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"Phonak" Air Conduction Hearing Aid (Non-Sterile) - Taiwan Registration e49bb17f5d15a5ed6b15a534ce41670e

Access comprehensive regulatory information for "Phonak" Air Conduction 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 e49bb17f5d15a5ed6b15a534ce41670e and manufactured by Sonova Operation Center Vietnam Co., Ltd. The authorized representative in Taiwan is SONOVA TAIWAN PTE LTD..

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including PHONAK OPERATION CENTER VIETNAM CO. LTD., PHONAK AG, and 3 recent registrations in the same category. 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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e49bb17f5d15a5ed6b15a534ce41670e
Registration Details
Taiwan FDA Registration: e49bb17f5d15a5ed6b15a534ce41670e
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Device Details

"Phonak" Air Conduction Hearing Aid (Non-Sterile)
TW: "็‘žๅฃซๅณฐๅŠ›" ๆฐฃๅฐŽๅผๅŠฉ่ฝๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e49bb17f5d15a5ed6b15a534ce41670e

Ministry of Health Medical Device Import No. 018490

DHA09401849000

Company Information

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

Nov 13, 2017

Nov 13, 2027

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