Taiwan FDA registration 7670b63b231801fd5dbf820a7452a415
"Ampfox" Audiotest (Unsterilized)
TW: "安普佛克司" 聽力檢查儀 (未滅菌)
Taiwan·Risk Class 1·AMPLIVOX LTD.·Registered Jun 19, 2020 – Jun 19, 2025ExpiredRegistration details
- Analysis ID
- 7670b63b231801fd5dbf820a7452a415
- Customs Code
- DHA09402164803
Company information
- Manufacturer
- AMPLIVOX LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- JAG MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the "Audiogrammeter (G.1050)" of the Measures for the Classification and Grading Management of Medical Equipment.
- 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
- Jun 19, 2020
- Expiry Date
- Jun 19, 2025
About this record
Access comprehensive regulatory information for "Ampfox" Audiotest (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7670b63b231801fd5dbf820a7452a415 and manufactured by AMPLIVOX LTD.. The authorized representative in Taiwan is JAG MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices