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Daisling Ryasan CMV immunoglobulin M detection reagent and quality control group - Taiwan Registration 954e780df4f954ab41851158fbc5f79a

Access comprehensive regulatory information for Daisling Ryasan CMV immunoglobulin M detection reagent and quality control group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 954e780df4f954ab41851158fbc5f79a and manufactured by DIASORIN S.P.A.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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954e780df4f954ab41851158fbc5f79a
Registration Details
Taiwan FDA Registration: 954e780df4f954ab41851158fbc5f79a
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Device Details

Daisling Ryasan CMV immunoglobulin M detection reagent and quality control group
TW: ๆˆดๆ€ๆž—็ฆฎไบžๅฐšๅทจ็ดฐ่ƒž็—…ๆฏ’ๅ…็–ซ็ƒ่›‹็™ฝMๆชขๆธฌ่ฉฆๅŠ‘ๅŠๅ“็ฎก็ต„
Risk Class 2
Cancelled

Registration Details

954e780df4f954ab41851158fbc5f79a

DHA00601782408

Company Information

Italy

Product Details

Chemical cold light immunoassay (CLIA) technology is used to quantitatively determine hCMV-specific immunoglobulin M antibodies in human serum or plasma samples.

C Immunology and microbiology

C.3175 ๅทจ็ดฐ่ƒž็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Dec 07, 2006

Dec 07, 2016

May 28, 2018

Cancellation Information

Logged out

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