Taiwan FDA registration 555eb3d636a5d8e79043130d70414f90
“Dio” UF(II) Multi abutment
TW: “帝歐”悠福複合型基台
Taiwan·Risk Class 2·MD·DIO CORPORATION·Registered Mar 22, 2018 – Mar 22, 2028ActiveRegistration details
- Analysis ID
- 555eb3d636a5d8e79043130d70414f90
- License Form
- Ministry of Health Medical Device Import No. 030988
- Customs Code
- DHA05603098808
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
- Mar 22, 2018
- Expiry Date
- Mar 22, 2028
About this record
Access comprehensive regulatory information for “Dio” UF(II) Multi abutment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 555eb3d636a5d8e79043130d70414f90 and manufactured by DIO CORPORATION. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.
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