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GYRUS ACMI, INC

Gyrus ACMI, LLC · Model 230559 · UDI-DI 00821925019935

GCM Prescription
1
510(k) clearances
1,495
Adverse events (1 deaths)
0
Recalls
20
Facilities

Description

FIBER OPTIC LIGHT CABLE 8' LONG 4.0 MM DIAMETER

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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.