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"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.

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c777c30028181eed079476eccaad2711
Registration Details
Taiwan FDA Registration: c777c30028181eed079476eccaad2711
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Device Details

"Ampli" audiometer and accessories thereof (unsterilized)
TW: "ๅฎ‰ๆ™ฎๅŠ›" ่ฝๅŠ›ๆชขๆŸฅ่จˆๅŠๅ…ถ้…ไปถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

c777c30028181eed079476eccaad2711

DHA04401026305

Company Information

United Kingdom

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

Logged out

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