Taiwan FDA registration 192b4d333a2f61b95b27a0230db3ff34
“BIOTEQ” Drainage Catheter (Long-term Type)
TW: “邦特”引流導管(長效型)
Taiwan·Risk Class 2·MD·Bonte Biotechnology Co., Ltd. Yilan Plant 2·Registered Mar 19, 2019 – Mar 19, 2029ActiveRegistration details
- Analysis ID
- 192b4d333a2f61b95b27a0230db3ff34
- License Form
- Ministry of Health Medical Device Manufacturing No. 006325
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)
- H5010 Bile ductal catheters and their accessories
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 19, 2019
- Expiry Date
- Mar 19, 2029
About this record
Access comprehensive regulatory information for “BIOTEQ” Drainage Catheter (Long-term Type) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 192b4d333a2f61b95b27a0230db3ff34 and manufactured by Bonte Biotechnology Co., Ltd. Yilan Plant 2. The authorized representative in Taiwan is BIOTEQUE CORPORATION.
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