

ISO/TR 12417-2-2017 心血管移植和體外系統--血管設備藥物組合產(chǎn)品--第2部分:地方法規信息 Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 2: Local regulatory information
- 標準類(lèi)別:
- 標準大?。?/li>
- 標準編號:ISO/TR 12417-2-2017
- 標準狀態(tài):現行
- 更新時(shí)間:2023-11-17
- 下載次數:次
This document provides region-specific information for
— local submissions and approvals for vascular device-drug combination products (VDDCPs) in countries and regions around the world;
— changes related to the drug containing part and how they are evaluated by the different local regions.
For implanted products, this document is considered as a supplement to ISO 14630, which specifies general requirements for the performance of non-active surgical implants.
This document is considered also as a supplement to ISO 12417-1, and any relevant device-specific standards, such as the ISO 25539 series specifying requirements for endovascular devices. Requirements listed in this document also address VDDCPs that are not necessarily permanent implants.st edition
2017-11
Cardiovascular implants and
extracorporeal systems — Vascular
device-drug combination products —
Part 2:
Local regulatory information
Implants cardiovasculaires et circuits extra-corporels — Produits de
combinaison médicament-dispositif vasculaire —
Partie 2: Directives règlementaires locales
Reference number
ISO/TR 12417-2:2017(E)
?
ISO 2017
ISO/TR 12417-2:2017(E)
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