Taiwan FDA registration e49bb17f5d15a5ed6b15a534ce41670e

"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·Sonova Operation Center Vietnam Co., Ltd·Registered Nov 13, 2017 – Nov 13, 2027Active
Registration details
Analysis ID
e49bb17f5d15a5ed6b15a534ce41670e
License Form
Ministry of Health Medical Device Import No. 018490
Customs Code
DHA09401849000
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
Nov 13, 2017
Expiry Date
Nov 13, 2027
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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 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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