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NeMus PC PERIPHERAL

EB NEURO SPA · Model B9800066800 · UDI-DI 08056446900215

JXE GWJ GWF IKN Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

EMG/EP System

Recalls

Date	Firm	Reason
2012-04-18	Biomet, Inc.	Incorrect product picture label was on the product box.

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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.