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"HornTech" Hearing aid (Non-Sterile) - Taiwan Registration 861e303ee91810e2e69d6f860ca579f3

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.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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861e303ee91810e2e69d6f860ca579f3
Registration Details
Taiwan FDA Registration: 861e303ee91810e2e69d6f860ca579f3
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Device Details

"HornTech" Hearing aid (Non-Sterile)
TW: "ๆณ‰ๆณ“"ๅŠฉ่ฝๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

861e303ee91810e2e69d6f860ca579f3

Ministry of Health Medical Device Import No. 014560

DHA09401456001

Company Information

United States

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Hearing Aids (G.3300)".

G ENT device

G3300 hearing aid

Imported from abroad

Dates and Status

Oct 13, 2014

Oct 13, 2024