160206
IV
Delisted
Stent/Grafts, Vascular, Aorticๆฏๆถ/็งปๆค็ฉ๏ผ่ก็ฎก๏ผไธปๅจ่
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
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Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
IV
Product Code
20453
State
N/A
Status
Delisted
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Manufacturer (่ฃฝ้ ๅ)
JOTEC GmbH
Artivion (Formerly Cryolife)
Germany
ๅพทๅฝ
Lotzenaecker 23, 72379 Hechingen, Germany
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Authorised Representative (AR)
27863233
Regulatory Timeline
Registration Date
June 21, 2016
Expiry Date
June 21, 2021
Delist Date
December 22, 2020
Remarks
Delisted.
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Product Models
E-vita Open plus Stent Graft System