Taiwan FDA registration c6451cd8267913b80efdb0250d1c287e
“Cytoplast” TXT Regenerative Barrier Membrane
TW: “山多普斯”特仕德再生膜
Taiwan·Risk Class 2·MD·OSTEOGENICS BIOMEDICAL, INC.·Registered Jul 25, 2013 – Jul 25, 2028ActiveRegistration details
- Analysis ID
- c6451cd8267913b80efdb0250d1c287e
- License Form
- Ministry of Health Medical Device Import No. 025194
- Customs Code
- DHA05602519403
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 Dental devices
- Product Type (Level 2)
- F3930 Tricalcium phosphate for alveolar bone restoration
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 25, 2013
- Expiry Date
- Jul 25, 2028
About this record
Access comprehensive regulatory information for “Cytoplast” TXT Regenerative Barrier Membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c6451cd8267913b80efdb0250d1c287e and manufactured by OSTEOGENICS BIOMEDICAL, INC.. The authorized representative in Taiwan is OSSTEM CORPORATION.
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