Taiwan FDA registration d5a4c9fec0ebb9edaa3c2e418591fc80
“Amplivox” Portable Tympanometer and accessories
TW: “安普佛克司”攜帶式聽阻檢查儀及其配件
Taiwan·Risk Class 2·MD·AMPLIVOX LTD.·Registered Dec 07, 2016 – Dec 07, 2026ActiveRegistration details
- Analysis ID
- d5a4c9fec0ebb9edaa3c2e418591fc80
- License Form
- Ministry of Health Medical Device Import No. 029099
- Customs Code
- DHA05602909903
Company information
- Manufacturer
- AMPLIVOX LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- JAG MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G1090 Hearing Impaired Tester
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 07, 2016
- Expiry Date
- Dec 07, 2026
About this record
Access comprehensive regulatory information for “Amplivox” Portable Tympanometer 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 d5a4c9fec0ebb9edaa3c2e418591fc80 and manufactured by AMPLIVOX LTD.. The authorized representative in Taiwan is JAG MEDICAL CO., LTD..
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