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Database: 365,228(8 Aug 2026)

organic blood vessels

organic blood vessels, Total:332 items.

The international standard classification for "organic blood vessels" includes: Implants for surgery, prosthetics and orthotics , Transfusion, infusion and injection equipment , Radiographic equipment , Medical Sciences and health care facilities in general .

The Chinese standard classification for "organic blood vessels" includes: Medical optical instrument and endoscope , General and microsurgical devices , Extracorporeal circulation, artificial organ and prosthesis device , Medical radiographic equipment , Medical science , Medical and foodstuff rubber products , Sanitation in general .


Professional Standard - Agriculture

国家药监局

  • YY/T 0663.1-2021 Cardiovascular implants—Endovascular devices—Part 1:Endovascular prostheses
  • YY/T 0500-2021 Cardiovascular implants and extracorporeal systems-vascular prostheses-tubular vascular grafts and vascular patches

未注明发布机构

Professional Standard - Medicine

  • YY/T 0754-2009 Particular requirements of the safety and essential performance for blood pressure transmission tubes for use with invasive blood pressure monitoring equipment
  • YY/T 0663.2-2024 Cardiovascular implantable devices Intravascular devices Part 2: Vascular stents
  • YY/T 0859-2011 Standard guide for finite element analysis(FEA) of metallic vascular stents subjected to uniform radial loading
  • YY/T 0663.1-2014 Cardiovascular implant―Endovascular devices―Part 1:Endovascular prostheses
  • YY/T0663.3-2016/ISO 25539-3:2011 Cardiovascular Implants Intravascular Devices Part 3: Vena Cava Filters
  • YY/T 0740-2022 Particular specifications for medical X-ray angiography equipment
  • YY/T 0740-2009 Particular specifications for medical X-ray angiography equipment
  • YY 0500-2004 Cardiovascular implants -- Tubular vascular prostheses
  • YY/T 1925-2024 Cardiovascular implants endovascular devices- Neurovascular stent retriev
  • YY/T 0031-1990 Silicone rubber infusion (blood) Tube
  • YY/T 0663.2-2016 Cardiovascular implants Endovascular devices-Part 2:Vascular stems

Shanghai Provincial Standard of the People's Republic of China

  • DB31/T 1335-2021 Management specificatinos for delivery of blood sample for transfusion and recycling disposition of post-transfusion blood bag in medical institutions

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

Jiangsu Provincial Standard of the People's Republic of China

  • DB32/T 3545.5-2023 Standards for blood purification therapy―Part 5:Code of practice of emergency procedure for blood purification center
  • DB32/T 3545.4-2021 Technical Management of Blood Purification Therapy Part 4: Medical Quality Management Standards for Blood Purification Medical Institutions
  • DB32/T 3545.1-2019 Technical management of blood purification therapy part 1 Infection management norms in blood purification therapy institutions

Professional Standard - Chemical Industry

Group Standards of the People's Republic of China

工业和信息化部

Tianjin Provincial Standard of the People's Republic of China

  • DB12/T 751-2017 Specifications for the construction of blood transfusion departments (blood banks) in medical institutions

国家食品药品监督管理局

  • YY/T 0663.3-2016 Cardiovascular implants-Endovascular devices-Part 3:Vena cava filters

Taiwan Provincial Standard of the People's Republic of China

  • CNS 14194-1998 Extracorporeal blood circuit for haemodialysers hasmofilters and haemoconcentrators

RO-ASRO

  • STAS 11326/8-1985 RUBBER STOPPERS FOR BLOOD, PLASMA AND INJECTABLE AND PERFUSABLE AQUEOUS SOLUTIONS Microbiological checking up of poisonous substances with antibacterian action
  • STAS 11327/9-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Organic substances determination

Association Francaise de Normalisation

  • NF B35-207:1969 LABORATORY GLASSWARE. HEMOLYSIS TUBES. KAHN TUBES SO-CALLED CENTRIFUGE HEMOLYSIS TUBES.
  • NF S94-201-2/IN1*NF EN 12006-2/IN1:2009 Non active surgical implants - Particular requirements for cardiac and vascular implants - Part 2 : vascular prostheses including cardiac valve conduits
  • 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 S94-203-2:2013 Cardiovascular implants - Endovascular devices - Part 2: vascular stents
  • NF S94-203-1:2008 Cardiovascular implants - Endovascular devices - Part 1 : endovascular prostheses.
  • NF EN ISO 25539-1:2018 Implants cardiovasculaires - Dispositifs endovasculaires - Partie 1 : prothèses endovasculaires
  • NF S94-203-1*NF EN ISO 25539-1:2018 Cardiovascular implants - Endovascular devices - Part 1 : endovascular prostheses
  • NF EN ISO 25539-2:2020 Implants cardiovasculaires - Dispositifs endovasculaires - Partie 2 : endoprothèses vasculaires
  • NF S94-203-1:2009 Cardiovascular implants - Endovascular devices - Part 1 : endovascular prostheses.
  • NF S97-532:2010 Health IT - Messages concerning blood transfusion - Message for distribution of labile blood products
  • NF S93-031-2:1997 Sterile, single-use intravascular catheters. Part 2 : angiographic catheters.
  • NF EN ISO 3826-3:2008 Soft plastic bags for blood and blood components - Part 3: Blood bag systems with integrated accessories
  • NF EN ISO 25539-3:2012 Implants cardiovasculaires - Dispositifs endovasculaires - Partie 3 : filtres caves
  • NF S93-302*NF EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • NF EN ISO 3826-4:2015 Soft plastic bags for blood and blood components - Part 4: Apheresis blood bag systems with integrated accessories
  • NF S94-203-3*NF EN ISO 25539-3:2012 Cardiovascular implants - Endovascular devices - Part 3 : vena cava filters

Japanese Industrial Standards Committee (JISC)

British Standards Institution (BSI)

  • BS EN ISO 25539-2:2020 Cardiovascular implants. Endovascular devices - Vascular stents
  • BS EN ISO 25539-2:2010 Cardiovascular implants. Endovascular devices. Vascular stents
  • BS EN ISO 25539-1:2017 Cardiovascular implants. Endovascular devices. Endovascular prostheses
  • BS EN ISO 25539-2:2012 Cardiovascular implants. Endovascular devices. Vascular stents
  • BS EN ISO 25539-2:2009 Cardiovascular implants - Endovascular devices - Vascular stents
  • BS EN ISO 25539-2:2008 Cardiovascular implants - Endovascular devices - Vascular stents
  • BS EN ISO 25539-1:2009 Cardiovascular implants - Endovascular devices - Endovascular prostheses
  • BS EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems. Vascular prostheses. Tubular vascular grafts and vascular patches
  • BS ISO 7198:1998 Cardiovascular implants - Tubular vascular prostheses
  • BS EN ISO 3826-4:2015 Plastics collapsible containers for human blood and blood components. Aphaeresis blood bag systems with integrated features
  • BS EN ISO 25539-1:2017(2018) Cardiovascular implants - Endovascular devices Part 1 : Endovascular prostheses
  • BS EN ISO 10555-2:1997 Sterile, single-use intravascular catheters. Angiographic catheters
  • 19/30385889 DC BS EN ISO 25539-2. Cardiovascular implants. Endovascular devices. Part 2. Vascular stents
  • BS EN ISO 25539-3:2012 Cardiovascular implants. Endovascular devices. Vena cava filters
  • BS EN ISO 10555-2:1997(2003) Sterile, single - use intravascular catheters — Part 2 : Angiographic catheters
  • BS EN ISO 25539-3:2011 Cardiovascular implants. Endovascular devices. Vena cava filters
  • BS ISO 25539-4:2021 Cardiovascular implants. Endovascular devices - Application of ISO 17327-1 for coated endovascular devices
  • BS EN ISO 3826-3:2006 Plastics collapsible containers for human blood and blood components. Blood bag systems with integrated features
  • BS EN ISO 3826-3:2007 Plastics collapsible containers for human blood and blood components - Blood bag systems with integrated features
  • 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
  • 20/30400340 DC BS ISO 25539-4. Cardiovascular implants. Endovascular devices. Part 4. Application of ISO 17327-1 for coated endovascular devices
  • BS DD ISO/TS 12417:2011 Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products
  • BS EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • BS PD ISO/TS 17137:2021 Cardiovascular implants and extracorporeal systems. Cardiovascular absorbable implants
  • 12/30254337 DC BS ISO 8637 AMD1. Cardiovascular implants and extracorporeal systems. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • BS ISO 18242:2016+A1:2023 Cardiovascular implants and extracorporeal systems. Centrifugal blood pumps

SCC

  • BS EN 12006-3:1999 Non-active surgical implants. Particular requirements for cardiac and vascular implants. Endovascular devices
  • BS ISO 25539-1:2003 Cardiovascular implants. Endovascular devices. Endovascular prostheses
  • AAMI/ISO 7198:2016 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches
  • DANSK DS/ISO 25539-2:2020 Cardiovascular implants – Endovascular devices – Part 2: Vascular stents
  • DANSK DS/EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems – Vascular prostheses – Tubular vascular grafts and vascular patches (ISO 7198:2016)
  • DANSK DS/EN 12006-3:1999 Non active surgical implants - Particular requirements for cardiac and vascular implants - Part 3: Endovascular devices
  • AENOR UNE-EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches (ISO 7198:2016)
  • DANSK DS/EN ISO 25539-2:2020 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents
  • AAMI/ISO 25539-2:2008 Cardiovascular implants --Endovascular devices --Part 2: Vascular stents
  • NS-EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems — Vascular prostheses — Tubular vascular grafts and vascular patches (ISO 7198:2016)
  • AAMI/ISO 25539-2:2012 Cardiovascular implants --Endovascular devices --Part 2: Vascular stents
  • NS-EN 12006-3:1998+A1:2009 Non active surgical implants — Particular requirements for cardiac and vascular implants — Part 3: Endovascular devices
  • NS-EN 12006-3:1998 Non active surgical implants — Particular requirements for cardiac and vascular implants — Part 3: Endovascular devices
  • 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
  • AAMI/ISO 25539-1:2017 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses
  • DIN EN 12006-3/A1 E:2009 Draft Document - Non active surgical implants - Particular requirements for cardiac and vascular implants - Part 3: Endovascular devices; English version EN 12006-3:1998/prA1:2008
  • UNE-EN ISO 25539-2:2009 V2 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2008)
  • UNE-EN ISO 25539-2:2009 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2008)
  • NS-EN ISO 25539-2:2009 Cardiovascular implants — Endovascular devices — Part 2: Vascular stents (ISO 25539-2:2008)
  • NS-EN ISO 25539-2:2012 Cardiovascular implants — Endovascular devices — Part 2: Vascular stents (ISO 25539-2:2012)
  • DANSK DS/EN ISO 25539-1:2017 Cardiovascular implants – Endovascular devices – Part 1: Endovascular prostheses (ISO 25539-1:2017)
  • NS-EN ISO 25539-2:2020 Cardiovascular implants — Endovascular devices — Part 2: Vascular stents (ISO 25539-2:2020)
  • NS-EN ISO 25539-2:2008 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2008)
  • NS-EN ISO 25539-1:2017 Cardiovascular implants — Endovascular devices — Part 1: Endovascular prostheses (ISO 25539-1:2017)
  • AS 2636:1983 Sampling of venous and capillary blood for the determination of lead content
  • DIN EN ISO 25539-2 E:2019 Draft Document - Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO/DIS 25539-2:2019); German and English version prEN ISO 25539-2:2019
  • NS-EN 12006-2:1998+A1:2009 Non active surgical implants — Particular requirements for cardiac and vascular implants — Part 2: Vascular prostheses including cardiac valve conduits
  • CAN/CSA Z8637-2008 Cardiovascular Implants and Artificial Organs - Haemodialysers, Haemodiafilters, Haemofilters and Haemoconcentrators (Adopted ISO 8637:2004, second edition, 2004-10-01, with Canadian deviations)
  • UNE-EN ISO 25539-1:2009 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO 25539-1:2003 including Amd 1:2005)
  • NS-EN ISO 25539-1:2009 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO 25539-1:2003 including Amd 1:2005)
  • DIN EN ISO 25539-1 E:2015 Draft Document - Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO/DIS 25539-1:2015); German and English version prEN ISO 25539-1:2015
  • NS-EN ISO 10555-2:1997 Sterile, single-use intravascular catheters - Part 2: Angiographic catheters (ISO 10555-2:1996)
  • DANSK DS/ISO 25539-4:2021 Cardiovascular implants – Endovascular devices – Part 4: Application of ISO 17327-1 for coated endovascular devices
  • NS-EN ISO 25539-1:2008 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO 25539-1:2003 including Amd 1:2005)
  • CAN/CSA Z8638-2008 Cardiovascular Implants and Artificial Organs - Extracorporeal Blood Circuit for Haemodialysers, Haemodiafilters and Haemofilters (Adopted ISO 8638:2004, second edition, 2004-10-01, with Canadian deviations)
  • AS 2636:1988 Sampling of venous and capillary blood for the determination of lead or cadmium concentration
  • DANSK DS/ISO/TS 17137:2019 Cardiovascular implants and extracorporeal systems – Cardiovascular absorbable implants
  • UNE-EN ISO 10555-2:1997 STERILE, SINGLE-USE INTRAVASCULAR CATHETERS. PART 2: ANGIOGRAPHIC CATHETERS. (ISO 10555-2:1996).
  • DANSK DS/EN ISO 25539-3:2012 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters
  • DANSK DS/ISO 18242:2016 Cardiovascular implants and extracorporeal systems – Centrifugal blood pumps
  • AAMI RD16:2007 Cardiovascular implants and artificial organs - Hemodialyzers, hemodiafilters, hemofilters and hemoconcentrators
  • MIL MIL-C-42041-1987 CATHETER, CARDIOVASCULAR (S/S BY A-A-54232)
  • DANSK DS/ISO/TS 12417:2011 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products
  • BS PD ISO/TS 17137:2019 Cardiovascular implants and extracorporeal systems. Cardiovascular absorbable implants
  • AAMI/ISO TIR12417:2011 Cardiovascular implants and extracorporeal systems -- Vascular device-drug combination products
  • DANSK DS/ISO 18242/AMD 1:2016 Cardiovascular implants and extracorporeal systems – Centrifugal blood pumps
  • DANSK DS/EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems – Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators

International Organization for Standardization (ISO)

  • ISO 7198:2016 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches
  • ISO 15674:2001 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
  • ISO 7198:1998 Cardiovascular implants - Tubular vascular prostheses
  • ISO 25539-2:2012 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents
  • ISO 15674:2009 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
  • ISO 25539-1:2017 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses
  • ISO 25539-2:2020 Cardiovascular implants — Endovascular devices — Part 2: Vascular stents
  • ISO 25539-1:2003 Cardiovascular implants — Endovascular devicesPart 1:Endovascular prostheses
  • ISO 25539-2:2008 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents
  • ISO/TS 15539:2000 Cardiovascular implants - Endovascular prostheses
  • ISO 3826-4:2015 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features
  • ISO 7199:1996 Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
  • ISO 25539-1:2003/Amd 1:2005 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses; Amendment 1: Test methods
  • ISO 10555-2:1996 Sterile, single-use intravascular catheters - Part 2: Angiographic catheters
  • ISO 25539-4:2021 Cardiovascular implants — Endovascular devices — Part 4: Application of ISO 17327-1 for coated endovascular devices
  • ISO 2553:2019 Cardiovascular implants — Endovascular devices — Part 4: Application of ISO 17327-1 for coated endovascular devices
  • ISO 5840-2:2021/DAmd 1:2023 Cardiovascular implants
  • ISO/FDIS 25539-3:2024 Cardiovascular implants
  • ISO 5840-1:2021/DAmd 1:2023 Cardiovascular implants
  • ISO 5840-3:2021/DAmd 1:2024 Cardiovascular implants
  • ISO 5840-2:2021/CD Amd 1:2023 Cardiovascular implants
  • ISO 5840-3:2021/CD Amd 1:2023 Cardiovascular implants
  • ISO/DIS 10555-8:2023 Intravascular catheters — Sterile and single-use catheters — Part 8: Catheters for extracorporeal blood treatment
  • ISO 5840-1:2021/CD Amd 1:2023 Cardiovascular implants
  • ISO 13959:2002 Water for haemodialysis and related therapies
  • ISO/CD 25539-3 Cardiovascular implants — Endovascular devices — Part 3: Vena cava filters
  • ISO/TS 17137:2019 Cardiovascular implants and extracorporeal systems — Cardiovascular absorbable implants
  • ISO/DIS 25539-3:2023 Cardiovascular implants — Endovascular devices — Part 3: Vena cava filters
  • ISO/TS 12417:2011 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products
  • ISO 13960:2003 Cardiovascular implants and artificial organs - Plasmafilters
  • ISO 8637:2010 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO 25539-3:2011 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters
  • ISO/TS 17137:2014 Cardiovascular implants and extracorporeal systems - Cardiovascular absorbable implants
  • ISO 8638:2004 Cardiovascular implants and artificial organs - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • ISO 13960:2010 Cardiovascular implants and extracorporeal systems - Plasmafilters
  • ISO/TS 17137:2021 Cardiovascular implants and extracorporeal systems - Cardiovascular absorbable implants

European Committee for Standardization (CEN)

  • EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches
  • EN ISO 25539-2:2009 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents
  • EN ISO 25539-2:2020 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2020)
  • EN ISO 25539-2:2012 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2012)
  • EN ISO 25539-1:2017 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses
  • EN ISO 25539-1:2009 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (Incorporating corrigendum February 2011)
  • EN ISO 25539-2:2008 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents [Superseded: CEN EN 14299]
  • EN ISO 3826-4:2015 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features (ISO 3826-4:2015)
  • EN ISO 25539-3:2011 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO 25539-3:2011)

KR-KS

  • 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 25539-2-2020 Cardiovascular implants — Endovascular devices — Part 2: Vascular stents
  • KS P ISO 25539-1-2017 Cardiovascular implants — Endovascular devices — Part 1: Endovascular prostheses
  • KS P ISO 25539-1-2022 Cardiovascular implants — Endovascular devices — Part 1: Endovascular prostheses
  • KS P ISO 8637-2018 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • KS P ISO 18242-2018 Cardiovascular implants and extracorporeal systems — Centrifugal blood pumps

Korean Agency for Technology and Standards (KATS)

  • KS P ISO 7198:2018 Cardiovascular implants and extracorporeal systems — Vascular prostheses — Tubular vascular grafts and vascular patches
  • KS P ISO 25539-2:2009 Cardiovascular implants-Endovascular devices-Part 2:Vascular stents
  • KS P ISO 25539-1:2010 Cardiovascular implants-Endovascular devices-Part 1:Endovascular prostheses
  • KS P ISO 25539-2:2020 Cardiovascular implants — Endovascular devices — Part 2: Vascular stents
  • KS P ISO 7198:2007 Cardiovascular implants-Tubular vascular prostheses
  • KS P ISO 15539-2007(2012) Cardiovascular implants-Endovascular prostheses
  • KS P ISO 25539-1:2017 Cardiovascular implants — Endovascular devices — Part 1: Endovascular prostheses
  • KS P ISO 7199:2012 Cardiovascular implants and artificial organs-Blood-gas exchangers(oxygenators)
  • KS P 6012-2009 Noninvasive electronic sphygmomanometers
  • KS P ISO 10555-2-2007(2012) Sterile, single-use intravascular catheters-Part 2:Angiographic catheters
  • KS P ISO 10555-2:2007 Sterile, single-use intravascular catheters-Part 2:Angiographic catheters
  • KS P ISO 8637:2018 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • KS P ISO 13959:2009 Water for haemodialysis and related therapies
  • KS P ISO 8638-2012(2017) Cardiovascular implants and extracorporeal systems -Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • KS P ISO 13960:2017 Cardiovascular implants and extracorporeal systems — Plasmafilters
  • 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 13960:2010 Cardiovascular implants and artificial organs-Plasmafilters
  • KS P ISO 8637-2023 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators

American National Standards Institute (ANSI)

GSO

  • BH GSO ISO 7198:2017 Cardiovascular implants -- Tubular vascular prostheses
  • OS GSO ISO 7198:2016 Cardiovascular implants -- Tubular vascular prostheses
  • OS GSO ISO 25539-2:2016 Cardiovascular implants -- Endovascular devices -- Part 2: Vascular stents
  • GSO ISO 25539-2:2016 Cardiovascular implants -- Endovascular devices -- Part 2: Vascular stents
  • GSO ISO 7198:2016 Cardiovascular implants -- Tubular vascular prostheses
  • BH GSO ISO 25539-2:2017 Cardiovascular implants -- Endovascular devices -- Part 2: Vascular stents
  • GSO ISO 25539-1:2016 Cardiovascular implants -- Endovascular devices -- Part 1: Endovascular prostheses
  • BH GSO ISO 25539-1:2017 Cardiovascular implants -- Endovascular devices -- Part 1: Endovascular prostheses
  • OS GSO ISO 25539-1:2016 Cardiovascular implants -- Endovascular devices -- Part 1: Endovascular prostheses
  • GSO ISO 25539-4:2024 Cardiovascular implants — Endovascular devices — Part 4: Application of ISO 17327-1 for coated endovascular devices
  • GSO ISO 13960:2015 Cardiovascular implants and extracorporeal systems -- Plasmafilters
  • 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
  • OS GSO ISO 8637:2016 Cardiovascular implants and extracorporeal systems -- Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • GSO ISO 8637:2016 Cardiovascular implants and extracorporeal systems -- Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • OS GSO ISO/TS 17137:2015 Cardiovascular implants and extracorporeal systems -- Cardiovascular absorbable implants
  • GSO ISO 25539-3:2024 Cardiovascular implants — Endovascular devices — Part 3: Vena cava filters

US-AAMI

  • ANSI/AAMI/ISO 15674:2009 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
  • ANSI/AAMI/ISO 25539-2:2008 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents
  • ANSI/AAMI/ISO 25539-2:2012 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents
  • ANSI/AAMI/ISO 8637:2010 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ANSI/AAMI/ISO TIR12417:2011 Cardiovascular implante and extracorporeal systems - Vascular device-drug combination products
  • ANSI/AAMI RD16-2007 Cardiovascular implants and artificial organs-Hemodialyzers,hemodiafilters,hemofilters,and hemoconcentrators

IT-UNI

German Institute for Standardization

  • 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 25539-2:2021-01 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2020); German version EN ISO 25539-2:2020
  • DIN EN ISO 25539-1:2018-05 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO 25539-1:2017); German version EN ISO 25539-1:2017 / Note: DIN EN ISO 25539-1 (2017-09) and DIN EN ISO 25539-1 (2009-08) remain valid alongside this standard until 202...
  • 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-Fachbericht 153:2006 Von Willebrand Factor Analysis
  • DIN 12750:1969 Blood dilution pipettes for blood corpuscles counting
  • DIN 58987:2024-04 Haemostaseology - Reference method for the Von Willebrand Factor antigen; Text in German and English
  • DIN 58987:2023-04 Haemostaseology - Reference method for the Von Willebrand Factor antigen; Text in German and English / Note: Date of issue 2023-03-03*Intended as replacement for DIN 58987 (2010-03).
  • DIN EN ISO 25539-2:2013 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2012); German version EN ISO 25539-2:2012
  • DIN 58988:2024-04 Haemostaseology - Reference method for the Von Willebrand Factor multimers; Text in German and English
  • DIN EN ISO 25539-2:2009 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2008); German version EN ISO 25539-2:2009
  • DIN EN ISO 25539-1:2018 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO 25539-1:2017); German version EN ISO 25539-1:2017
  • DIN 58988:2023-04 Haemostaseology - Reference method for the Von Willebrand Factor multimers; Text in German and English / Note: Date of issue 2023-03-03*Intended as replacement for DIN 58988 (2010-03).
  • DIN EN ISO 25539-2:2021 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2020); German version EN ISO 25539-2:2020
  • DIN 12845:1972 Westergren tubes for the erythrocyte sedimentation rate of red blood corpuscles
  • DIN EN ISO 25539-1:2017 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO 25539-1:2017); German version EN ISO 25539-1:2017
  • DIN EN ISO 25539-3:2012-03 Cardiovascular implants - Endovascular devices - Part 3: Vena cava filters (ISO 25539-3:2011); German version EN ISO 25539-3:2011
  • DIN 58910-4:2000-03 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 4: Reference measurement procedure for the determination in capillary blood

RU-GOST R

AENOR

  • UNE-EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches (ISO 7198:2016)
  • UNE-EN ISO 25539-2:2013 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2012)
  • UNE-EN ISO 25539-1:2009 V2 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO 25539-1:2003 including Amd 1:2005)

ES-UNE

  • UNE-EN ISO 25539-2:2021 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2020)
  • UNE-EN ISO 25539-1:2017 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO 25539-1:2017) (Endorsed by Asociación Española de Normalización in June of 2017.)

Danish Standards Foundation

Standard Association of Australia (SAA)

  • AS ISO 15539:2003(R2014) Cardiovascular Implants Endovascular Prostheses
  • AS 2636:1994 Sampling of venous and capillary blood for the determination of lead or cadmium concentration

Military Standards (MIL-STD)

CH-SNV

  • SN EN ISO 25539-2:2021 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2020)

Lithuanian Standards Office

  • LST EN ISO 25539-2:2020 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2020)
  • LST EN ISO 25539-2:2013 Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539-2:2012)
  • LST EN ISO 25539-1:2009/AC:2011 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO 25539-1:2003 including Amd 1:2005)
  • LST EN ISO 25539-1:2009 Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO 25539-1:2003 including Amd 1:2005)
  • LST EN ISO 10555-2:2001 Sterile, single-use intravascular catheters - Part 2: Angiographic catheters (ISO 10555-2:1996)
  • LST EN ISO 10555-2:2001/AC:2002 Sterile, single-use intravascular catheters - Part 2: Angiographic catheters (ISO 10555-2:1996/Cor.1:2002)

AT-ON

PL-PKN

GOSTR

  • GOST R 59153-2020 Cardiovascular implants. Endovascular devices. Vascular stents. Technical requirements for governmental purchases

DIN

  • DIN EN 12006-2:1998 Non-active surgical implants - Particular requirements for cardiac and vascular implants - Part 2: Vascular prostheses including cardiac valve conduits; German version EN 12006-2:1998
  • DIN EN 12006-3:2009 Non active surgical implants - Particular requirements for cardiac and vascular implants - Part 3: Endovascular devices (includes Amendment A1:2009)
  • DIN 58987:2024 Haemostaseology - Reference method for the Von Willebrand Factor antigen; Text in German and English
  • DIN 58988:2024 Haemostaseology - Reference method for the Von Willebrand Factor multimers; Text in German and English
  • DIN EN 1060-2:1996 Non-invasive sphygmomanometers - Supplementary requirements for mechanical sphygmomanometers

IN-BIS

  • IS 10916-1984 Specification for vacuum tubes for collecting blood specimens (vacuum blood collection tubes)
  • IS 10577-1982 Blood collection tube specifications
  • IS 7971-1975 Tourniquet Specifications Cardiovascular RUMEL-BELMONT Pattern
  • IS 9430-1980 Tube and blood meter specifications
  • IS 8317-1991 Cardiovascular Surgical Instruments - Clamp Vessel Angle 45° - Shape and Dimensions

American Society for Testing and Materials (ASTM)

VN-TCVN

  • TCVN 7609-2-2007 Sterile, single-use intravascular catheters.Part 2: Angiographic catheters

US-FCR

GOST

CZ-CSN

Indonesia Standards

  • SNI ISO 13959:2010 Water for haemodialysis and related therapies
  • SNI 16-6355.5-2000 Steril, single-use intravascular catheters - Intravena catheters
  • SNI ISO 8638:2012 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters

Canadian Standards Association (CSA)

  • CSA Z8637-08-CAN/CSA-2008 Cardiovascular implants and artificial organs ?Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators