Taiwan FDA registration d405039d2756a1c6562300d66a9d83c6
“BONTEQ” Ureteral Stent Set
TW: “全保”輸尿管導管組
Taiwan·Risk Class 2·MD·Bonte Biotechnology Co., Ltd. Yilan Plant 2·Registered Jul 30, 2018 – Jun 10, 2027ActiveRegistration details
- Analysis ID
- d405039d2756a1c6562300d66a9d83c6
- License Form
- Ministry of Health Medical Device Manufacturing No. 006167
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)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H4620 Ureteral stents
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 30, 2018
- Expiry Date
- Jun 10, 2027
About this record
Access comprehensive regulatory information for “BONTEQ” Ureteral Stent Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d405039d2756a1c6562300d66a9d83c6 and manufactured by Bonte Biotechnology Co., Ltd. Yilan Plant 2. The authorized representative in Taiwan is BIOTEQUE CORPORATION.
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