Taiwan FDA registration 3d19e6fe747bb32e99704642881fd8ff
"INTERTON" Hearing Aid (Non-Sterile)
TW: "德音"助聽器(未滅菌)
Taiwan·Risk Class 1·MD·INTERTON (GN RESOUND AS)·Registered Mar 04, 2016 – Mar 04, 2021ExpiredRegistration details
- Analysis ID
- 3d19e6fe747bb32e99704642881fd8ff
- License Form
- Ministry of Health Medical Device Import No. 016228
- Customs Code
- DHA09401622800
Company information
- Manufacturer
- INTERTON (GN RESOUND AS)
- Manufacturer Country
- Denmark
- Authorized Representative
- GREAT SOUND 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 device
- Product Type (Level 2)
- G3300 hearing aid
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 04, 2016
- Expiry Date
- Mar 04, 2021
About this record
Access comprehensive regulatory information for "INTERTON" Hearing Aid (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3d19e6fe747bb32e99704642881fd8ff and manufactured by INTERTON (GN RESOUND AS). The authorized representative in Taiwan is GREAT SOUND CO., LTD..
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