BEUDAMED
    8 results · 29ms · Sources: EU EUDAMED, US FDA

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    RADIATION PROTECTION APRON

    FDA 510(k)
    FDA Class 1 ·Radiology

    TROCHANTERIC NAIL KIT, TI GAMMA3 11X200MM X 120

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·January 8, 2013

    DIVERSI-MED STERILE LATEX SURGEON'S GLOVES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    FLO-GARD 6300 DUAL CHANNEL VOLUME INFUSION PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·May 19, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 5, 2012

    TENDRIL DX

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2010

    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