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Daisling Lyasan Toxoplasma immunoglobulin G detection reagent and quality control group - Taiwan Registration 416f2b4b0986fe40947df06a74c8c7e0

Access comprehensive regulatory information for Daisling Lyasan Toxoplasma immunoglobulin G 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 416f2b4b0986fe40947df06a74c8c7e0 and manufactured by DIASORIN S.P.A.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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416f2b4b0986fe40947df06a74c8c7e0
Registration Details
Taiwan FDA Registration: 416f2b4b0986fe40947df06a74c8c7e0
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Device Details

Daisling Lyasan Toxoplasma immunoglobulin G detection reagent and quality control group
TW: ๆˆดๆ€ๆž—็ฆฎไบžๅฐšๅผ“ๆผฟ่Ÿฒๅ…็–ซ็ƒ่›‹็™ฝGๆชขๆธฌ่ฉฆๅŠ‘ๅŠๅ“็ฎก็ต„
Risk Class 2
Cancelled

Registration Details

416f2b4b0986fe40947df06a74c8c7e0

DHA00601790600

Company Information

Italy

Product Details

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

C Immunology and microbiology

C.3780 ๅผ“ๆผฟ่Ÿฒ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Feb 06, 2007

Feb 06, 2012

Apr 03, 2014

Cancellation Information

Logged out

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