Taiwan FDA registration 1fc131eefbf6c26d322ee420702a1a81
"Marani" Bomeng multi-porous biphasic artificial replacement bone gel
TW: “瑪蘭尼”博萌得多孔雙相人工替代骨凝膠
Taiwan·Risk Class 3·BIOMATLANTE·Registered Mar 05, 2009 – Mar 05, 2019CancelledRegistration details
- Analysis ID
- 1fc131eefbf6c26d322ee420702a1a81
- Customs Code
- DHA00601968708
Company information
- Manufacturer
- BIOMATLANTE
- Manufacturer Country
- France
- Authorized Representative
- ALSTRONG SCIENTIFIC INTERNATIONAL LTD.
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
- Mar 05, 2009
- Expiry Date
- Mar 05, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Marani" Bomeng multi-porous biphasic artificial replacement bone gel in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1fc131eefbf6c26d322ee420702a1a81 and manufactured by BIOMATLANTE. The authorized representative in Taiwan is ALSTRONG SCIENTIFIC INTERNATIONAL LTD..
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