Taiwan FDA registration f518cb38e845c783f44aeaf028520777
“BIOMATLANTE” MBCP+ Bone Graft Substitute
TW: “博美蘭”莫希比加多孔人工替代骨
Taiwan·Risk Class 2·MD·BIOMATLANTE·Registered Sep 30, 2015 – Sep 30, 2020CancelledRegistration details
- Analysis ID
- f518cb38e845c783f44aeaf028520777
- License Form
- Ministry of Health Medical Device Import No. 027805
- Customs Code
- DHA05602780503
Company information
- Manufacturer
- BIOMATLANTE
- Manufacturer Country
- France
- Authorized Representative
- Polytechnic Technology Engineering Consultants Limited
Product details
- 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
- Sep 30, 2015
- Expiry Date
- Sep 30, 2020
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for “BIOMATLANTE” MBCP+ Bone Graft Substitute in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f518cb38e845c783f44aeaf028520777 and manufactured by BIOMATLANTE. The authorized representative in Taiwan is Polytechnic Technology Engineering Consultants Limited.
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