"Reasan" Automatic Cold Light Immunoassay Analyzer (Unsterilized) - Taiwan Registration 07a261af4beea75477cc665ace963b32
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 07a261af4beea75477cc665ace963b32 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, 2 companies making similar products including DIASORIN DEUTSCHLAND GMBH, 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
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Feb 26, 2019
Feb 26, 2024
Sep 30, 2021
Cancellation Information
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"Reasan" Automatic Cold Light Immunoassay Analyzer (Unsterilized)
DIASORIN DEUTSCHLAND GMBH
2025307f700917dc03228d1721f749cb
1
"Reasan" Automatic Cold Light Immunoassay Analyzer (Unsterilized)
DiaSorin Italia SpA
6cdd22d4af6bd15054a874b88b498343
1

