Taiwan FDA registration debd8efc50fee81617c2cbcd5da703b3
"Aurora" Precision attachment (Non-Sterile)
TW: "歐洛拉" 精密接著體 (未滅菌)
Taiwan·Risk Class 1·MD·AVINENT IMPLANT, SYSTEM, S.L.·Registered Mar 04, 2021 – Mar 04, 2026ExpiredRegistration details
- Analysis ID
- debd8efc50fee81617c2cbcd5da703b3
- License Form
- Ministry of Health Medical Device Import No. 022356
- Customs Code
- DHA09402235608
Company information
- Manufacturer
- AVINENT IMPLANT, SYSTEM, S.L.
- Manufacturer Country
- Spain
- Authorized Representative
- PORTLAND BIOTECHNICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Precision Adhesive Body (F.3165)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3165 precision bond
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 04, 2021
- Expiry Date
- Mar 04, 2026
About this record
Access comprehensive regulatory information for "Aurora" Precision attachment (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 debd8efc50fee81617c2cbcd5da703b3 and manufactured by AVINENT IMPLANT, SYSTEM, S.L.. The authorized representative in Taiwan is PORTLAND BIOTECHNICAL CO., LTD..
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