"Ampli" audiometer and accessories thereof (unsterilized) - Taiwan Registration c777c30028181eed079476eccaad2711
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..
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.
Device Details
Product Details
Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Audiogrammeter (G.1050)".
G ENT Science
G.1050 Audiometer
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Apr 27, 2011
Apr 27, 2021
Aug 15, 2023
Cancellation Information
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