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Nofafer Human Anti-Toxoplasmin Immunoglobulin M Enzyme Immunoassay Set - Taiwan Registration 89b439db09996b62f69c05edf5a067fd

Access comprehensive regulatory information for Nofafer Human Anti-Toxoplasmin Immunoglobulin M Enzyme Immunoassay Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 89b439db09996b62f69c05edf5a067fd and manufactured by GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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89b439db09996b62f69c05edf5a067fd
Registration Details
Taiwan FDA Registration: 89b439db09996b62f69c05edf5a067fd
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Device Details

Nofafer Human Anti-Toxoplasmin Immunoglobulin M Enzyme Immunoassay Set
TW: ่ซพๆณ•้ตไบบ้กžๆŠ—ๅผ“ๆผฟ่Ÿฒๅ…็–ซ็ƒ่›‹็™ฝM้…ต็ด ๅ…็–ซๅˆ†ๆžๅฅ—็ต„
Risk Class 2

Registration Details

89b439db09996b62f69c05edf5a067fd

DHA00601759901

Company Information

Product Details

Qualitative detection of antibodies to the M typing of anti-toxoplasma immunoglobulin in human serum.

C Immunology and microbiology

C.3780 ๅผ“ๆผฟ่Ÿฒ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Nov 06, 2006

Nov 06, 2026