Taiwan FDA registration d2721577d43065487980731e51f1da5c
“BIOTEQ”Micro Catheter Kit
TW: “邦特”微導管套組
Taiwan·Risk Class 2·MD·Bonte Biotechnology Co., Ltd. Yilan Plant 2·Registered Jul 25, 2022 – Jul 25, 2027ActiveRegistration details
- Analysis ID
- d2721577d43065487980731e51f1da5c
- License Form
- Ministry of Health Medical Device Manufacturing No. 007661
Company information
- Manufacturer
- Bonte Biotechnology Co., Ltd. Yilan Plant 2
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOTEQUE CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 25, 2022
- Expiry Date
- Jul 25, 2027
About this record
Access comprehensive regulatory information for “BIOTEQ”Micro Catheter Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d2721577d43065487980731e51f1da5c and manufactured by Bonte Biotechnology Co., Ltd. Yilan Plant 2. The authorized representative in Taiwan is BIOTEQUE CORPORATION.
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