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Catheter, Biliary, Reprocessed

FDA product code NML · Class 2 · Gastroenterology, Urology

1
Registered devices
1
Adverse events
1
Recalls
1
510(k) clearances

Devices with this code

Olympus — OLYMPUS Winter & Ibe GmbH

Recent recalls

DateFirmReason
2008-08-08Sterilmed IncSteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted becau

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.