Taiwan FDA registration 3ac9e2f6ef4fcc179574195cca65a370
"Sonic AG" Air Conduction Hearing Aid (Non-Sterile)
TW: "索利康" 氣導式助聽器 (未滅菌)
Taiwan·Risk Class 1·MD·SONIC AG·Registered Apr 13, 2015 – Apr 13, 2020CancelledRegistration details
- Analysis ID
- 3ac9e2f6ef4fcc179574195cca65a370
- License Form
- Ministry of Health Medical Device Import No. 015099
- Customs Code
- DHA09401509900
Company information
- Manufacturer
- SONIC AG
- Manufacturer Country
- Denmark
- Authorized Representative
- MERRY FULING CO., LTD., TAIWAN BRANCH (SAMOA)
Product details
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G3300 hearing aid
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 13, 2015
- Expiry Date
- Apr 13, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Sonic AG" Air Conduction 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 3ac9e2f6ef4fcc179574195cca65a370 and manufactured by SONIC AG. The authorized representative in Taiwan is MERRY FULING CO., LTD., TAIWAN BRANCH (SAMOA).
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