Taiwan FDA registration bc139d02629e31d011f3baaaa49aad4c
“SYNTEC” CB-Cervical Cage System
TW: “亞太醫療”亞可-頸椎護架系統
Taiwan·Risk Class 2·MD·SYNTEC SCIENTIFIC CORPORATION·Registered Jun 07, 2023 – Jun 07, 2028ActiveRegistration details
- Analysis ID
- bc139d02629e31d011f3baaaa49aad4c
- License Form
- Ministry of Health Medical Device Manufacturing No. 007871
Company information
- Manufacturer
- SYNTEC SCIENTIFIC CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SYNTEC SCIENTIFIC CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N3080 Interbody fusion device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jun 07, 2023
- Expiry Date
- Jun 07, 2028
About this record
Access comprehensive regulatory information for “SYNTEC” CB-Cervical Cage System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bc139d02629e31d011f3baaaa49aad4c and manufactured by SYNTEC SCIENTIFIC CORPORATION. The authorized representative in Taiwan is SYNTEC SCIENTIFIC CORPORATION.
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