Taiwan FDA registration a121e02481e5ea4bd5b0cd5acf56fb5e
“Dio” UF implant system-Angled abutment
TW: “帝歐”悠福植體系統-角度式支台齒
Taiwan·Risk Class 2·MD·DIO CORPORATION·Registered Jul 27, 2017 – Jul 27, 2027ActiveRegistration details
- Analysis ID
- a121e02481e5ea4bd5b0cd5acf56fb5e
- License Form
- Ministry of Health Medical Device Import No. 030031
- Customs Code
- DHA05603003108
Company information
- Manufacturer
- DIO CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- DIO IMPLANT TAIWAN CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3630 Dental bridges for bone explants
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 27, 2017
- Expiry Date
- Jul 27, 2027
About this record
Access comprehensive regulatory information for “Dio” UF implant system-Angled abutment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a121e02481e5ea4bd5b0cd5acf56fb5e and manufactured by DIO CORPORATION. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.
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