Taiwan FDA registration cef7f22bd3aa977a3e009a834a504e30
“Diadent” EDTA Root Canal Preparator (Non-Sterile)
TW: “戴爾特” 根管擴大材 (未滅菌)
Taiwan·Risk Class 1·MD·DIADENT GROUP INTERNATIONAL·Registered Dec 10, 2018 – Dec 10, 2023ExpiredRegistration details
- Analysis ID
- cef7f22bd3aa977a3e009a834a504e30
- License Form
- Ministry of Health Medical Device Import No. 019901
- Customs Code
- DHA09401990100
Company information
- Manufacturer
- DIADENT GROUP INTERNATIONAL
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- HONG SHIN DENTAL MATERIAL CO., LTD
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 10, 2018
- Expiry Date
- Dec 10, 2023
About this record
Access comprehensive regulatory information for “Diadent” EDTA Root Canal Preparator (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cef7f22bd3aa977a3e009a834a504e30 and manufactured by DIADENT GROUP INTERNATIONAL. The authorized representative in Taiwan is HONG SHIN DENTAL MATERIAL CO., LTD.
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