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Trinity Biotech

MARDX DIAGNOSTICS, INC. · Model 40-6196P · UDI-DI 05391516747899

GOX
1
510(k) clearances
0
Adverse events
0
Recalls
10
Facilities

Description

B. Pertussis PT/FHA EIA Test System, EIA for the detection of antibody to Bordetella pertussis PT and FHA, 96 Tests

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.