Taiwan FDA registration d366a1ce4ea5b905f59a5974f5f2e1b1

"Fengli" hearing aids (unsterilized)

TW: “峰利”助聽器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·PHONAK AG·Registered Jul 21, 2009 – Jul 21, 2019Cancelled
Registration details
Analysis ID
d366a1ce4ea5b905f59a5974f5f2e1b1
Customs Code
DHA04400792502
Company information
Manufacturer
PHONAK AG
Manufacturer Country
Switzerland
Authorized Representative
SHINING REAL EAR 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 Science
Product Type (Level 2)
G.3300 Hearing Aids
Import Information
import
Dates and status
Registration Date
Jul 21, 2009
Expiry Date
Jul 21, 2019
Cancellation Date
Jun 22, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Fengli" hearing aids (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d366a1ce4ea5b905f59a5974f5f2e1b1 and manufactured by PHONAK AG. The authorized representative in Taiwan is SHINING REAL EAR CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PHONAK AG, 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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