"Reasan" Automatic Cold Light Immunoassay Analyzer (Unsterilized) - Taiwan Registration 2025307f700917dc03228d1721f749cb
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 2025307f700917dc03228d1721f749cb and manufactured by DIASORIN DEUTSCHLAND GMBH. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including DIASORIN S.P.A., DiaSorin Italia SpA, and 2 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
Input;; QMS/QSD
Dates and Status
Oct 01, 2021
Oct 31, 2022
Feb 01, 2023
Cancellation Information
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"Reasan" Automatic Cold Light Immunoassay Analyzer (Unsterilized)
DiaSorin Italia SpA
6cdd22d4af6bd15054a874b88b498343
1
"Reasan" Automatic Cold Light Immunoassay Analyzer (Unsterilized)
DIASORIN S.P.A.
07a261af4beea75477cc665ace963b32
1