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GYRUS ACMI

Gyrus ACMI, LLC · Model 290135 · UDI-DI 00821925037731

EPW Prescription
2
510(k) clearances
2
Adverse events
0
Recalls
9
Facilities

Description

SMALL DISPOSABLE "DONUT" HEAD REST NOTE: IF USING THIS PRODUCT IN STERILE FIELD, DRAPE APPROPIATELY (12/PK)

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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.