MESI ABPI MD

MESI d.o.o. · Model ABPIMDD · UDI-DI 03830059850366

JOM Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

The MESI ABPI MD is an automated wireless ankle-brachial index measuring device for screening patients for Peripheral Arterial Disease (PAD/LEAD). The device is intended to perform, view and store ankle-brachial index (ABI) measurements of adult patients –patients in the PAD risk group.

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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.