Taiwan FDA registration f96a5580aaa68906d68ffa9d33a934c1
"Soundton" air-guided hearing aids (unsterilized)
TW: “音得通”氣導式助聽器 (未滅菌)
Taiwan·Risk Class 1·INTERTON A/S·Registered Apr 07, 2010 – Apr 07, 2020CancelledRegistration details
- Analysis ID
- f96a5580aaa68906d68ffa9d33a934c1
- Customs Code
- DHA04400868602
Company information
- Manufacturer
- INTERTON A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- Xingxuan Technology 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
- Apr 07, 2010
- Expiry Date
- Apr 07, 2020
- Cancellation Date
- Jan 23, 2019
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Soundton" air-guided 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 f96a5580aaa68906d68ffa9d33a934c1 and manufactured by INTERTON A/S. The authorized representative in Taiwan is Xingxuan Technology Co., Ltd.
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