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Hemodialysis Catheter Luer End Cap

FDA product code PEH · Class 2 · Gastroenterology, Urology

1,367
Registered devices
9
Adverse events
1
Recalls
2
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2018-02-15Transonic Systems IncThe sterility of the device cannot be assured. There is a potential for an increased risk of infection.

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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.