Taiwan FDA registration e69abcdcc4cdee05f1a6dbf8ac14dae3
"Hear-only" air-directed hearing aids (unsterilized)
TW: “惟聽”氣導式助聽器(未滅菌)
Taiwan·Risk Class 1·WIDEX A/S·Registered Jul 06, 2012 – Jul 06, 2017CancelledRegistration details
- Analysis ID
- e69abcdcc4cdee05f1a6dbf8ac14dae3
- Customs Code
- DHA04401192109
Company information
- Manufacturer
- WIDEX A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- MADISON MEDICAL INSTRUMENTS CORP.
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 06, 2012
- Expiry Date
- Jul 06, 2017
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Hear-only" air-directed 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 e69abcdcc4cdee05f1a6dbf8ac14dae3 and manufactured by WIDEX A/S. The authorized representative in Taiwan is MADISON MEDICAL INSTRUMENTS CORP..
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