"Dynex" Disco Clinical Use Enzyme Analyzer (Unsterilized) - Taiwan Registration 7a5cfd61afb9f18394feade8867506a8
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 7a5cfd61afb9f18394feade8867506a8 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 classification and grading management measures of medical equipment "Enzyme Analyzer for Clinical Use (A.2500)" first level identification range.
A Clinical chemistry and clinical toxicology
A.2500 Enzyme analyzer for clinical use
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Oct 01, 2021
Oct 31, 2025