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Database: 365,228(8 Aug 2026)

In vitro blood vessels

In vitro blood vessels, Total:66 items.

The international standard classification for "In vitro blood vessels" includes: Surgical instruments and materials .

The Chinese standard classification for "In vitro blood vessels" includes: Medical apparatus and devices in general .


未注明发布机构

  • ANSI/AAMI/ISO 12417-1:2015 Cardiovascular implants and extracorporeal systems— Vascular device-drug combination products— Part 1: General requirements
  • DIN EN ISO 12417-1 E:2021-11 Cardiovascular grafts and extracorporeal system vascular devices for combined use of drugs - Part 1: General requirements (draft)
  • ANSI/AAMI/ISO 7198:2016 Cardiovascular implants and extracorporeal systems— Vascular prostheses—Tubular vascular grafts and vascular patches
  • DIN EN ISO 12417-1 E:2014-06 Cardiovascular grafts and extracorporeal system vascular devices for combined use of drugs - Part 1: General requirements (draft)
  • DIN EN ISO 7198 E:2014-10 Cardiovascular Implants and Extracorporeal Systems Vascular Prostheses Tubular Vascular Grafts and Vascular Patches (Draft)

国家药监局

  • YY/T 1764-2021 Standard guide for in vitro axial,bending,and torsional durability testing of vascular stents

Professional Standard - Medicine

  • YY/T 0808-2010 Standard test methods for in vitro pulsatile durability testing of vascular stents

Group Standards of the People's Republic of China

  • T/CSBM 0050.4-2024 Effectiveness evaluation of wound repair materials Part 3:In vitro microangiogenesis evaluation method

International Organization for Standardization (ISO)

  • ISO 7198:2016 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches
  • ISO/TS 12417:2011 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products
  • 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 12417-1:2015 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements
  • ISO 12417-1:2023 Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 1: General requirements
  • ISO/PRF 12417-1:2011 Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 1: General requirements
  • ISO/DIS 12417-1 Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 1: General requirements
  • ISO/TR 12417-2:2022 Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 2: Local regulatory information
  • ISO/TR 12417-2:2017 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 2: Local regulatory information

Association Francaise de Normalisation

  • 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 S94-710-1*NF EN ISO 12417-1:2015 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1 : general requirements

British Standards Institution (BSI)

  • BS EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems. Vascular prostheses. Tubular vascular grafts and vascular patches
  • BS DD ISO/TS 12417:2011 Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products
  • 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 EN ISO 12417-1:2015 Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products. General requirements
  • BS EN ISO 12417-1:2024 Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products - General requirements
  • BS PD ISO/TS 17137:2021 Cardiovascular implants and extracorporeal systems. Cardiovascular absorbable implants
  • PD ISO/TR 12417-2:2022 Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products. Local regulatory information

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

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

SCC

  • AAMI/ISO 7198:2016 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches
  • 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 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)
  • AAMI/ISO TIR12417:2011 Cardiovascular implants and extracorporeal systems -- Vascular device-drug combination products
  • DANSK DS/ISO/TS 12417:2011 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products
  • 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/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
  • BS PD ISO/TR 12417-2:2022 Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products-Local regulatory information
  • DIN EN ISO 12417-1 E:2014 Draft Document - Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products (ISO/DIS 12417-1:2014); German version prEN ISO 12417-1:2014
  • DANSK DS/EN ISO 12417-1:2015 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements
  • DANSK DS/ISO/TR 12417-2:2022 Cardiovascular implants and extracorporeal systems – Vascular device-drug combination products – Part 2: Local regulatory information
  • AAMI/ISO 12417-1:2015 Cardiovascular implants and extracorporeal systems - Vascular device-drugcombination products - Part 1: General requirements
  • AENOR UNE-EN ISO 12417-1:2016 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2015)
  • NS-EN ISO 12417-1:2024 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2024)

European Committee for Standardization (CEN)

  • EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches
  • EN ISO 12417-1:2015 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2015)
  • EN ISO 12417-1:2024 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2024)
  • prEN ISO 12417-1:2021 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO/DIS 12417-1:2021)

AENOR

  • UNE-EN ISO 7198:2017 Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches (ISO 7198:2016)

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 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 EN ISO 12417-1:2016-02 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2015); German version EN ISO 12417-1:2015 / Note: To be replaced by DIN EN ISO 12417-1 (2021-11).

US-AAMI

Danish Standards Foundation

  • DS/ISO/TS 12417:2011 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products
  • DS/ISO/TS 17137:2021 Cardiovascular implants and extracorporeal systems – Cardiovascular absorbable implants

American Society for Testing and Materials (ASTM)

  • ASTM F2477-23 Standard Test Methods for in vitro Pulsatile Durability Testing of Vascular Stents and Endovascular Prostheses

GSO

  • OS GSO ISO/TS 17137:2015 Cardiovascular implants and extracorporeal systems -- Cardiovascular absorbable implants
  • GSO ISO 12417-1:2021 Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 1: General requirements
  • BH GSO ISO 12417-1:2022 Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 1: General requirements

GOSTR

  • GOST R ISO 12417-1-2019 Cardiovascular implants and extracorporeal systems. Vascular device-drug combination products. Part 1. General requirements

ES-UNE

  • UNE-EN ISO 12417-1:2016 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products - Part 1: General requirements (ISO 12417-1:2015)