Taiwan FDA registration 0f5df694e2b3b4aca5810928f3b4dce0
"Audix" air-guided hearing aids (unsterilized)
TW: “唯聽”氣導助聽器 （未滅菌）
Taiwan·Risk Class 1·WIDEX A/S·Registered Jul 21, 2006 – Jul 21, 2016CancelledRegistration details
- Analysis ID
- 0f5df694e2b3b4aca5810928f3b4dce0
- Customs Code
- DHA04400494901
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
- Jul 21, 2006
- Expiry Date
- Jul 21, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Audix" 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 0f5df694e2b3b4aca5810928f3b4dce0 and manufactured by WIDEX A/S. The authorized representative in Taiwan is MELODY MEDICAL INSTRUMENTS CORPORATION.
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