Taiwan FDA registration 4dadac8fe23e377c7fd7eb342492334f
“AURICA” Hearing Aid (Non-Sterile)
TW: “歐俄聲” 助聽器 (未滅菌)
Taiwan·Risk Class 1·MD·AURICA LTD.·Registered Nov 27, 2020 – Nov 27, 2025ExpiredRegistration details
- Analysis ID
- 4dadac8fe23e377c7fd7eb342492334f
- License Form
- Ministry of Health Medical Device Import No. 022136
- Customs Code
- DHA09402213607
Company information
- Manufacturer
- AURICA LTD.
- Manufacturer Country
- Russian Federation
- Authorized Representative
- YOU FU ELECTRIC DEVELOPMENT CO.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Hearing Aids (G.3300)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G3300 hearing aid
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 27, 2020
- Expiry Date
- Nov 27, 2025
About this record
Access comprehensive regulatory information for “AURICA” Hearing Aid (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 4dadac8fe23e377c7fd7eb342492334f and manufactured by AURICA LTD.. The authorized representative in Taiwan is YOU FU ELECTRIC DEVELOPMENT CO..
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