Taiwan FDA registration f69d0620fc2418b529c18d521b1fa013

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

TW: "歐帝風" 氣導式助聽器 (未滅菌)

Taiwan·Risk Class 1·MD·AUDIFON GMBH ＆ CO. KG·Registered Dec 13, 2016 – Dec 13, 2021Expired

Registration details

Analysis ID: f69d0620fc2418b529c18d521b1fa013
License Form: Ministry of Health Medical Device Import No. 017273
Customs Code: DHA09401727300

Company information

Manufacturer: AUDIFON GMBH ＆ CO. KG
Manufacturer Country: Germany
Authorized Representative: KING PAX TECHNOLOGY 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: Dec 13, 2016
Expiry Date: Dec 13, 2021

About this record

Access comprehensive regulatory information for "Audifon" 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 f69d0620fc2418b529c18d521b1fa013 and manufactured by AUDIFON GMBH ＆ CO. KG. The authorized representative in Taiwan is KING PAX TECHNOLOGY CO., LTD..

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