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“EUROIMMUN”Anti-Glutamate receptor (type NMDA) IIFT EUROPattern - Taiwan Registration eab5cf45226450d37a968a4a2a6682cb

Access comprehensive regulatory information for “EUROIMMUN”Anti-Glutamate receptor (type NMDA) IIFT EUROPattern in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eab5cf45226450d37a968a4a2a6682cb 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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eab5cf45226450d37a968a4a2a6682cb
Registration Details
Taiwan FDA Registration: eab5cf45226450d37a968a4a2a6682cb
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Device Details

“EUROIMMUN”Anti-Glutamate receptor (type NMDA) IIFT EUROPattern
TW: “歐蒙”免疫螢光法抗麩胺酸受體抗體優化圖譜檢測試劑
Risk Class 2
MD

Registration Details

eab5cf45226450d37a968a4a2a6682cb

Ministry of Health Medical Device Import No. 032962

DHA05603296200

Product Details

This product is used for in vitro qualitative or semi-quantitative detection of anti-glutamine receptor (NMDA type) antibody immunoglobulin IgG antibody in human serum, plasma or cerebrospinal fluid (CSF) samples. Used to assist in the diagnosis of neurological disorders (encephalitis).

C Immunology and microbiology devices

C5660 Multiple autologous antibody immunoassay system

Imported from abroad

Dates and Status

Nov 13, 2019

Nov 13, 2024