Taiwan FDA registration 3d187cc96dc9b2df6fe401487f56178e

"Hearing-only" air-guided hearing aids (unsterilized)

TW: "惟聽" 氣導助聽器 (未滅菌)

Taiwan·Risk Class 1·WIDEX A/S·Registered May 08, 2012 – May 08, 2022Cancelled

Registration details

Analysis ID: 3d187cc96dc9b2df6fe401487f56178e
Customs Code: DHA04401167609

Company information

Manufacturer: WIDEX A/S
Manufacturer Country: Denmark
Authorized Representative: MELODY MEDICAL INSTRUMENTS CORPORATION

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: May 08, 2012
Expiry Date: May 08, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Hearing-only" air-guided 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 3d187cc96dc9b2df6fe401487f56178e and manufactured by WIDEX A/S. The authorized representative in Taiwan is MELODY MEDICAL INSTRUMENTS CORPORATION.

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