Taiwan FDA registration 26b832e2841190aa7fc4fa9b50f53606
Components of the "Ashuffis" artificial tooth root implant system
TW: “艾秀菲絲”人工牙根植體系統零組件
Taiwan·Risk Class 2·OSSEOFUSE INC.;; KJ MEDITECH CO., LTD.·Registered Jan 24, 2022 – Dec 07, 2026ActiveRegistration details
- Analysis ID
- 26b832e2841190aa7fc4fa9b50f53606
- Customs Code
- DHA05602920400
Company information
- Manufacturer
- OSSEOFUSE INC.;; KJ MEDITECH CO., LTD.
- Manufacturer Country
- Korea, Republic of;;United States
- Authorized Representative
- LEGREEN PROPERTIES LIMITED, TAIWAN BRANCH BVI
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.3630 Bolsters for intraosseous implants
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Jan 24, 2022
- Expiry Date
- Dec 07, 2026
About this record
Access comprehensive regulatory information for Components of the "Ashuffis" artificial tooth root implant system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 26b832e2841190aa7fc4fa9b50f53606 and manufactured by OSSEOFUSE INC.;; KJ MEDITECH CO., LTD.. The authorized representative in Taiwan is LEGREEN PROPERTIES LIMITED, TAIWAN BRANCH BVI.
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