Taiwan FDA registration 04834d83836f0d56393968b150cc0120
"DIO" Endosseous dental implant accessories (Non-Sterile)
TW: "帝歐" 牙齒骨內植入物附件 (未滅菌)
Taiwan·Risk Class 1·MD·DIO CORPORATION·Registered Mar 11, 2014 – Mar 11, 2024ExpiredRegistration details
- Analysis ID
- 04834d83836f0d56393968b150cc0120
- License Form
- Ministry of Health Medical Device Import No. 013954
- Customs Code
- DHA09401395401
Company information
- Manufacturer
- DIO CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- DIO IMPLANT TAIWAN CORPORATION
Product details
- Intended Use
- Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3980 Dental Intraosseous Implant Attachment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 11, 2014
- Expiry Date
- Mar 11, 2024
About this record
Access comprehensive regulatory information for "DIO" Endosseous dental implant accessories (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 04834d83836f0d56393968b150cc0120 and manufactured by DIO CORPORATION. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.
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