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Anti-Strongyloides ELISA (IgG)

EUROIMMUN Medizinische Labordiagnostika AG · Model EI 2290-9601 G · UDI-DI 04049016131601

MDT
0
510(k) clearances
0
Adverse events
1
Recalls
17
Facilities

Recalls

DateFirmReason
2020-04-22BIOSENSE WEBSTERMapping Catheter can become entrapped in the cardiac valvular apparatus while the user is attempting to create an electroanatomic map.

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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.