Taiwan FDA registration b7b579bfd6eb72f2e62fef8b22305074
"Asia-Pacific Medical" fine mesh titanium bone plate system
TW: “亞太醫療”精微網狀鈦骨板系統
Taiwan·Risk Class 2·SYNTEC SCIENTIFIC CORPORATION·Registered Oct 05, 2011 – Oct 05, 2026ActiveRegistration details
- Analysis ID
- b7b579bfd6eb72f2e62fef8b22305074
- Customs Code
- DHY00500346502
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)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3300 Surgical mesh
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 05, 2011
- Expiry Date
- Oct 05, 2026
About this record
Access comprehensive regulatory information for "Asia-Pacific Medical" fine mesh titanium bone plate system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b7b579bfd6eb72f2e62fef8b22305074 and manufactured by SYNTEC SCIENTIFIC CORPORATION. The authorized representative in Taiwan is SYNTEC SCIENTIFIC CORPORATION.
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