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Adrenaline ELISA

DRG Instruments Gesellschaft mit beschränkter Haftung · Model EIA-1908 · UDI-DI 00404847419085

CHQ Prescription
10
510(k) clearances
0
Adverse events
0
Recalls
2
Facilities

Description

Manual and automated enzyme immunoassay for the in vitro diagnostic quantitative determination of adrenalin (epinephrine) in human plasma and urine.

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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.