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“EUROIMMUN” IIFT:Granulocyte Mosaic 13 EUROPattern - Taiwan Registration f97ec31ae33f1a12f53727aa944e1703

Access comprehensive regulatory information for “EUROIMMUN” IIFT:Granulocyte Mosaic 13 EUROPattern in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f97ec31ae33f1a12f53727aa944e1703 and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is EUROIMMUN (SOUTH EAST ASIA) PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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f97ec31ae33f1a12f53727aa944e1703
Registration Details
Taiwan FDA Registration: f97ec31ae33f1a12f53727aa944e1703
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Device Details

“EUROIMMUN” IIFT:Granulocyte Mosaic 13 EUROPattern
TW: “歐蒙” 免疫螢光法抗嗜中性白血球細胞質抗體(ANCA)檢測系統優化圖譜
Risk Class 2
MD

Registration Details

f97ec31ae33f1a12f53727aa944e1703

Ministry of Health Medical Device Import No. 031469

DHA05603146902

Product Details

This product is used for in vitro qualitative or semi-quantitative detection of anti-neutrophil granular leukocyte cytoplasmic IgG antibodies in serum or plasma samples of patients.

C Immunology and microbiology devices

C5660 Multiple autologous antibody immunoassay system

Imported from abroad

Dates and Status

Sep 13, 2018

Sep 13, 2028