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Pocket EEG Device

CERIBELL, INC. · Model C100 · UDI-DI 00851420007052

OMBGWQOMC Prescription
2
510(k) clearances
36
Adverse events (1 deaths)
1
Recalls
13
Facilities

Recalls

DateFirmReason
2021-12-02Natus Neurology DBA Excel Tech., Ltd. (XLTEK)Tile kits that allow one to install and situate a video camera within a patient environment are not fitting properly in some domestic institution ceiling tile grids that have a thi

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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.