Taiwan FDA registration 4cf84b61a654f04863fe133404757654
“Cochlear” Baha 6 Max Sound Processor and Accessories
TW: “科利耳”巴哈麥克斯骨傳導聲音處理器
Taiwan·Risk Class 2·MD·COCHLEAR BONE ANCHORED SOLUTIONS AB·Registered Sep 27, 2022 – Sep 27, 2027ActiveRegistration details
- Analysis ID
- 4cf84b61a654f04863fe133404757654
- License Form
- Ministry of Health Medical Device Import No. 035913
- Customs Code
- DHA05603591302
Company information
- Manufacturer
- COCHLEAR BONE ANCHORED SOLUTIONS AB
- Manufacturer Country
- Sweden
- Authorized Representative
- Cochlear Taiwan Limited
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G3300 hearing aid
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 27, 2022
- Expiry Date
- Sep 27, 2027
About this record
Access comprehensive regulatory information for “Cochlear” Baha 6 Max Sound Processor and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4cf84b61a654f04863fe133404757654 and manufactured by COCHLEAR BONE ANCHORED SOLUTIONS AB. The authorized representative in Taiwan is Cochlear Taiwan Limited.
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