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Database: 365,228(8 Aug 2026)

plant exosomes

plant exosomes, Total:401 items.

The international standard classification for "plant exosomes" includes: Implants for surgery, prosthetics and orthotics , Stainless steels .

The Chinese standard classification for "plant exosomes" includes: Orthopedic devices , Medical apparatus and devices in general , Steel and iron products in general , Extracorporeal circulation, artificial organ and prosthesis device .


Group Standards of the People's Republic of China

  • T/GDMDMA 0023-2022 Vaginal secretion analyzer
  • T/QGCML 4542-2024 Exosome storage tank sealing tester
  • T/CSBM 0030-2023 Implants for Surgery—beta-tricalcium phosphate powder for additive manufacturing
  • T/LNSI 010-2024 Human amniotic mesenchymal stem cell derived exosomes
  • T/SZJCH 0003-2022 General Technical Requirements for Cellular Exosomes
  • T/GDMRS 001-2023 Implant for surgery—Total hip joint prostheses—Additive manufacturing titanium alloy femoral stems
  • T/CSBM 0003-2021 Additive manufacturing of titanium alloy acetabular cup for surgical implant total hip prosthesis
  • T/GDAAV 1011-2024 Implant for surgery–Technical specifications for veterinary hip-joint replacement implants
  • T/SHMHZQ 003-2022 General requirements for exosome extraction kits
  • T/CSBM 0028-2022 Tetracalcium phosphate for surgical implantation
  • T/CEAC 045-2024 Technical requirements for the application of stem cell exosomes in skin anti-aging
  • T/LNSI 011-2024 Human amniotic epithelial stem cell derived exosomes
  • T/SBIAORG 001-2023 Criteria for quality control of exosomes from mesenchymal stem cells
  • T/CEAC 057-2024 Technical Specifications for Stem Cell Exosome Drug Delivery
  • T/FDSA 0049-2024 Specifications: Production and Testing of Exosomes Derived from Human Mesenchymal Stem Cells

Professional Standard - Medicine

  • YY/T 0340-2002 Implants for surgery--Fundamental principles
  • YY/T 0919-2014 Non-active surgical implants―Joint replacement implants―Specific requirements for knee-joint replacement implants
  • YY 0117.2-1993 Implants for surger-Forgings castings for bone joint prostheses - ZTiAl5V4 titanium alloy castings
  • YY 0117.1-2005 Implants for surgery - Forgings, castings for bone joint prostheses - Ti6Al4V titanium alloy forgings
  • YY/T 0474-2004 Poly(L-lactide) resins and fabricated forms for surgical implants -
  • YY/T 0682-2008 Implants for surgery - Minimum data sets for surgical implants
  • YY/T 0343-2002 Liquid penetrant inspection of metallic surgical implants
  • YY/T 1447-2016 Implants for surgery—In vitro evaluation for apatite-forming ability of implant materials
  • YY 0647-2008 Non-active surgical implants - Mammary implants - Particular requirements
  • YY/T 1565-2017 Implants for surgery-Non-destructive testing-Radiographic examination of cast metallic surgical implants
  • YY/T 0473-2004 Implants for surgery - Copolymers and blends based on polylactide -
  • YY 0117.1-1993 Implants for surgery - Forgings, castings for bone joint prostheses - TC4 titanium alloy forgings
  • YY/T 0920-2014 Non-active surgical implants―Joint replacement implants―Specific requirements for hip-joint replacement implants
  • YY 0117.2-2005 Implants for surgery-Forgings, castings for bone joint prostheses-ZTi6Al4V titanium alloy castings
  • YY/T 0340-2009 Implants for surgery Fundamental principles

Taiwan Provincial Standard of the People's Republic of China

  • 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 13382.4-2004 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 13382-4-2004 Implants for surgery - Metallic materials - Wrought cobalt-nickel-chromium-molybdenum 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
  • CNS 13382.5-2004 Implants for surgery - Metallic materials - Unalloyed titanium
  • CNS 13382.1-2004 Implants for surgery - Metallic materials - Wrought stainless steel

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

  • GB/T 25440.2-2010 Retrieval and analysis of surgical implants—Part 2:Analysis of retrieved metallic surgical implants
  • GB/T 24629-2009 Implants for surgery—Guidance on care and handling of orthopaedic implants
  • GB 4234-1994 Stainless steel for surgical implants
  • GB/T 25440.3-2010 Retrieval and analysis of surgical implants—Part 3:Analysis of retrieved polymeric surgical implants
  • GB 4234-2003 Stainless steel for surgical implants

Professional Standard - Agriculture

  • 554药典 化学药和生物制品卷-2010 Chapter 7 Urinary System Drugs Section 3 Special Urinary System Drugs 1. Drugs for the treatment of benign prostatic hyperplasia (3) Natural herbal medicine Pushitai Tablets
  • 555药典 化学药和生物制品卷-2010 Chapter Seven Urinary System Drugs Section Three Urinary System Special Drugs 1. Drugs for the treatment of benign prostatic hyperplasia (3) Natural herbal medicine Pygeum africanum extract*

国家药监局

  • YY/T 0647-2021 Non-active surgical implants-Particular requirements of mammary implants

国家市场监督管理总局、中国国家标准化管理委员会

  • GB/T 25440.2-2021 Retrieval and analysis of surgical implants—Part 2:Analysis of retrieved surgical implants

Professional Standard - Commodity Inspection

Inner Mongolia Provincial Standard of the People's Republic of China

HU-MSZT

SCC

  • BS 3531-16:1985 Surgical implants-Specification for surgical implants made of heat-vulcanized silicone elastomer
  • DANSK DS/ISO 9583:2015 Implants for surgery - Non-destructive testing - Liquid penetrant inspection of metallic surgical implants
  • NS-EN 12180:2000 Non-active surgical implants — Body contouring implants — Specific requirements for mammary implants
  • 11/30217696 DC BS ISO 23317. Implants for surgery. In vitro evaluation for apatite-forming ability of implant materials
  • DANSK DS/ISO/TS 17137:2019 Cardiovascular implants and extracorporeal systems – Cardiovascular absorbable implants
  • BS PD ISO/TS 17137:2019 Cardiovascular implants and extracorporeal systems. Cardiovascular absorbable implants
  • DANSK DS/EN ISO 21535:2009 Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants
  • DANSK DS/EN ISO 21536:2009 Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants
  • DANSK DS/EN ISO 21536/A1:2009 Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants
  • DANSK DS/EN ISO 21535/A1:2009 Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants
  • BS 3531-2:1980 Surgical implants-Specification for materials for metal surgical implants
  • 06/30151792 DC BS ISO 23317. Implants for surgery. In vitro measurement for apatite-forming ability of implant materials
  • 06/30143888 DC ISO 21536. Non-active surgical implants. Joint replacement implants. Specific requirements for knee-joint replacement implants
  • 06/30143831 DC ISO 21535. Non-active surgical implants. Joint replacement implants. Specific requirements for hip-joint replacement implants
  • AAMI/ISO 7198:2016 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches
  • NS-EN ISO 21535:2007 Non-active surgical implants — Joint replacement implants — Specific requirements for hip-joint replacement implants (ISO 21535:2007)
  • NS-EN ISO 21536:2009 Non-active surgical implants — Joint replacement implants — Specific requirements for knee-joint replacement implants (ISO 21536:2007)
  • NS-EN ISO 21536:2007 Non-active surgical implants — Joint replacement implants — Specific requirements for knee-joint replacement implants (ISO 21536:2007)
  • DANSK DS/ISO 18242:2016 Cardiovascular implants and extracorporeal systems – Centrifugal blood pumps
  • BS 3531-13:1983 Surgical implants-Specification for bearing surfaces of hip joint prostheses
  • DANSK DS/ISO 18242/AMD 1:2016 Cardiovascular implants and extracorporeal systems – Centrifugal blood pumps
  • DANSK DS/EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems – Vascular prostheses – Tubular vascular grafts and vascular patches (ISO 7198:2016)
  • NS-EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems — Vascular prostheses — Tubular vascular grafts and vascular patches (ISO 7198:2016)
  • BS 3531-17:1985 Surgical implants-Recommendations for the care and handling of orthopaedic surgical implants
  • AENOR UNE-EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches (ISO 7198:2016)
  • DIN EN ISO 21535 E:2021 Draft Document – Non-active surgical implants – Joint replacement implants – Specific requirements for hip-joint replacement implants (ISO/DIS 21535:2021); German and English version prEN ISO 21535:2021
  • DIN EN ISO 21536 E:2021 Draft Document – Non-active surgical implants – Joint replacement implants – Specific requirements for knee-joint replacement implants (ISO/DIS 21536:2021); German and English version prEN ISO 21536:2021
  • DANSK DS/EN ISO 14607:2009 Non-active surgical implants – Mammary implants – Particular requirements
  • DANSK DS/ISO 18193:2021 Cardiovascular implants and artificial organs – Cannulae for extracorporeal circulation
  • DANSK DS/ISO 13960:2015 Cardiovascular implants and extracorporeal systems – Plasmafilters
  • DIN EN ISO 7198 E:2014 Draft Document - Cardiovascular implants and extracorporeal systems - Vascular Prostheses - Tubular vascular grafts and vascular patches (ISO/DIS 7198:2014); German version prEN ISO 7198:2014
  • DANSK DS/EN ISO 14602:2011 Non-active surgical implants - Implants for osteosynthesis - Particular requirements
  • BS ISO 23317:2007 Implants for surgery. In vitro evaluation for apatite-forming ability of implant materials
  • DANSK DS/ISO/TS 12417:2011 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products
  • AAMI/ISO TIR12417:2011 Cardiovascular implants and extracorporeal systems -- Vascular device-drug combination products
  • BS 3531-12:1982 Surgical implants-Classification and designation of dimensions for knee joint prostheses
  • DANSK DS/EN ISO 21534:2009 Non-active surgical implants - Joint replacement implants - Particular requirements
  • DANSK DS/ISO 13781:2017 Implants for surgery – Homopolymers, copolymers and blends on poly(lactide) – In vitro degradation testing
  • DANSK DS/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
  • SN-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 3531-1:1968 Specification for metal implants and toos used in bone surgery. Materials for metal surgical implants
  • BS 3531-22:1988 Surgical implants-Recommendations for retrieval and examination of orthopaedic surgical implants and associated tissues
  • AAMI/ISO 11658:2012 Cardiovascular implants and extracorporeal systems - Blood/tissue contact surface modifications for extracorporeal perfusion systems
  • 12/30217461 DC BS ISO 16087. Implants for surgery. Roentgen stereophotogrammetry for assessment of micromotion of orthopaedic implants
  • DANSK DS/ISO 11658:2014 Cardiovascular implants and extracorporeal systems - Blood/tissue contact surface modifications for extracorporeal perfusion systems
  • NS-EN ISO 14607:2007 Non-active surgical implants — Mammary implants — Particular requirements (ISO 14607:2007)
  • 11/30197571 DC BS ISO 25832-1. Implants for surgery. Seamless tubes for surgical implants. Part 1. Materials based on iron
  • DANSK DS/ISO 12891-3:2000 Retrieval and analysis of surgical implants - Part 3: Analysis of retrieved polymeric surgical implants
  • NS-EN ISO 14607:2009 Non-active surgical implants — Mammary implants — Particular requirements (ISO 14607:2007)
  • NS-EN 12010:1998 Non-active surgical implants — Joint replacement implants — Particular requirements
  • BS EN ISO 16054:2002 Implants for surgery. Minimum data sets for surgical implants
  • AWWA MTC64596 Membrane Adsorption of Endocrine Disrupting Compounds and Pharmaceuticals
  • NS-EN 12563:1998 Non-active surgical implants — Joint replacement implants — Specific requirements for hip joint replacement implants
  • NS-EN ISO 14602:2009 Non-active surgical implants - Implants for Osteosynthesis - Particular requirements (ISO 14602:1998)
  • BS 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

European Committee for Standardization (CEN)

  • EN 12180:2000 Non-Active Surgical Implants - Body Contouring Implants - Specific Requirements for Mammary Implants
  • EN ISO 16054:2019 Implants for surgery - Minimum data sets for surgical implants (ISO 16054:2019)
  • EN ISO 16054:2002 Implants for surgery - Minimum data sets for surgical implants ISO 16054: 2000
  • EN ISO 5840-2:2021 Cardiovascular implants - Cardiac valve prostheses - Part 2: Surgically implanted heart valve substitutes (ISO 5840-2:2021)
  • EN ISO 5840-2:2015 Cardiovascular implants - Cardiac valve prostheses - Part 2: Surgically implanted heart valve substitutes (ISO 5840-2:2015)
  • EN ISO 14607:2018 Non-active surgical implants - Mammary implants - Particular requirements
  • EN ISO 14607:2009 Non-active surgical implants - Mammary implants - Particular requirements (ISO 14607:2007)
  • EN ISO 14602:2009 Non-active surgical implants - Implants for Osteosynthesis - Particular requirements
  • EN ISO 14602:2010 Non-active surgical implants - Implants for osteosynthesis - Particular requirements
  • EN ISO 14602:2011 Non-active surgical implants - Implants for osteosynthesis - Particular requirements (ISO 14602:2010)
  • 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 21534:2009 Non-active surgical implants - Joint replacement implants - Particular requirements
  • EN 12564:1998 Non-Active Surgical Implants - Joint Replacement Implants - Specific Requirements for Knee Joint Replacement Implants Ratified European Text

International Organization for Standardization (ISO)

  • ISO 5840:1984 Implants for surgery — Cardiovascular implants — Cardiac valve prostheses
  • ISO/CD 14607 Non-active surgical implants — Mammary implants — Specific requirements
  • ISO 9583:1993 Implants for surgery; non-destructive testing; liquid penetrant inspection of metallic surgical implants
  • ISO 12417-1:2024 Cardiovascular implants and extracorporeal systems
  • ISO/FDIS 5910:2023 Cardiovascular implants and extracorporeal systems
  • 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 23317:2007 Implants for surgery - In vitro evaluation for apatite-forming ability of implant materials
  • ISO/CD 23317 Implants for surgery — In vitro evaluation for apatite-forming ability of implant materials
  • ISO/TS 17137:2019 Cardiovascular implants and extracorporeal systems — Cardiovascular absorbable implants
  • ISO/TS 17137:2014 Cardiovascular implants and extracorporeal systems - Cardiovascular absorbable implants
  • ISO/TS 17137:2021 Cardiovascular implants and extracorporeal systems - Cardiovascular absorbable implants
  • ISO 16054:2000 Implants for surgery - Minimum data sets for surgical implants
  • ISO 15814:1999 Implants for surgery - Copolymers and blends based on polylactide - In vitro degradation testing
  • ISO 16087:2013 Implants for surgery.Roentgen stereophotogrammetric analysis for the assessment of migration of orthopaedic implants
  • ISO 13781:2017 Implants for surgery - Homopolymers, copolymers and blends on poly(lactide) - In vitro degradation testing
  • ISO 19227:2018 Implants for surgery - Cleanliness of orthopedic implants - General requirements
  • ISO 7198:2016 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches
  • ISO/FDIS 7197:2024 Neurosurgical implants
  • ISO 14607:2002 Implants for surgery - Specific requirements for mammary implants
  • ISO/DIS 14607:2023 Non-active surgical implants — Mammary implants — Specific requirements
  • ISO 5840-2:2021 Cardiovascular implants - Cardiac valve prostheses - Part 2: Surgically implanted heart valve substitutes
  • ISO 5840-2:2015 Cardiovascular implants - Cardiac valve prostheses - Part 2: Surgically implanted heart valve substitutes
  • ISO 13781:1997 Poly(L-lactide) resins and fabricated forms for surgical implants - In vitro degradation testing
  • ISO/FDIS 14607:2024 Non-active surgical implants — Mammary implants — Specific requirements
  • ISO 13782:1996 Implants for surgery - Metallic materials - Unalloyed tantalum for surgical implant applications
  • ISO 18242:2016 Cardiovascular implants and extracorporeal systems - Centrifugal blood pumps
  • ISO 14607:2007 Non-active surgical implants - Mammary implants - Particular requirements
  • ISO 14607:2018 Non-active surgical implants - Mammary implants - Particular requirements
  • ISO/TS 12417:2011 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products
  • ISO 9584:1993 Implants for surgery; non-destructive testing; radiographic examination of cast metallic surgical implants
  • ISO 18193:2021 Cardiovascular implants and artificial organs — Cannulae for extracorporeal circulation
  • ISO 16672:2003 Ophthalmic implants - Ocular endotamponades
  • ISO 8828:1988 Implants for surgery; guidance on care and handling of orthopaedic implants
  • ISO 12891-1:2011 Implants for surgery - Retrieval and analysis of surgical implants - Part 1: Retrieval and handling
  • ISO 14602:1998 Non-active surgical implants - Implants for Osteosynthesis - Particular requirements
  • ISO 14602:2010 Non-active surgical implants - Implants for osteosynthesis - Particular requirements
  • ISO 8828:2014 Implants for surgery - Guidance on care and handling of orthopaedic implants
  • ISO/TR 14283:2004 Implants for surgery - Fundamental principles
  • ISO/TR 14283:1995 Implants for surgery - Fundamental principles
  • ISO 16672:2015 Ophthalmic implants - Ocular endotamponades
  • ISO/DIS 9584.2 Implants for surgery — Non-destructive testing — Radiographic examination of cast metallic surgical implants
  • ISO 12891-2:2014 Retrieval and analysis of surgical implants - Part 2: Analysis of retrieved surgical implants
  • ISO 12891-2:2020 Retrieval and analysis of surgical implants — Part 2: Analysis of retrieved surgical implants
  • ISO 21534:2007 Non-active surgical implants - Joint replacement implants - Particular requirements
  • ISO 5910:2018 Cardiovascular implants and extracorporeal systems - Cardiac valve repair devices
  • ISO/DIS 5910 Cardiovascular implants and extracorporeal systems — Cardiac valve repair devices
  • ISO 21536:2007 Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants
  • ISO 21535:2007 Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants

Korean Agency for Technology and Standards (KATS)

  • KS P ISO 9583-2009(2019) Implants for surgery-Non-destructive testing-Liquid penetrant inspection of metallic surgical implants
  • KS P ISO 9583:2009 Implants for surgery-Non-destructive testing-Liquid penetrant inspection of metallic surgical implants
  • KS P ISO 23317:2009 Implants for surgery-In vitro evaluation for apatite-forming ability of implant materials
  • KS P ISO 16054-2009(2019) Implants for surgery-Minimum data sets for surgical implants
  • KS P ISO 21536:2020 Non-active surgical implants — Joint replacement implants — Specific requirements for knee-joint replacement implants
  • KS P ISO 16054:2009 Implants for surgery-Minimum data sets for surgical implants
  • KS P ISO 7198:2018 Cardiovascular implants and extracorporeal systems — Vascular prostheses — Tubular vascular grafts and vascular patches
  • KS P ISO 15814-2008(2013) Implants for surgery-Copolymers and blends based on polylactide-In vitro degradation testing
  • KS P ISO 15814:2008 Implants for surgery-Copolymers and blends based on polylactide-In vitro degradation testing
  • KS P ISO 13782:2021 Implants for surgery — Metallic materials — Unalloyed tantalum for surgical implant applications
  • KS P ISO 13782-2009(2019) Implants for surgery-Metallic materials-Unalloyed tantalum for surgical implant applications
  • KS P ISO 23317:2020 Implants for surgery — In vitro evaluation for apatite-forming ability of implant materials
  • KS P ISO 18242-2023 Cardiovascular implants and extracorporeal systems — Centrifugal blood pumps
  • KS P ISO 18242:2018 Cardiovascular implants and extracorporeal systems — Centrifugal blood pumps
  • KS P ISO 13781:2019 Implants for surgery — Homopolymers, copolymers and blends on poly(lactide) — In vitro degradation testing
  • KS P ISO 14949:2009 Implants for surgery-Two-part addition-cure silicone elastomers
  • KS P ISO 13782:2009 Implants for surgery-Metallic materials-Unalloyed tantalum for surgical implant applications
  • KS P ISO 13960-2022 Cardiovascular implants and extracorporeal systems — Plasmafilters
  • KS P ISO 14602-2022 Non-active surgical implants-Implants for osteosynthesis-Particular requirements
  • KS P ISO 14607:2020 Non-active surgical implants — Mammary implants — Particular requirements
  • KS P ISO 14602:2017 Non-active surgical implants-Implants for osteosynthesis-Particular requirements
  • KS P ISO 14607:2009 Implants for surgery-Specific requirements for mammary implants
  • 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 14602:2010 Non-N surgical implants-Implants for osteosynthesis-Particular requirements
  • KS P ISO 21534-2019 Non-active surgical implants-Joint replacement implants-Particular requirements
  • KS P ISO TR 14283:2009 Implants for surgery-Fundamental principles
  • KS P ISO 16672:2006 Ophthalmic implants-Ocular endotamponades
  • KS P ISO 9584-2009(2019) Implants for surgery-Non-destructive testing-Radiographic examination of cast metallic surgical implants
  • KS P ISO 12891-3-2019 Retrieval and analysis of surgical implants-Part 3:Analysis of retrieved polymeric surgical implants
  • KS P ISO 9584:2009 Implants for surgery-Non-destructive testing-Radiographic examination of cast metallic surgical implants
  • KS P ISO 12891-2:2019 Retrieval and analysis of surgical implants — Part 2: Analysis of retrieved surgical implants
  • KS P ISO TS 23810:2020 Cardiovascular implants and artificial organs — Checklists for use of extracorporeal circulation equipment
  • KS P ISO 21535:2010 Non-active surgical implants-Joint replacement implants-Specific requirements for hip-joint replacement implants
  • KS P ISO 12891-3-2008(2013) Retrieval and analysis of surgical implants-Part 3:Analysis of retrieved polymeric surgical implants
  • KS P ISO 15814-2019 Implants for surgery-Copolymers and blends based on polylactide-In vitro degradation testing
  • KS P ISO 21534-2009(2019) Non-active surgical implants-Joint replacement implants-Particular requirements

United States Navy

British Standards Institution (BSI)

  • BS ISO 23317:2009 Implants for surgery. In vitro evaluation for apatite-forming ability of implant materials
  • BS EN 12180:2000 Non-Active Surgical Implants - Body Contouring Implants - Specific Requirements for Mammary Implants
  • 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
  • PD ISO/TS 17137:2021 Cardiovascular implants and extracorporeal systems. Cardiovascular absorbable implants
  • BS PD ISO/TS 17137:2014 Cardiovascular implants and extracorporeal systems. Cardiovascular absorbable implants
  • BS PD ISO/TS 17137:2021 Cardiovascular implants and extracorporeal systems. Cardiovascular absorbable implants
  • BS EN ISO 16054:2001 Implants for surgery. Minimum data sets for surgical implants
  • BS ISO 16054:2001 Implants for surgery - Minimum data sets for surgical implants
  • BS EN ISO 5840-2:2015 Cardiovascular implants. Cardiac valve prostheses. Surgically implanted heart valve substitutes
  • BS EN ISO 5840-2:2021 Cardiovascular implants. Cardiac valve prostheses. Surgically implanted heart valve substitutes
  • BS 7253-3:1990 Non-metallic materials for surgical implants - Specification for surgical implants made of heat-vulcanized silicone elastomer
  • BS ISO 16087:2013 Implants for surgery. Roentgen stereophotogrammetric analysis for the assessment of migration of orthopaedic implants
  • BS ISO 13781:2017 Implants for surgery. Homopolymers, copolymers and blends on poly(lactide). In vitro degradation testing
  • BS ISO 18242:2016+A1:2023 Cardiovascular implants and extracorporeal systems. Centrifugal blood pumps
  • BS ISO 12891-1:2011 Implants for surgery. Retrieval and analysis of surgical implants. Retrieval and handling
  • BS ISO 12891-2:2014 Retrieval and analysis of surgical implants. Analysis of retrieved surgical implants
  • BS 7730:1994 Method for liquid penetrant inspection of metallic surgical implants
  • BS EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems. Vascular prostheses. Tubular vascular grafts and vascular patches
  • BS ISO 14949:2001 Implants for surgery - Two-part addition-cure silicone elastomers
  • BS ISO 18193:2021 Cardiovascular implants and artificial organs. Cannulae for extracorporeal circulation
  • BS ISO 18242:2016 Cardiovascular implants and extracorporeal systems. Centrifugal blood pumps
  • BS EN ISO 14607:2008 Non-active surgical implants - Mammary implants - Particular requirements
  • BS EN ISO 14607:2007 Non-active surgical implants - Mammary implants - Particular requirements
  • BS EN ISO 14607:2009 Non-active surgical implants - Mammary implants - Particular requirements
  • BS DD ISO/TS 12417:2011 Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products
  • BS ISO 14243-2:2010 Implants for surgery. Wear of total knee-joint prostheses. Methods of measurement
  • BS EN ISO 21534:2009 Non-active surgical implants - Joint replacement implants - Particular requirements
  • 15/30275224 DC BS ISO 18242. Cardiovascular implants and extracorporeal systems. Centrifugal blood pumps
  • BS EN ISO 14602:1998 Non-active surgical implants - Implants for osteosynthesis - Particular requirements
  • BS ISO 8828:2014 Implants for surgery. Guidance on care and handling of orthopaedic implants
  • BS EN ISO 14602:2010 Non-active surgical implants - Implants for osteosynthesis - Particular requirements
  • BS ISO 14243-2:2009 Implants for surgery - Wear of total knee-joint prostheses - Methods of measurement
  • BS EN ISO 14602:2011 Non-active surgical implants. Implants for osteosynthesis. Particular requirements
  • BS 7252-13:1997 Metallic materials for surgical implants. Specification for unalloyed tantalum for surgical implant applications
  • BS EN 12010:1998 Non-active surgical implants - Joint replacement implants - Particular requirements
  • BS EN 12006-3:1998+A1:2009 Non active surgical implants - Particular requirements for cardiac and vascular implants - Endovascular devices
  • 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 EN ISO 16054:2019 Implants for surgery. Minimum data sets for surgical implants
  • 21/30439465 DC BS ISO 18242 AMD1. Cardiovascular implants and extracorporeal systems. Centrifugal blood pumps
  • BS EN 12006-3+A1:1999 Non active surgical implants. Particular requirements for cardiac and vascular implants. Endovascular devices
  • BS EN ISO 21536:2009+A1:2014 Non-active surgical implants. Joint replacement implants. Specific requirements for knee-joint replacement implants
  • BS EN ISO 21536:2009 Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants
  • BS ISO 23089-2:2021 Implants for surgery. Pre-clinical mechanical assessment of spinal implants and particular requirements. Spinal intervertebral body fusion devices
  • BS ISO 5910:2024 Cardiovascular implants and extracorporeal systems. Cardiac valve repair devices
  • BS ISO 5910:2018 Cardiovascular implants and extracorporeal systems. Cardiac valve repair devices
  • BS EN 12564:1999 Non-Active Surgical Implants - Joint Replacement Implants - Specific Requirements for Knee Joint Replacement Implants Ratified European Text
  • BS EN ISO 21535:2024 Non-active surgical implants. Joint replacement implants. Specific requirements for hip-joint replacement implants
  • BS EN 125:2010+A1:2015 Non-Active Surgical Implants - Joint Replacement Implants - Specific Requirements for Knee Joint Replacement Implants Ratified European Text

GSO

  • OS GSO ISO 23317:2015 Implants for surgery -- In vitro evaluation for apatite-forming ability of implant materials
  • OS GSO ISO/TS 17137:2015 Cardiovascular implants and extracorporeal systems -- Cardiovascular absorbable implants
  • GSO ISO 21535:2015 Non-active surgical implants -- Joint replacement implants -- Specific requirements for hip-joint replacement implants
  • OS GSO ISO 21536:2015 Non-active surgical implants -- Joint replacement implants -- Specific requirements for knee-joint replacement implants
  • BH GSO ISO 21536:2017 Non-active surgical implants -- Joint replacement implants -- Specific requirements for knee-joint replacement implants
  • BH GSO ISO 21535:2017 Non-active surgical implants -- Joint replacement implants -- Specific requirements for hip-joint replacement implants
  • OS GSO ISO 21535:2015 Non-active surgical implants -- Joint replacement implants -- Specific requirements for hip-joint replacement implants
  • GSO ISO 16054:2015 Implants for surgery -- Minimum data sets for surgical implants
  • GSO ISO/TS 17137:2015 Cardiovascular implants and extracorporeal systems -- Cardiovascular absorbable implants
  • GSO ISO 18242:2021 Cardiovascular implants and extracorporeal systems — Centrifugal blood pumps
  • BH GSO ISO 18242:2022 Cardiovascular implants and extracorporeal systems — Centrifugal blood pumps
  • GSO ISO 14949:2015 Implants for surgery -- Two-part addition-cure silicone elastomers
  • GSO ISO 14607:2015 Non-active surgical implants -- Mammary implants -- Particular requirements
  • OS GSO ISO 14607:2015 Non-active surgical implants -- Mammary implants -- Particular requirements
  • BH GSO ISO 13782:2017 Implants for surgery -- Metallic materials -- Unalloyed tantalum for surgical implant applications
  • GSO ISO 13782:2015 Implants for surgery -- Metallic materials -- Unalloyed tantalum for surgical implant applications
  • BH GSO ISO 13960:2017 Cardiovascular implants and extracorporeal systems -- Plasmafilters
  • BH GSO ISO 14602:2017 Non-active surgical implants -- Implants for osteosynthesis -- Particular requirements
  • OS GSO ISO 13960:2015 Cardiovascular implants and extracorporeal systems -- Plasmafilters
  • GSO ISO 14602:2015 Non-active surgical implants -- Implants for osteosynthesis -- Particular requirements
  • GSO ISO 21534:2015 Non-active surgical implants -- Joint replacement implants -- Particular requirements
  • BH GSO ISO 21534:2017 Non-active surgical implants -- Joint replacement implants -- Particular requirements
  • OS GSO ISO 21534:2015 Non-active surgical implants -- Joint replacement implants -- Particular requirements
  • GSO ISO 12891-1:2015 Implants for surgery -- Retrieval and analysis of surgical implants -- Part 1: Retrieval and handling
  • GSO ISO 11658:2015 Cardiovascular implants and extracorporeal systems -- Blood/tissue contact surface modifications for extracorporeal perfusion systems
  • BH GSO ISO 11658:2017 Cardiovascular implants and extracorporeal systems -- Blood/tissue contact surface modifications for extracorporeal perfusion systems
  • ISO 5910:2024 Cardiovascular implants and extracorporeal systems — Cardiac valve repair devices
  • GSO ISO 13884:2014 Animal and vegetable fats and oils -- Determination of isolated trans isomers by infrared spectrometry
  • GSO ISO 21536:2015 Non-active surgical implants -- Joint replacement implants -- Specific requirements for knee-joint replacement implants
  • BH GSO ISO 13781:2017 Poly(L-lactide) resins and fabricated forms for surgical implants -- In vitro degradation testing

Danish Standards Foundation

  • DS/ISO/TS 17137:2021 Cardiovascular implants and extracorporeal systems – Cardiovascular absorbable implants
  • DS/EN ISO 16054:2002 Implants for surgery - Minimum data sets for surgical implants (ISO 16054:2000)
  • DS/ISO/TS 12417:2011 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products
  • DS/ISO 18193:2021 Cardiovascular implants and artificial organs – Cannulae for extracorporeal circulation

German Institute for Standardization

  • DIN EN ISO 21535:2021-08 Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants (ISO/DIS 21535:2021); German and English version prEN ISO 21535:2021 / Note: Date of issue 2021-07-16*Intended as replacement for DIN E...
  • DIN EN ISO 21536:2021-08 Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants (ISO/DIS 21536:2021); German and English version prEN ISO 21536:2021 / Note: Date of issue 2021-07-16*Intended as replacement for DIN ...
  • DIN EN ISO 21536:2009 Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants
  • DIN EN ISO 16054 E:2018-02 Surgical Implants Minimum Data Set for Surgical Implants (Draft)
  • DIN CEN/TS 15277:2006 Non-active surgical implants - Injectable implants; German version CEN/TS 15277:2006
  • DIN EN ISO 16054:2019 Implants for surgery - Minimum data sets for surgical implants (ISO 16054:2019)
  • DIN EN ISO 7198 E:2014-10 Cardiovascular Implants and Extracorporeal Systems Vascular Prostheses Tubular Vascular Grafts and Vascular Patches (Draft)
  • DIN EN ISO 7198:2017-07 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches (ISO 7198:2016); German version EN ISO 7198:2017 / Note: DIN EN 12006-2 (2009-08) remains valid alongside this standard until 2020-0...
  • DIN EN ISO 14607:2007 Non-active surgical implants - Mammary implants - Particular requirements (ISO 14607:2007); German version EN ISO 14607:2007
  • DIN EN ISO 14602:2012-06 Non-active surgical implants - Implants for osteosynthesis - Particular requirements (ISO 14602:2010); German version EN ISO 14602:2011
  • DIN EN ISO 14602:2012 Non-active surgical implants - Implants for osteosynthesis - Particular requirements (ISO 14602:2010); German version EN ISO 14602:2011
  • DIN EN ISO 21534:2009-08 Non-active surgical implants - Joint replacement implants - Particular requirements (ISO 21534:2007); German version EN ISO 21534:2009 / Note: DIN EN ISO 21534 (2007-12) remains valid alongside this standard until 2010-03-21.
  • DIN EN ISO 14607 E:2017-05 Passive Surgical Implants Breast Implant Specific Requirements (Draft)
  • DIN EN ISO 16672:2003 Ophthalmic implants - Ocular endotamponades (ISO 16672:2003); German version EN ISO 16672:2003
  • DIN EN ISO 21534:2007 Non-active surgical implants - Joint replacement implants - Particular requirements (ISO 21534:2007); German version EN ISO 21534:2007
  • DIN EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches (ISO 7198:2016); German version EN ISO 7198:2017
  • 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 58801:1972 Surgical implants; intramedullary nails type Küntscher
  • DIN EN ISO 16054:2002 Implants for surgery - Minimum data sets for surgical implants (ISO 16054:2000); German version EN ISO 16054:2002

KR-KS

  • KS P ISO 13960-2017 Cardiovascular implants and extracorporeal systems — Plasmafilters
  • KS P ISO 21536-2020 Non-active surgical implants — Joint replacement implants — Specific requirements for knee-joint replacement implants
  • KS P ISO 21535-2017 Non-active surgical implants — Joint replacement implants — Specific requirements for hip-joint replacement implants
  • KS P ISO 7198-2018 Cardiovascular implants and extracorporeal systems — Vascular prostheses — Tubular vascular grafts and vascular patches
  • KS P ISO 7198-2018(2023) Cardiovascular implants and extracorporeal systems — Vascular prostheses — Tubular vascular grafts and vascular patches
  • KS P ISO 13782-2021 Implants for surgery — Metallic materials — Unalloyed tantalum for surgical implant applications
  • KS P ISO 18242-2018 Cardiovascular implants and extracorporeal systems — Centrifugal blood pumps
  • KS P ISO 23317-2020 Implants for surgery — In vitro evaluation for apatite-forming ability of implant materials
  • KS P ISO 13781-2019 Implants for surgery — Homopolymers, copolymers and blends on poly(lactide) — In vitro degradation testing
  • KS P ISO 18242-2018(2023) Cardiovascular implants and extracorporeal systems — Centrifugal blood pumps
  • KS P ISO 14602-2017 Non-active surgical implants-Implants for osteosynthesis-Particular requirements
  • KS P ISO 14607-2020 Non-active surgical implants — Mammary implants — Particular requirements
  • 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 12891-2-2019 Retrieval and analysis of surgical implants — Part 2: Analysis of retrieved surgical implants
  • KS P ISO 14602-2017(2022) Non-active surgical implants-Implants for osteosynthesis-Particular requirements
  • KS P ISO TS 23810-2020 Cardiovascular implants and artificial organs — Checklists for use of extracorporeal circulation equipment

Association Francaise de Normalisation

  • NF EN ISO 21535:2009 Non-active surgical implants - Joint replacement implants - Specific requirements for hip joint replacement implants
  • NF EN ISO 21536:2009 Non-active surgical implants - Joint replacement implants - Specific requirements for knee joint replacement implants
  • NF S91-163:2000 Biofonctionnality of dental implants - In vitro tests.
  • NF EN ISO 16054:2019 Surgical implants - Minimum data sets for surgical implants
  • NF S94-103*NF EN ISO 16054:2019 Implants for surgery - Minimum data sets for surgical implants
  • NF S94-165*NF EN ISO 21535:2009 Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants
  • NF S94-103:2002 Implants for surgery - Minimum data sets for surgical implants.
  • NF EN ISO 7198:2017 Implants cardiovasculaires et systèmes extracorporels - Prothèses vasculaires - Greffons vasculaires tubulaires et pièces vasculaires
  • NF S94-204*NF EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems - Vascular Prostheses - Tubular vascular grafts and vascular patches
  • NF EN ISO 21536/A1:2014 Non-active surgical implants - Joint replacement implants - Specific requirements for knee joint replacement implants - Amendment 1
  • NF EN ISO 21535/A1:2017 Non-active surgical implants - Joint replacement implants - Specific requirements for hip joint replacement implants - Amendment 1
  • NF S90-437:1989 Implants for surgery. Guidance on care and handling of orthopaedic implants.
  • NF S94-165:2008 Non-active surgical implants - Joint replacement implants - Specific requirements for hip-joint replacement implants.
  • NF S90-480:1987 MEDICO-SURGICAL EQUIPMENT. IMPLANTS FOR SURGERY. CARDIOVASCULAR IMPLANTS. CARDIAC VALVE PROSTHESES.
  • NF S94-174:2008 Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants.
  • NF EN ISO 14607:2018 Implants chirurgicaux non actifs - Implants mammaires - Exigences particulières
  • NF S90-448:1990 Medico-surgical equipment. Implants for surgery. Hip joint prostheses. Static breaking test of femoral rods.
  • NF S94-350:2009 Non-active surgical implants - Mammary implants - Particular requirements.
  • NF S94-350:2007 Non-active surgical implants - Mammary implants - Particular requirements.
  • NF S94-101*NF EN ISO 14602:2012 Non-active surgical implants - Implants for osteosynthesis - Particular requirements
  • NF ISO 19227:2018 Implants chirurgicaux - Propreté des implants orthopédiques - Exigences générales
  • NF S94-091*NF ISO 19227:2018 Implants for surgery - Cleanliness of orthopedic implants - General Requirements
  • NF EN ISO 21534:2009 Non-active surgical implants - Joint replacement implants - Special requirements
  • NF S94-753:2003 Ophthalmic implants - Ocular endotamponades.
  • NF S94-753:2015 Ophthalmic implants - Ocular endotamponades
  • NF S94-753*NF EN ISO 16672:2021 Ophthalmic implants - Ocular endotamponades
  • NF S94-165:1999 Non-active surgical implants. Joint replacement implants. Specific requirements for hip joint replacement implants.
  • NF S94-164:1998 Non-active surgical implants. Joint replacement implants. Particular requirements.
  • NF S94-164*NF EN ISO 21534:2009 Non-active surgical implants - Joint replacement implants - Particular requirements.
  • NF S94-174:1999 Non-active surgical implants. Joint replacement implants. Specific requirements for knee joint replacement implants.
  • NF S94-164:2008 Non-active surgical implants - Joint replacement implants - Particular requirements.
  • NF S94-174*NF EN ISO 21536:2009 Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants
  • NF EN ISO 7199:2017 Implants cardiovasculaires et organes artificiels - Échangeurs gaz/sang extracorporels (oxygénateurs)

US-FCR

RU-GOST R

  • GOST R ISO 16054-2013 Implants for surgery. Minimum data sets for surgical implants
  • GOST 30399-1995 Implants for surgery. Metal bone screws with asymmetrical thrend and spherical under-surface. Mechanical requirements and test methods
  • GOST R ISO 13782-2017 Implants for surgery. Metallic materials. Unalloyed tantalum for surgical implant applications
  • GOST R ISO 14949-2014 Implants for surgery. Two-part addition-cure silicone elastomers
  • GOST R ISO 14607-2017 Non-active surgical implants. Mammary implants. Particular requirements
  • GOST R ISO 13781-2011 Poly(L-lactide) resins and fabricated forms for surgical implants. In vitro degradation testing
  • GOST R 57386-2017 Implants for surgery. Fundamental principles
  • GOST R ISO 14602-1999 Non-active surgical implants. Implants for osteosynthesis. Particular requirements
  • GOST R ISO 12891-3-2012 Retrieval and analysis of surgical implants. Part 3. Analysis of retrieved polymeric surgical implants
  • GOST R ISO 21534-2013 Non-active surgical implants. Joint replacement implants. Particular requirements
  • GOST R ISO 12891-2-2012 Retrieval and analysis of surgical implants. Part 2. Analysis of retrieved metallic surgical implants
  • GOST R ISO 21535-2013 Non-active surgical implants. Joint replacement implants. Specific requirements for hip-joint replacement implants

American National Standards Institute (ANSI)

  • ANSI/AAMI/ISO 7198:2016 Cardiovascular implants and extracorporeal systems— Vascular prostheses—Tubular vascular grafts and vascular patches
  • ANSI/AAMI/ISO 18242:2016 Cardiovascular implants and extracorporeal systems— Centrifugal blood pumps

Spanish Association for Standardization (UNE)

  • UNE-EN ISO 21536:2008 Non-active surgical implants - Joint replacement implants - Specific requirements for knee-joint replacement implants (ISO 21536:2007)
  • UNE-EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches (ISO 7198:2016)
  • UNE-EN 12180:2000 Non-active surgical implants. Body contouring implants. Specific requirements for mammary implants.
  • 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 ISO 14607:2007 Non-active surgical implants - Mammary implants - Particular requirements (ISO 14607:2007)
  • UNE-EN ISO 16054:2002 Implants for surgery. Minimum data sets for surgical implants. (ISO 16054:2000)
  • UNE-EN 12010:1998 NON-ACTIVE SURGICAL IMPLANTS. JOINT REPLACEMENT IMPLANTS. PARTICULAR REQUIREMENTS.
  • UNE-EN ISO 14602:2010 Non-active surgical implants - Implants for osteosynthesis - Particular requirements (ISO 14602:2010)

South African Bureau of Standard

Lithuanian Standards Office

PT-IPQ

  • NP EN ISO 14630:2000 Non-active surgical implants General requirements(ISO 14630:1997)
  • NP EN 12006-3-2000 Non active surgical implants Particular requirements for cardiac and vascular implants Part 3:Endovascular devices
  • NP EN 12010-2000 Non-active surgical implants Joint replacement implants Particular requirements

Standard Association of Australia (SAA)

RO-ASRO

  • STAS SR ISO 9583:1995 Implants for surgery. Non-destructive testing. Liquid penetrant inspection of metailic surgical implants

IN-BIS

  • IS 8079-1976 Operating table, surgery, urology specifications

YU-JUS

CEN - European Committee for Standardization

  • EN 12010:1998 Non-Active Surgical Implants - Joint Replacement Implants - Particular Requirements

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

  • AS/NZS 2817:1997 Implants for surgery - Care and handling of orthopaedic implants

VN-TCVN

  • TCVN 6796-2001 Implants for surgery.Guidance on care and handling of orthopaedic implants

TH-TISI

  • TIS 1684-1998 Implants for surgery.guidance on care and handling of orthopaedic implants