Taiwan FDA registration fd54ede8a63954a6ae974306337cce06
"Koschi" air-directed hearing aids (unsterilized)
TW: “科思奇”氣導式助聽器 (未滅菌)
Taiwan·Risk Class 1·COSELGI A/S·Registered May 09, 2013 – May 09, 2023ExpiredRegistration details
- Analysis ID
- fd54ede8a63954a6ae974306337cce06
- Customs Code
- DHA04401300205
Company information
- Manufacturer
- COSELGI A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- CLINICO INC.
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hearing Aids (G3300)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.3300 Hearing Aids
- Import Information
- import
Dates and status
- Registration Date
- May 09, 2013
- Expiry Date
- May 09, 2023
About this record
Access comprehensive regulatory information for "Koschi" 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 fd54ede8a63954a6ae974306337cce06 and manufactured by COSELGI A/S. The authorized representative in Taiwan is CLINICO INC..
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