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FUJIFILM

FUJIFILM CORPORATION · Model SB-500/G · UDI-DI 04547410331530

FFY Prescription

510(k) clearances

Adverse events

Recalls

102

Facilities

Description

This product is the suction button used in combination with our endoscope in medical facilities. Do not use this product for any other purpose.

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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.