Taiwan FDA registration 58843812418be5fcbe5be1762f992a4c
“SYNTEC” Steinmann wire
TW: “亞太醫療”史氏骨針
Taiwan·Risk Class 2·MD·SYNTEC SCIENTIFIC CORPORATION·Registered Jul 27, 2022 – Jul 27, 2027ActiveRegistration details
- Analysis ID
- 58843812418be5fcbe5be1762f992a4c
- License Form
- Ministry of Health Medical Device Manufacturing No. 007517
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
- Jul 27, 2022
- Expiry Date
- Jul 27, 2027
About this record
Access comprehensive regulatory information for “SYNTEC” Steinmann wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 58843812418be5fcbe5be1762f992a4c and manufactured by SYNTEC SCIENTIFIC CORPORATION. The authorized representative in Taiwan is SYNTEC SCIENTIFIC CORPORATION.
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