Taiwan FDA registration 0cea43930fbaf2bef5028520c055d6fe
"Youwang" air-directed hearing aids (unsterilized)
TW: “友旺” 氣導式助聽器(未滅菌)
Taiwan·Risk Class 1·SIEMENS MEDICAL INSTRUMENTS PTE LTD·Registered Mar 06, 2008 – Mar 06, 2018CancelledRegistration details
- Analysis ID
- 0cea43930fbaf2bef5028520c055d6fe
- Customs Code
- DHA04400655809
Company information
- Manufacturer
- SIEMENS MEDICAL INSTRUMENTS PTE LTD
- Manufacturer Country
- Singapore
- Authorized Representative
- YOU WAN MEDICAL EQUEMENT 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 Science
- Product Type (Level 2)
- G.3300 Hearing Aids
- Import Information
- import
Dates and status
- Registration Date
- Mar 06, 2008
- Expiry Date
- Mar 06, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Youwang" 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 0cea43930fbaf2bef5028520c055d6fe and manufactured by SIEMENS MEDICAL INSTRUMENTS PTE LTD. The authorized representative in Taiwan is YOU WAN MEDICAL EQUEMENT CO., LTD..
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