Taiwan FDA registration 4b2f28f196302a44f324501e277d0cb7
"Diou" dental intraosseous implant attachment (unsterilized)
TW: "帝歐" 牙齒骨內植入物附件 (未滅菌)
Taiwan·Risk Class 1·DIO CORPORATION·Registered Dec 13, 2019 – Dec 13, 2029ActiveRegistration details
- Analysis ID
- 4b2f28f196302a44f324501e277d0cb7
- Customs Code
- DHA09402110007
Company information
- Manufacturer
- DIO CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- DIO IMPLANT TAIWAN CORPORATION
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Dental Bone Implant Operation Equipment (F.3980)" Identification Scope of the First Level.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3980 Intradental implant manipulation equipment
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 13, 2019
- Expiry Date
- Dec 13, 2029
About this record
Access comprehensive regulatory information for "Diou" dental intraosseous implant attachment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4b2f28f196302a44f324501e277d0cb7 and manufactured by DIO CORPORATION. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.
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