Penumbra for Neurovascular Intervention - Vietnam Registration 2400917ĐKLH/BYT-HTTB
Access comprehensive regulatory information for Penumbra for Neurovascular Intervention in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại D medical device is registered under number 2400917ĐKLH/BYT-HTTB and manufactured by phenox GmbH. The authorized representative in Vietnam is CÔNG TY TNHH VẬT TƯ PTCA ALCO VIỆT NAM.
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Device Details
Registration Details
2400917ĐKLH/BYT-HTTB
000.00.04.G18-231012-0008
Theo theo phụ lục
Theo phụ lục
Technical Details
Used to extend the stent scaffold and the flow diversion scaffold in cases where the stent scaffold is not yet in close apposition to the blood vessel wall in the intracranial and extracranial vessels supplying the brain in patients with restenosis after angioplasty and/or placement of a stent or flow diversion.
Dates and Status
Jul 21, 2024