Taiwan FDA registration c777c30028181eed079476eccaad2711
"Ampli" audiometer and accessories thereof (unsterilized)
TW: "安普力" 聽力檢查計及其配件 (未滅菌)
Taiwan·Risk Class 1·AMPLIVOX LTD.·Registered Apr 27, 2011 – Apr 27, 2021CancelledRegistration details
- Analysis ID
- c777c30028181eed079476eccaad2711
- Customs Code
- DHA04401026305
Company information
- Manufacturer
- AMPLIVOX LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- RONAMAC INTERNATIONAL CORP.
Product details
- Intended Use
- Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Audiogrammeter (G.1050)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.1050 Audiometer
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Apr 27, 2011
- Expiry Date
- Apr 27, 2021
- Cancellation Date
- Aug 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ampli" audiometer and accessories thereof (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c777c30028181eed079476eccaad2711 and manufactured by AMPLIVOX LTD.. The authorized representative in Taiwan is RONAMAC INTERNATIONAL CORP..
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