeal systems - Blood/tissue contact surface modifications for extracorporeal perfusion systems
ISO 18113-2:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use
ISO 9583:1993 Implants for surgery; non-destructive testing; liquid penetrant inspection of metallic surgical implants

ES-UNE, In vitro/be

UNE-EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
UNE-EN ISO 6717:2022 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)
UNE-CEN/TS 17747:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins (Endorsed by Asociación Española de Normalización in June of 2022.)
UNE-EN 13612/AC:2003 Performance evaluation of in vitro diagnostic medical devices.

国家药品监督管理局, In vitro/be

YY/T 1579-2018 In vitro diagnostic medical devices and in vitro diagnostic reagent stability evaluation

BE-NBN, In vitro/be

NBN EN 592-1995 In vitro diagnostic systems - Requirements for user manual for in vitro diagnostic instruments for home use
NBN EN 591-1995 In vitro diagnostic systems - Requirements for user manuals for in vitro diagnostic instruments for professional use
NBN-EN 376-1992 In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for self-testing
NBN 736-1970
NBN C 66-101-1976
NBN C 66-102-1976

YU-JUS, In vitro/be

JUS M.A5.013-1991 Cone. Methods for testing of internat and external cones
JUS N.R9.071-1986 Piezoelectric vibrators. Quartz crystal units. Two mre crystal holder outline, type 18
JUS N.R9.070-1986 Piezoelectric vibrators. Ouartz crystal units. Two pin crystal holder outlfne, type09
JUS N.R9.073-1986 Piezoelectrlc vibrators. Quartz crystal unlts. Two wire crystal holder outline, type 17
JUS N.R9.069-1986 Piezoelectric vibrators. Quartz crystal units. Two piri crystal holder outline, type 07

ES-AENOR, In vitro/be

UNE 48 078

U.S. Military Regulations and Norms, In vitro/be

ARMY MIL-B-50762 NOTICE 1-1997 BODY ASSEMBLY IR, 11743800
ARMY MIL-B-50762-1972 BODY ASSEMBLY IR, 11743800
ARMY MIL-PRF-44156 E-2006 KITCHEN, COMPANY LEVEL, FIELD FEEDING (KCLFF), COMPONENTS THEREOF

AIA/NAS - Aerospace Industries Association of America Inc., In vitro/be

NASM25087-1999 Screw@ Externally Relieved Body
NASM25087-2011 SCREW@ EXTERNALLY RELIEVED BODY (Rev 1)

US-CFR-file, In vitro/be

CFR 15-801.8-2014 Commerce and Foreign Trade. Part801:Survey of international trade in services between u.s. and foreign persons and surveys of direct investment. Section801.8:Requirements for the BE–10, Benchmark Survey of U.S. Direct Investment Abroad-2014.
CFR 48-225.7003-3-2014 Federal Acquisition Regulations System. Part225:Foreign acquisition. Section225.7003-3:Exceptions.
CFR 48-225.772-4-2014 Federal Acquisition Regulations System. Part225:Foreign acquisition. Section225.070-4:Exception.

Professional Standard - Medicine, In vitro/be

YY/T 1434-2016 Medical devices for human in vitro assisted reproductive technology.In vitro mouse embryo assay
YY/T 1244-2014 Purified water for in vitro diagnostic reagents
YY 1048-2007 Artificial heart-lung machine.Extracorporeal blood circuit
YY/T 1153-2009 DNA microarray for in vitro diagnostics
YY/T 0639-2008 In vitro diagnostic medical devices.Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
YY/T 1447-2016 Implants for surgery.In vitro evaluation for apatite-forming ability of implant materials
YY/T 0473-2004 Implants for surgery-Copolymers and blends based on polylactide-In vitro degradation testing
YY 0001-2008 Technical requirements of equipment for extracorporeally induced lithotripsy
YY/T 0001-2008 Technical requirements of equipment for extracorporeally induced lithotripsy
YY 1048-2016 Cardiopulmonary bypass system extracorporeal circulation tubing
YY/T 0474-2004 Poly(L-lactide) resins and fabricated forms for surgical implants-In vitro degradation testing
YY/T 0690-2008 Clinical laboratory testing and in vitro medical devices -- Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
YY/T 1227-2014 In vitro diagnostic reagent (kit) nomenclature for clinical chemistry
YY/T 0343-2002 Liquid penetrant inspection of metallic surgical implants
YY/T 1151-2009 Protein microarray for in vitro diagnostics
YY 0267-1995 Extracorporeal blood circuit for blood purification devices

Taiwan Provincial Standard of the People's Republic of China, In vitro/be

CNS 12510-1989 Non-dispersed Infrared Gas Analyzer
CNS 6809-1989 Outlines Drawing Methods for Transistors
CNS 15042-2007 Standard specification for infrared thermometers for intermittent determination of patient temperature

Professional Standard - Hygiene , In vitro/be

WS/T 252-2005 Labeling of In Vitro Diagnosis Products

Professional Standard - Business, In vitro/be

SB/T 10917-2012 Washing device for inside & outside of poultry carcass

Professional Standard - Agriculture, In vitro/be

NY/T 3401-2018 Poultry carcass washing machine
270药典一部-2015 In vitro culture of bezoar
270药典一部-2020 In vitro culture of bezoar
270药典一部-2010 Medicinal materials and decoction pieces seven pictures in vitro culture of bezoar
162药典三部-2015 Monograph Ⅳ In Vitro Diagnosis Treponema pallidum Antibody Diagnostic Kit (Enzyme-linked Immunoassay)
183药典三部-2020 Monograph Ⅳ In Vitro Diagnosis Treponema pallidum Antibody Diagnostic Kit (Enzyme-linked Immunoassay)

国家市场监督管理总局、中国国家标准化管理委员会, In vitro/be

GB/T 38137-2019 Guidelines for in vitro screening of nucleic acid aptamers
GB/T 7092-2021 Outline dimensions of semiconductor integrated circuits

(U.S.) Joint Electron Device Engineering Council Soild State Technology Association, In vitro/be

JEDEC JESD22-B118-2011 Semiconductor Wafer and Die Backside External Visual Inspection

SE-SIS, In vitro/be

SIS 03 15 22-1976 Marking for sports and outdoor activities
SIS 03 12 11-1976 Graphic symbols for sports and outdoor activities

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, In vitro/be

GB 10035-1994 The alr-bag type sequential external counter-pulsation device
GB 10035-2006 Air-bag type sequential external counter-pulsation device
GB/T 14191.1-2009 Prosthestics and orthotics.Vocabulary.Part 1:General terms for external limb prostheses and external orthoses
GB/T 30827-2014 Technical conditions for external prestressing tendons
GB/T 7092-1993 Qutline dimensions of semiconductor integrated circuits
GB/T 26124-2011 In vitro diagnostic reagent(kit) for clinical chemistry
GB 10035-2017(英文版) Air bag type sequential external counter pulsation device
GB/T 7581-1987 Dimensions of outlines for semiconductor discrete devices
GB/T 3108-1999 Impressed current cathodic protection system for ship hull
GB/T 13971-1992 Specification of ultra-violet gas analyzers
GB/T 13971-2013 Specification of ultraviolet gas analyzers
GB/T 25929-2010 Specification of infrared gas analyzers
GB/T 25930-2010 Test method of infrared gas analyzers
GB/T 29791.3-2013 In vitro diagnostic medical devices.Information supplied by the manufacturer (labelling).Part 3:In vitro diagnostic instruments for professional use
GB/T 29791.4-2013 In vitro diagnostic medical devices.Information supplied by the manufacturer (labelling).Part 4:In vitro diagnostic reagents for selftesting
GB/T 29791.5-2013 In vitro diagnostic medical devices.Information supplied by the manufacturer (labelling).Part 5:In vitro diagnostic instruments for selftesting
GB/T 29791.2-2013 In vitro diagnostic medical devices.Information supplied by the manufacturer (labelling).Part 2:In vitro diagnostic reagents for professional use
GB/T 27830-2011 Chemicals.Test method of in vitro skin corrosion.Human skin model test
GB/T 18448.1-2001 Laboratory animal--Methods for examination of ectoparasites
GB/T 27818-2011 Chemicals.Testing method for skin absorption.In vitro
GB/T 14142-1993 Test method for sheet resistance of silicon epitaxial, diffused and ion-implanted layers using a collinear four-probe array
GB/T 19146-2010 Infrared devices for instant screening of human skin temperature
GB/T 21794-2008 Chemicals.Test method of in vitro mammalian chromosome aberration

中华人民共和国国家质量监督检验检疫总局、中国国家标准化管理委员会, In vitro/be

GB 10035-2017 Air-bag type sequential external counter-pulsation device

Aerospace Industries Association/ANSI Aerospace Standards, In vitro/be

AIA/NAS NASM25087-2011 SCREW, EXTERNALLY RELIEVED BODY

Heilongjiang Provincial Standard of the People's Republic of China, In vitro/be

DB23/ 1167-2013 HS-ICF technical specification for building energy-saving system with external wall insulation
DB23/T 1960-2017 Calf In Vitro Embryo Production Technical Regulations

Electronic Components, Assemblies and Materials Association, In vitro/be

ECA EIA-364-83-1999 TP-83 SHELL-TO-SHELL AND SHELL-TOBULKHEAD RESISTANCE TEST PROCEDURE FOR ELECTRICAL CONNECTORS

CZ-CSN, In vitro/be

CSN 06 0215-1961 Calculation of infrared radiator heating
CSN 63 1504-1992 Tyres. Determination of outer diameter and overall width of tyres

FI-SFS, In vitro/be

SFS 4276-1978

United States Navy, In vitro/be

NAVY MIL-STD-2100-1979 PROPELLANT, SOLID, CHARACTERIZATION OF (EXCEPT GUN PROPELLANT)

Aerospace Industries Association, In vitro/be

AIA NASM25087-1999 Screw, Externally Relieved Body FSC 5305

Society of Automotive Engineers (SAE), In vitro/be

SAE AS17184-2001 SCREW, EXTERNALLY RELIEVED BODY (SYNCHRO)
SAE AS17184A-2007 SCREW, EXTERNALLY RELIEVED BODY, CRES - (SYNCHRO)

SAE - SAE International, In vitro/be

SAE AS17184-1997 Screw@ Externally Relieved Body (Synchro)

Professional Standard - Machinery, In vitro/be

JB/T 11622-2013 Non-dispersive infrared gas sensor
JB/T 11937-2014 Portable infrared gas analyzer
JB/T 8175-1999 Outline dimensions of extruded heat sink for power semiconductor devices
JB/T 9359.1-1999 Specification of infrared gas analyzers
JB/T 9359.2-1999 Test method of infrared gas analyzers
JB/T 5631-1991 Epitaxial furnace for semiconductor devices. Energy efficiency standard

Professional Standard - Electron, In vitro/be

SJ/T 11247-2001 Tolerance and physical imperfections of permanent ferrite tegular magnets
SJ 2247-1982 Outlines dimension for semiconductor optoelectronic devices
SJ 2750-1987 Outline dimensions for semiconductor laser diodes

Indonesia Standards, In vitro/be

SNI 05-2062-1990 Metric trapezoidal screw threads. Basic profile and maximum material profiles

RO-ASRO, In vitro/be

STAS 3734-1971 Ovci'lH'iid power linos ZTNC-COATFD STRFJ. CONDUC- TOR S

American Water Works Association (AWWA), In vitro/be

AWWA C700-2009 Cold-Water Meters桪isplacement Type, Bronze Main Case
AWWA C710-2009 Cold-Water Meters桪isplacement Type, Plastic Main Case

Defense Logistics Agency, In vitro/be

DLA MS51495 VALID NOTICE 4-2008 Screw, Externally Relieved Body, Fillister Head

IETF - Internet Engineering Task Force, In vitro/be

RFC 4251-2006 The Secure Shell (SSH) Protocol Architecture
RFC 2017-1996 Definition of the URL MIME External-Body Access-Type

机械工业部, In vitro/be

JB/T 6306-1992 Power semiconductor module dimensions

Professional Standard - Commodity Inspection, In vitro/be

SN/T 2245-2009 Chemicals.In vitro skin corrosion.Human skin model test

Hubei Provincial Standard of the People's Republic of China, In vitro/be

DB42/T 1110-2015 In vitro drug susceptibility testing procedures for Mycoplasma bovis

国家药监局, In vitro/be

YY/T 0639-2019 In vitro diagnostic medical devices.Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
YY/T 1746-2020 Test method for breaking strength of absorbable surgical sutures after in vitro hydrolysis
YY/T 1808-2021 In vitro skin irritation test for medical devices

未注明发布机构, In vitro/be

DIN EN 14252:2004 In-vitro diagnostics – disposable vessels for human specimens with the exception of blood samples; German version EN 14254:2004
DIN EN 591:2001 Instructions for use for in vitro diagnostic instruments for professional use

Professional Standard - Aerospace, In vitro/be

QJ 1368-1988 External pressure test method for solid rocket motor combustor casing

VDI - Verein Deutscher Ingenieure, In vitro/be

VDI 2631-1968 PRUeFEN VON INNEN- UND AUssENKEGEL; PRUeEFMETHODE UND PRUeF- MITTEL

Military Standard of the People's Republic of China-General Armament Department, In vitro/be

GJB 8190-2015 General specification for semiconductor solid-state light sources for aircraft exterior lighting
GJB 1420A-1999 General Specification for Semiconductor Integrated Circuit Enclosures
GJB 1420B-2011 General specification for packages of semiconductor integrated circuits
GJB 923A-2004 General specification for packages of semiconductor discrete devices
GJB 923B-2021 General Specification for Semiconductor Discrete Device Enclosures

American Society for Testing and Materials (ASTM), In vitro/be

ASTM E2680-09e1 Standard Test Method for Appearance of Clear, Transparent Liquids (Visual Inspection Procedure)

AR-IRAM, In vitro/be

Professional Standard - Traffic, In vitro/be

JT/T 853-2013 External prestressing tendons of unbonded steel strand
JT/T 4402.16-1993 Hull Repair Technology Requires Appearance Quality

GM North America, In vitro/be

GM GM9327P-1999 Exterior Weatherability of Integrally Colored Plastics
GM GMP.E/P.016-2002 Thermoplastic Elastomer Polyolefinic, Shore D50, Interior/Exterior, Integrally Colored
GM GMP.E/P.120-2002 Thermoplastic Elastomer Polyolefinic, Shore A80, Interior/Exterior, Integrally Colored

IN-BIS, In vitro/be

IS 5000 OD.15-1973
IS 5000 OD.16-1973
IS 5000 OD.30-1981
IS 5000 OB.1-1969
IS 5000 OB.5-1969
IS 5000 OB.2-1969
IS 5000 OB.6-1969
IS 5000 OB.7-1969
IS 5000 OB.4-1969
IS 5000 OD.4-1969
IS 5000 OD.7-1969
IS 5000 OD.9-1969
IS 5000 OD.1-1969
IS 5000 OD.6-1969
IS 5000 OD.2-1969
IS 5000 OD.5-1969
IS 5000 OD.8-1969
IS 5000 OD.31-1981
IS 5000 OD.13-1971
IS 5000 OD.19-1974
IS 5000 OD.12-1971
IS 5000 OD.18-1974
IS 5000 OD.14-1971
IS 5000 OD.33-1981
IS 5000 OD.10-1971
IS 5000 OD.17-1974
IS 5000 OD.35-1981
IS 5000 OD.11-1971
IS 5000 OD.21-1979
IS 5000 OD.23-1978
IS 5000 OD.28-1978
IS 5000 OD.20-1978
IS 5000 OD.26-1978
IS 5000 OD.27-1978
IS 5000 OD.22-1978
IS 5000 OD.25-1978
IS 5000 OD.24-1979
IS 5000 OD.29-1979
IS 5000 OD.36-1981

U.S. Air-Conditioning, Heating, and Refrigeration Institute (US-AHRI), In vitro/be

ARI 270-2008 Sound Performance Rating of Outdoor Unitary Equipment

U.S. Air-Conditioning, Heating, and Refrigeration Institute (US-AHRI), In vitro/be

AHRI 270-2008 Sound Performance Rating of Outdoor Unitary Equipment

GOSTR, In vitro/be

GOST R EN 13612-2010 Performance evaluation of in vitro diagnostic medical devices
GOST R EN 592-2010 Instructions for use for in vitro diagnostic instruments for self-testing

Hebei Provincial Standard of the People's Republic of China, In vitro/be

DB13/T 2989-2019 Technical regulations for body shape and appearance identification of breeding pigs
DB13/T 2051-2014 Technical regulations for in vitro embryo production of young lambs

Professional Standard-Ships, In vitro/be

CB 907-1994 External thread bronze right angle liquid safety valve
CB/T 3377-2015 The degree of quality for high pressure water cleaning shell plate
CB 3377-1991 High pressure water cleaning quality grade of hull plating

Professional Standard - Aquaculture, In vitro/be

SC/T 8131-1994 Appearance quality requirements of fishing boat hull welds

CH-SNV, In vitro/be

SN EN ISO 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)

National Aeronautics and Space Administration (NASA), In vitro/be

NASA NPD 1370.1-2007 Reimbursable Utilization of NASA Facilities by Foreign Entities and Foreign-Sponsored Research

Professional Standard - Chemical Industry, In vitro/be

HG/T 4652-2014 Dyestuffs and intermediate of dyes.Outward appearance appraising

Professional Standard - Building Materials, In vitro/be

JC/T 439-1991 Zinc sulfide crystal intended to be used in the window of infrared detectors

Professional Standard - Pharmaceutical Packaging, In vitro/be

YBB 0039-2003 Waiyongyeti Yaoyong Gaomidujuyixi Ping HDPE Bottles for external use

Xinjiang Provincial Standard of the People's Republic of China, In vitro/be

DB65/T 3805-2015 Technical regulations for the physical appearance assessment of speed trotters
DB65/T 3806-2015 Technical regulations for assessment of physique and appearance of dairy horses

工业和信息化部, In vitro/be

JC/T 439-2021 Zinc sulfide crystals for infrared detector windows

Yunnan Provincial Standard of the People's Republic of China, In vitro/be

DB53/T 447.5-2022 Yunling Cattle Part 5: In vitro embryo production

API - American Petroleum Institute, In vitro/be

API PUBL 28-30726-1981 IN VIVO AND IN VITRO MUTAGENICITY STUDIES FLUID PROCESS COKE Sample 6-1-468