Taiwan FDA registration f7ea422bf5669b1be2b14d11f505baaa
"Dreve" Biolon Preformed Tooth Positioner (Non-Sterile)
TW: "德瑞芙" 百歐隆成形牙齒固定器(未滅菌)
Taiwan·Risk Class 1·MD·DREVE DENTAMID GMBH·Registered Aug 22, 2019 – Aug 22, 2024ExpiredRegistration details
- Analysis ID
- f7ea422bf5669b1be2b14d11f505baaa
- License Form
- Ministry of Health Medical Device Import No. 020789
- Customs Code
- DHA09402078903
Company information
- Manufacturer
- DREVE DENTAMID GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MNM BIOTECHNOLOGY CO., LTD
Product details
- Intended Use
- Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Shaped Tooth Retainers (F.5525)".
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F5525 Forming Teeth Retainers
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 22, 2019
- Expiry Date
- Aug 22, 2024
About this record
Access comprehensive regulatory information for "Dreve" Biolon Preformed Tooth Positioner (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 f7ea422bf5669b1be2b14d11f505baaa and manufactured by DREVE DENTAMID GMBH. The authorized representative in Taiwan is MNM BIOTECHNOLOGY CO., LTD.
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