"Dynex" Disco Clinical Use Enzyme Analyzer (Unsterilized) - Taiwan Registration 0d44cc9c420363d5b2ed07f2b946a939
Access comprehensive regulatory information for "Dynex" Disco Clinical Use Enzyme Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0d44cc9c420363d5b2ed07f2b946a939 and manufactured by DYNEX TECHNOLOGIES INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DYNEX TECHNOLOGIES INC., and 1 recent registrations in the same category. 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 identification range of enzyme analyzer for clinical use (A.2500) of the Measures for the Administration of Medical Devices.
A Clinical chemistry and clinical toxicology
A.2500 Enzyme analyzer for clinical use
Input;; QMS/QSD
Dates and Status
May 12, 2015
May 12, 2025
Sep 30, 2021
Cancellation Information
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