"Reesan" Desktop Automatic Chemical Cold Light Immunoassay Analyzer (Unsterilized) - Taiwan Registration 41c139c20f2bc1e10aa29d32aac80cbc
Access comprehensive regulatory information for "Reesan" Desktop Automatic Chemical Cold Light Immunoassay 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 41c139c20f2bc1e10aa29d32aac80cbc and manufactured by DiaSorin Italia SpA. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DIASORIN S.P.A., 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 the "Individual Photometric Chemistry Analyzer for Clinical Use (A.2160)" of the Measures for the Classification and Grading of Medical Devices.
A Clinical chemistry and clinical toxicology
A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Oct 01, 2021
Oct 31, 2026