Taiwan FDA registration 31a5b2b7be809460f4a816d3e60905d8
"Anshufi" inner octagonal tooth root implant and its appendages
TW: “安舒菲”內八角牙根型植體及其附件
Taiwan·Risk Class 3·ANTHOGYR SAS·Registered Jun 14, 2007 – Jun 14, 2022CancelledRegistration details
- Analysis ID
- 31a5b2b7be809460f4a816d3e60905d8
- Customs Code
- DHA00601812207
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
- Jun 14, 2007
- Expiry Date
- Jun 14, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Anshufi" inner octagonal tooth root implant and its appendages in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 31a5b2b7be809460f4a816d3e60905d8 and manufactured by ANTHOGYR SAS. The authorized representative in Taiwan is TSENG LIMITED.
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