Taiwan FDA registration 6aaf8f92bc5f35c18cf62a8342e56d74
"Hear-only" hearing aids (unsterilized)
TW: “惟聽” 助聽器 (未滅菌)
Taiwan·Risk Class 1·WIDEX A/S·Registered Jun 29, 2010 – Jun 29, 2015CancelledRegistration details
- Analysis ID
- 6aaf8f92bc5f35c18cf62a8342e56d74
- Customs Code
- DHA04400895108
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
- Jun 29, 2010
- Expiry Date
- Jun 29, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Hear-only" 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 6aaf8f92bc5f35c18cf62a8342e56d74 and manufactured by WIDEX A/S. The authorized representative in Taiwan is MADISON MEDICAL INSTRUMENTS CORP..
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