Taiwan FDA registration e98e5be004627b3fc0a9b8603bc44c12
Oshifi implant system
TW: 歐仕菲植體系統
Taiwan·Risk Class 3·ANTHOGYR SAS·Registered Apr 20, 2009 – Apr 20, 2019CancelledRegistration details
- Analysis ID
- e98e5be004627b3fc0a9b8603bc44c12
- Customs Code
- DHA00601978903
Company information
- Manufacturer
- ANTHOGYR SAS
- Manufacturer Country
- France
- Authorized Representative
- TSENG LIMITED
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.3640 Bone Implants
- Import Information
- import
Dates and status
- Registration Date
- Apr 20, 2009
- Expiry Date
- Apr 20, 2019
- Cancellation Date
- Nov 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Oshifi implant system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e98e5be004627b3fc0a9b8603bc44c12 and manufactured by ANTHOGYR SAS. The authorized representative in Taiwan is TSENG LIMITED.
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