Reasan Automatic cold light immunoassay analyzer (unsterilized) - Taiwan Registration 948389b04ae0cc6ad3476dd8e0b1dc0d
Access comprehensive regulatory information for Reasan Automatic 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 948389b04ae0cc6ad3476dd8e0b1dc0d and manufactured by DiaSorin Italia SpA. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) 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 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
Dates and Status
Oct 05, 2021
Oct 31, 2025