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
- ANSI/AAMI/ISO TIR12417:2011 Cardiovascular implante and extracorporeal systems - Vascular device-drug combination products
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)
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