"Reashan" Automatic Cold Light Immunity Analyzer (Unsterilized) - Taiwan Registration c21cddd0d60fdb1fe5c2987f1c8b0b8f
Access comprehensive regulatory information for "Reashan" Automatic Cold Light Immunity 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 c21cddd0d60fdb1fe5c2987f1c8b0b8f and manufactured by DIASORIN S.P.A.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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.
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
Input;; QMS/QSD
Dates and Status
Oct 01, 2021
Oct 31, 2025

