"Reesan" Desktop Automatic Chemical Cold Light Immunoassay Analyzer (Unsterilized) - Taiwan Registration d98338581a453d8a4df60c71900f2dc7
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 d98338581a453d8a4df60c71900f2dc7 and manufactured by DIASORIN S.P.A.. 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 Italia SpA, 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 Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.
A Clinical chemistry and clinical toxicology
A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
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Dates and Status
Jan 22, 2021
Jan 22, 2026
Sep 30, 2021
Cancellation Information
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