Taiwan FDA registration 59b57255ceb42a93c765eb4b12248a82
"OSSTELL" DIO IDx Dental Handpiece and Accessories (Non-Sterile)
TW: "歐斯德"牙科手機及其附件(未滅菌)
Taiwan·Risk Class 1·MD·Osstell AB·Registered Oct 03, 2018 – Oct 03, 2023ExpiredRegistration details
- Analysis ID
- 59b57255ceb42a93c765eb4b12248a82
- License Form
- Ministry of Health Medical Device Import No. 019672
- Customs Code
- DHA09401967208
Company information
- Manufacturer
- Osstell AB
- Manufacturer Country
- Sweden
- Authorized Representative
- DIO IMPLANT TAIWAN CORPORATION
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment management measures dental handpieces and their accessories (F.4200).
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4200 Dental Handpiece and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 03, 2018
- Expiry Date
- Oct 03, 2023
About this record
Access comprehensive regulatory information for "OSSTELL" DIO IDx Dental Handpiece and 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 59b57255ceb42a93c765eb4b12248a82 and manufactured by Osstell AB. The authorized representative in Taiwan is DIO IMPLANT TAIWAN CORPORATION.
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