160206

Stent/Grafts, Vascular, Aortic

支架/移植物,血管,主动脉
JOTEC GmbH·IV·Hong Kong MDACS·Registered June 21, 2016Delisted
Device overview
Risk class
IV
Product code
20453
State
N/A
Status
Delisted
已退市
Manufacturer (製造商)
Name
JOTEC GmbH
Artivion (Formerly Cryolife)
Country
Germany
德国
Address
Lotzenaecker 23, 72379 Hechingen, Germany
德国海琴根,Lotzenaecker 23,72379
Authorised representative (AR)
Phone
27863233
Regulatory timeline
Registration date
June 21, 2016
Expiry date
June 21, 2021
Delist date
December 22, 2020
Product models
E-vita Open plus Stent Graft System
Remarks
Delisted.
已從列表中刪除。
About this record

This profile provides complete Hong Kong MDACS registration information for Stent/Grafts, Vascular, Aortic. Review device classification, authorised representative (AR) details, manufacturer contacts, product codes, and regulatory milestones. Pure Global AI delivers bilingual transparency for medical device registrations across Asia.

Product Info: Stent/Grafts, Vascular, Aortic

產品資訊: 支架/移植物,血管,主动脉