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BBQA II

Medion Grifols Diagnostics AG · Model 1 kit · UDI-DI 07640137340582

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510(k) clearances
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Adverse events
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Facilities

Description

For qualitatively testing reactivity of red blood cells, blood grouping and anti-human globulin serums. Not for in vitro diagnostic use. For laboratory use only.

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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.