BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    UROLOGICAL CATHETER & ACCESSORIES

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

    MULTI DOPPLEX, MD-1

    FDA 510(k)
    FDA Class 2 ·Radiology

    RABBIT MOBILE STANDING FRAME

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 28, 2013

    UNKNOWN DEPUY SMARSET MV ENDURANCE CEMENT

    FDA Adverse Event
    Injury ·DEPUY CMW·Product code LOD·December 14, 2010

    SENSOR ENLITE

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OZO·July 12, 2014

    Allura Xper FD20; Model Numbers: (1) 722006, (2) 722012, (3) 722028; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·October 8, 2025