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LEVELERT

Smith & Nephew, Inc. · Model 7211011 · UDI-DI 03596010556011

FLN Prescription
10
510(k) clearances
15
Adverse events
0
Recalls
3
Facilities

Description

LEVELERT II FLUID LEVEL SENSOR

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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.