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EPAD

SAFEOP SURGICAL, INC. · Model EPAD · UDI-DI 00851641007145

IKNGWF Prescription
10
510(k) clearances
111
Adverse events (2 deaths)
1
Recalls
69
Facilities

Description

EPAD Stim blue left short cable

Recalls

DateFirmReason
2010-01-29SpineMatrix IncA full design review of the CERSR system was conducted in 7/2009. The audit revealed numerous design verification tests that either did not pass or did not meet the design input r

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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.