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Stent for the treatment of branch artery dilation - Vietnam Registration 2402740ĐKLH/BYT-HTTB

Access comprehensive regulatory information for Stent for the treatment of branch artery dilation 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 2402740ĐKLH/BYT-HTTB and manufactured by phenox GmbH. The authorized representative in Vietnam is CÔNG TY TNHH ANDAMAN MEDICAL VIỆT NAM.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Theo theo phụ lục, and 1 recent registrations in the same category. Pure Global AI offers free access to 300,000+ Vietnamese medical device registrations, helping global MedTech companies navigate Vietnam MOH regulations, identify competitors, and discover partnership opportunities efficiently.

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2402740ĐKLH/BYT-HTTB
Registration Details
Vietnam MOH Registration: 2402740ĐKLH/BYT-HTTB
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Device Details

Stent for the treatment of branch artery dilation
VN: Stent phình động mạch phân nhánh
Risk Class TTBYT Loại D

Registration Details

2402740ĐKLH/BYT-HTTB

19008669/ĐKLH-BYT-TB-CT

Theo theo phụ lục

Theo phụ lục

Company Information

Theo theo phụ lục

phenox GmbH

Technical Details

Stent phình động mạch phân nhánh is used to treat the in-stent restenosis of the common carotid artery in the internal carotid arteries.

Dates and Status

Oct 02, 2024

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