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ELDON HOME KIT HKA 2511-1

Eldon Biologicals A/S · Model 504-15v07 · UDI-DI 05713494000511

KSZ

510(k) clearances

10,406

Adverse events (6 deaths)

Recalls

Facilities

Description

For self-testing of AB0 and RhD blood groups. Not for use for screening purposes prior to transfusion. Dry format cards for ABO and/or RhD determination for the grouping of stabilized venous blood, capillary blood or washed red cells.

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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.