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Reasan Desktop Automatic Chemical Cold Light Immunoassay Analyzer (Unsterilized) - Taiwan Registration 76bb6cda7460350520fde86620966b33

Access comprehensive regulatory information for Reasan Desktop Automatic Chemical 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 76bb6cda7460350520fde86620966b33 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. 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.

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76bb6cda7460350520fde86620966b33
Registration Details
Taiwan FDA Registration: 76bb6cda7460350520fde86620966b33
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Device Details

Reasan Desktop Automatic Chemical Cold Light Immunoassay Analyzer (Unsterilized)
TW: ็ฆฎไบžๅฐš ๆกŒไธŠๅž‹ๅ…จ่‡ชๅ‹•ๅŒ–ๅญธๅ†ทๅ…‰ๅ…็–ซๅˆ†ๆžๅ„€(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

76bb6cda7460350520fde86620966b33

DHA084a0000102

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

Dates and Status

Oct 04, 2021

Oct 31, 2025