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"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..

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c21cddd0d60fdb1fe5c2987f1c8b0b8f
Registration Details
Taiwan FDA Registration: c21cddd0d60fdb1fe5c2987f1c8b0b8f
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Device Details

"Reashan" Automatic Cold Light Immunity Analyzer (Unsterilized)
TW: โ€œ็ฆฎไบžๅฐšโ€ ๅ…จ่‡ชๅ‹•ๅ†ทๅ…‰ๅ…็–ซๅˆ†ๆžๅ„€(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

c21cddd0d60fdb1fe5c2987f1c8b0b8f

DHA08402180102

Company Information

Italy

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