Taiwan FDA registration 5fd1a222a5145f38c8cf002071b45fa4

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

TW: "優利康" 氣導式助聽器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·UNITRON HEARING GMBH·Registered Apr 14, 2015 – Apr 14, 2020Cancelled
Registration details
Analysis ID
5fd1a222a5145f38c8cf002071b45fa4
License Form
Ministry of Health Medical Device Import No. 015107
Customs Code
DHA09401510709
Company information
Manufacturer Country
Switzerland
Product details
Product Type (Level 1)
G ENT device
Product Type (Level 2)
G3300 hearing aid
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 14, 2015
Expiry Date
Apr 14, 2020
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Unitron" 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 5fd1a222a5145f38c8cf002071b45fa4 and manufactured by UNITRON HEARING GMBH. The authorized representative in Taiwan is MERRY FULING CO., LTD., TAIWAN BRANCH (SAMOA).

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including SONOVA AG, Sonova Operation Center Vietnam Co., Ltd, and 2 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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