Taiwan FDA registration 48addd0c6e08c1e56ac2be579cfa3780
“SYNTEC” D Fit-Titanium Vertebral Interbody Cage
TW: “亞太醫療”雙合-鈦合金椎間融合器
Taiwan·Risk Class 2·MD·SYNTEC SCIENTIFIC CORPORATION·Registered May 06, 2020 – May 06, 2025ExpiredRegistration details
- Analysis ID
- 48addd0c6e08c1e56ac2be579cfa3780
- License Form
- Ministry of Health Medical Device Manufacturing No. 006693
Company information
- Manufacturer
- SYNTEC SCIENTIFIC CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SYNTEC SCIENTIFIC CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3080 Interbody fusion device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 06, 2020
- Expiry Date
- May 06, 2025
About this record
Access comprehensive regulatory information for “SYNTEC” D Fit-Titanium Vertebral Interbody Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 48addd0c6e08c1e56ac2be579cfa3780 and manufactured by SYNTEC SCIENTIFIC CORPORATION. The authorized representative in Taiwan is SYNTEC SCIENTIFIC CORPORATION.
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