Taiwan FDA registration 9e0f1a0975e6a1a32062a2db099508c3
“SYNTEC” Cannulated Screw System
TW: “亞太醫療”中空骨釘系統
Taiwan·Risk Class 2·MD·SYNTEC SCIENTIFIC CORPORATION·Registered Dec 31, 2021 – Dec 31, 2026ActiveRegistration details
- Analysis ID
- 9e0f1a0975e6a1a32062a2db099508c3
- License Form
- Ministry of Health Medical Device Manufacturing No. 007355
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)
- N3040 Smooth or threaded metal bone fixation
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 31, 2021
- Expiry Date
- Dec 31, 2026
About this record
Access comprehensive regulatory information for “SYNTEC” Cannulated Screw System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9e0f1a0975e6a1a32062a2db099508c3 and manufactured by SYNTEC SCIENTIFIC CORPORATION. The authorized representative in Taiwan is SYNTEC SCIENTIFIC CORPORATION.
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