Taiwan FDA registration c60b5ad32952698ec301e68963db48af

"Phonak" Air Conduction Hearing Aid (Non-Sterile)

TW: "瑞士峰力" 氣導式助聽器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·PHONAK OPERATION CENTER VIETNAM CO. LTD.·Registered Jul 14, 2017 – Jul 14, 2022Expired
Registration details
Analysis ID
c60b5ad32952698ec301e68963db48af
License Form
Ministry of Health Medical Device Import No. 018062
Customs Code
DHA09401806202
Company information
Manufacturer Country
Viet Nam
Authorized Representative
SONOVA TAIWAN PTE 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
Jul 14, 2017
Expiry Date
Jul 14, 2022
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About this record

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 c60b5ad32952698ec301e68963db48af and manufactured by PHONAK 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 AG, Sonova Operation Center Vietnam Co., Ltd, 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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