Taiwan FDA registration ed0f6b55e7564fc4d31505daef4bc8c8
"Sandops" Teshd regeneration membrane
TW: “山多普斯”泰仕德再生膜
Taiwan·Risk Class 2·OSTEOGENICS BIOMEDICAL, INC.·Registered Jul 08, 2013 – Jul 08, 2028ActiveRegistration details
- Analysis ID
- ed0f6b55e7564fc4d31505daef4bc8c8
- Customs Code
- DHA00602517101
Company information
- Manufacturer
- OSTEOGENICS BIOMEDICAL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- OSSTEM CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3930 Alveolar repair materials
- Import Information
- import
Dates and status
- Registration Date
- Jul 08, 2013
- Expiry Date
- Jul 08, 2028
About this record
Access comprehensive regulatory information for "Sandops" Teshd regeneration membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed0f6b55e7564fc4d31505daef4bc8c8 and manufactured by OSTEOGENICS BIOMEDICAL, INC.. The authorized representative in Taiwan is OSSTEM CORPORATION.
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