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Schistosoma IgG ELISA

DRG Instruments Gesellschaft mit beschränkter Haftung · Model EIA-3512 · UDI-DI 04048474035124

GNH Prescription
2
510(k) clearances
1
Adverse events
0
Recalls
15
Facilities

Description

For the qualitative determination of serum or plasma antibodies in humans, primarily IgG, to Schistosoma spp. using the ELISA technique.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.