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Cephus Catheter

Sealcath, LLC · Model 0006560 · UDI-DI 00860000559133

FCE Prescription
10
510(k) clearances
73
Adverse events (2 deaths)
0
Recalls
70
Facilities

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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.