Taiwan FDA registration f2a5049ce8fecd4ffcf7be30e52396c3

"GN ReSound" Hearing Aid (Non-Sterile)

TW: "瑞聲"助聽器(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·GN RESOUND A/S·Registered Feb 23, 2016 – Feb 23, 2021Expired
Registration details
Analysis ID
f2a5049ce8fecd4ffcf7be30e52396c3
License Form
Ministry of Health Medical Device Import No. 016184
Customs Code
DHA09401618406
Company information
Manufacturer
GN RESOUND A/S
Manufacturer Country
Denmark
Authorized Representative
GREAT SOUND 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
Feb 23, 2016
Expiry Date
Feb 23, 2021
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About this record

Access comprehensive regulatory information for "GN ReSound" 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 f2a5049ce8fecd4ffcf7be30e52396c3 and manufactured by GN RESOUND A/S. The authorized representative in Taiwan is GREAT SOUND CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GN RESOUND A/S, and 1 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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