Angioplasty guidewire, femoral artery pathway. - Vietnam Registration 240000794/PCBB-HCM
Access comprehensive regulatory information for Angioplasty guidewire, femoral artery pathway. in Vietnam's medical device market through Pure Global AI's free database. This Risk Class TTBYT Loại B medical device is registered under number 240000794/PCBB-HCM and manufactured by Bioteque Corporation. The authorized representative in Vietnam is CÔNG TY TNHH TRANG THIẾT BỊ VÀ VẬT TƯ Y TẾ HOÀNG VIỆT LONG.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Bioteque Corporation, 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.
Device Details
Registration Details
240000794/PCBB-HCM
000.00.19.H29-240324-0004
Theo theo phụ lục
Theo phụ lục
Technical Details
Angioplasty is a procedure aimed at creating a pathway in the blood vessels to facilitate the passage of various instruments through the skin into the peripheral veins or arteries
Dates and Status
Apr 12, 2024