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Vitex immunoassay group Toxoplasma antibody IgM reagent - Taiwan Registration 42a776077aea2401a2886c601dc495fc

Access comprehensive regulatory information for Vitex immunoassay group Toxoplasma antibody IgM reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 42a776077aea2401a2886c601dc495fc and manufactured by ORTHO-CLINICAL DIAGNOSTICS. The authorized representative in Taiwan is DKSH TAIWAN LTD..

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42a776077aea2401a2886c601dc495fc
Registration Details
Taiwan FDA Registration: 42a776077aea2401a2886c601dc495fc
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Device Details

Vitex immunoassay group Toxoplasma antibody IgM reagent
TW: ็ถญ็‰นๅธๅ…็–ซๆชข้ฉ—่ฉฆๅŠ‘็ต„ๅผ“ๆผฟ่ŸฒๆŠ—้ซ”IgM่ฉฆๅŠ‘
Risk Class 2

Registration Details

42a776077aea2401a2886c601dc495fc

DHA00601994109

Company Information

United Kingdom

Product Details

For in vitro qualitative detection of Toxoplasma gondii antibody IgM in human serum and plasma (heparin, EDTA, or sodium citrate).

A Clinical Chemistry and Clinical Toxicology;; C Immunology and Microbiology

A.1150 ๆ กๆญฃๅ“;; C.3780 ๅผ“ๆผฟ่Ÿฒ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Feb 09, 2009

Feb 09, 2029