“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).
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
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

