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GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC. · Model B125 Patient Monitor · UDI-DI 00840682124331

NHP DSK CBQ DSB CCK CBR DXN CCL NHO CBS DQA GWQ DRT MHX FLL NHQ BZQ Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

B125 V1 PATIENT MONITOR ATO MODEL

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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.