Taiwan FDA registration 9adc0006a3439e7fa357a144f3c6e2a7
The seventh generation of Cochlear sound processors and accessories for the core series of Cochlear implants
TW: “科利耳”核心系列第七代人工耳蝸聲音處理器及附件
Taiwan·Risk Class 3·COCHLEAR LIMITED·Registered Mar 22, 2020 – Mar 22, 2030ActiveRegistration details
- Analysis ID
- 9adc0006a3439e7fa357a144f3c6e2a7
- Customs Code
- DHA05603339904
Company information
- Manufacturer
- COCHLEAR LIMITED
- Manufacturer Country
- Australia
- Authorized Representative
- Cochlear Taiwan Limited
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.0001 Artificial ear bug implanter
- Import Information
- Input;; 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.
Dates and status
- Registration Date
- Mar 22, 2020
- Expiry Date
- Mar 22, 2030
About this record
Access comprehensive regulatory information for The seventh generation of Cochlear sound processors and accessories for the core series of Cochlear implants in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9adc0006a3439e7fa357a144f3c6e2a7 and manufactured by COCHLEAR LIMITED. The authorized representative in Taiwan is Cochlear Taiwan Limited.
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