Taiwan FDA registration 49b4daa92aa4995570a13d06d7fe3ae2
"Daleden" root tube expansion (unsterilized)
TW: “戴爾登”根管擴大材 (未滅菌)
Taiwan·Risk Class 1·DIADENT GROUP INTERNATIONAL·Registered Jan 17, 2007 – Jan 17, 2027ActiveRegistration details
- Analysis ID
- 49b4daa92aa4995570a13d06d7fe3ae2
- Customs Code
- DHA04400553900
Company information
- Manufacturer
- DIADENT GROUP INTERNATIONAL
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- TUNG SHENG INTERNATIONAL INC.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of dental hand instruments (F.4565).
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4565 牙科手用器械
- Import Information
- import
Dates and status
- Registration Date
- Jan 17, 2007
- Expiry Date
- Jan 17, 2027
About this record
Access comprehensive regulatory information for "Daleden" root tube expansion (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 49b4daa92aa4995570a13d06d7fe3ae2 and manufactured by DIADENT GROUP INTERNATIONAL. The authorized representative in Taiwan is TUNG SHENG INTERNATIONAL INC..
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