Taiwan FDA registration d3fa76a31d9cbf24eaadcf35d8a96c77
"Clearear" sound processor
TW: “可立耳”聲音處理器
Taiwan·Risk Class 2·COCHLEAR BONE ANCHORED SOLUTIONS AB·Registered Jan 20, 2010 – Jan 20, 2025ExpiredRegistration details
- Analysis ID
- d3fa76a31d9cbf24eaadcf35d8a96c77
- Customs Code
- DHA00602054106
Company information
- Manufacturer
- COCHLEAR BONE ANCHORED SOLUTIONS AB
- Manufacturer Country
- Sweden
- Authorized Representative
- CLINICO INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.3300 Hearing Aids
- Import Information
- The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input
Dates and status
- Registration Date
- Jan 20, 2010
- Expiry Date
- Jan 20, 2025
About this record
Access comprehensive regulatory information for "Clearear" sound processor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d3fa76a31d9cbf24eaadcf35d8a96c77 and manufactured by COCHLEAR BONE ANCHORED SOLUTIONS AB. The authorized representative in Taiwan is CLINICO INC..
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