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FUJIFILM

FUJIFILM CORPORATION · Model P1 · UDI-DI 04547410440768

FFY Prescription
2
510(k) clearances
10
Adverse events
0
Recalls
103
Facilities

Description

This product is used to insert an endotherapy device and to reduce the spread of patient's droplets toward the operator side with the drape and sponge while using an endoscope under the management of a physician 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.