BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    XENON ARC ENDOSCOPE LIGHT SOURCE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110997·DOUBLE PLASTIC STERILIZATION CASE

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867058767·UNIVERS FRACTURE STEM SCREWDRIVER

    SPIDER FLEXIBLE BLUNT DISSECTOR AND BAND PASSER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MODIFICATION TO EBI XFIX DFS OPTIROM ELBOW FIXATOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INTERGRATED APD SET

    FDA Adverse Event
    Malfunction ·VANTIVE US HEALTHCARE LLC·Product code FKX·April 4, 2025

    COLLEAGUE COLOR PUMP CE FRENCHVERSION SINGLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·December 10, 2010

    CAPTURE-R READY-SCREEN (POOLED)

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·January 17, 2013

    IDENTITY ADX XL DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·July 8, 2014