Taiwan FDA registration 861e303ee91810e2e69d6f860ca579f3
"HornTech" Hearing aid (Non-Sterile)
TW: "泉泓"助聽器(未滅菌)
Taiwan·Risk Class 1·MD·STARKEY LABORATORIES, INC.·Registered Oct 13, 2014 – Oct 13, 2024ExpiredRegistration details
- Analysis ID
- 861e303ee91810e2e69d6f860ca579f3
- License Form
- Ministry of Health Medical Device Import No. 014560
- Customs Code
- DHA09401456001
Company information
- Manufacturer
- STARKEY LABORATORIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Quanhong Life Technology Co., Ltd
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
- Oct 13, 2014
- Expiry Date
- Oct 13, 2024
About this record
Access comprehensive regulatory information for "HornTech" 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 861e303ee91810e2e69d6f860ca579f3 and manufactured by STARKEY LABORATORIES, INC.. The authorized representative in Taiwan is Quanhong Life Technology Co., Ltd.
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