Taiwan FDA registration df42dbbfbd5aae696a17427d8e881920
“BONTEQ” Angiographic Catheters
TW: “全保”血管攝影導管
Taiwan·Risk Class 2·MD·Bonte Biotechnology Co., Ltd. Yilan Plant 2·Registered Sep 05, 2018 – Sep 04, 2026ActiveRegistration details
- Analysis ID
- df42dbbfbd5aae696a17427d8e881920
- License Form
- Ministry of Health Medical Device Manufacturing No. 006150
Company information
- Manufacturer
- Bonte Biotechnology Co., Ltd. Yilan Plant 2
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOTEQUE CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1200 Diagnostic endovascular catheter
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 05, 2018
- Expiry Date
- Sep 04, 2026
About this record
Access comprehensive regulatory information for “BONTEQ” Angiographic Catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df42dbbfbd5aae696a17427d8e881920 and manufactured by Bonte Biotechnology Co., Ltd. Yilan Plant 2. The authorized representative in Taiwan is BIOTEQUE CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices