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Nofafer Human Antigondiformis Immunoglobulin G Enzyme Immunoassay Kit - Taiwan Registration eee607c3c655dda3070a1bac452938e3

Access comprehensive regulatory information for Nofafer Human Antigondiformis Immunoglobulin G Enzyme Immunoassay Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eee607c3c655dda3070a1bac452938e3 and manufactured by GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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Registration Details
Taiwan FDA Registration: eee607c3c655dda3070a1bac452938e3
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Device Details

Nofafer Human Antigondiformis Immunoglobulin G Enzyme Immunoassay Kit
TW: ่ซพๆณ•้ตไบบ้กžๆŠ—ๅผ“ๆผฟ่Ÿฒๅ…็–ซ็ƒ่›‹็™ฝG้…ต็ด ๅ…็–ซๅˆ†ๆžๅฅ—็ต„
Risk Class 2

Registration Details

eee607c3c655dda3070a1bac452938e3

DHA00601730408

Company Information

Product Details

The Norfa Anti-Toxoplasmin Immunoglobulin G Enzyme Immunoassay Kit is used for the qualitative and quantitative detection of anti-Toxoplasma human immunoglobulin G typing antibodies in human serum or plasma.

C Immunology and microbiology

C.3780 ๅผ“ๆผฟ่Ÿฒ่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Aug 31, 2006

Aug 31, 2026