“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).
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
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

