Taiwan FDA registration 781fbdde7e7b47ce0ee57d03c2e3c27c
"Kejie" narrow body artificial tooth root
TW: “可捷”窄體人工牙根
Taiwan·Risk Class 3·KJ MEDITECH CO., LTD.·Registered Nov 21, 2011 – Nov 21, 2026ActiveRegistration details
- Analysis ID
- 781fbdde7e7b47ce0ee57d03c2e3c27c
- Customs Code
- DHA00602301704
Company information
- Manufacturer
- KJ MEDITECH CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- FUGINGTONE CO.
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
- Nov 21, 2011
- Expiry Date
- Nov 21, 2026
About this record
Access comprehensive regulatory information for "Kejie" narrow body artificial tooth root in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 781fbdde7e7b47ce0ee57d03c2e3c27c and manufactured by KJ MEDITECH CO., LTD.. The authorized representative in Taiwan is FUGINGTONE CO..
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