Vietnam MOH registration 240000794/PCBB-HCM

Angioplasty guidewire, femoral artery pathway.

VN: Bộ dụng cụ mở đường mạch máu đường quay, đường đùi.
Vietnam flagVietnam·Risk Class TTBYT Loại B·Theo theo phụ lục·Bioteque Corporation·Registered Apr 12, 2024
Registration details
Analysis ID
240000794/PCBB-HCM
Submission ID
000.00.19.H29-240324-0004
Product Type
Theo theo phụ lục
Product Code
Theo phụ lục
Company information
Manufacturer Country
Theo theo phụ lục
Product Owner
Bioteque Corporation
Technical details
Intended Use
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
Registration Date
Apr 12, 2024
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About this record

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.

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