BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    PERSHIELD CPR DEVICE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    XENOMEM WOUND MATRIX

    FDA 510(k)
    FDA Unclassified ·Unknown

    SECURLINE SURGICAL SKIN MARKER 1000

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

    LRG TAP PRI MOD NCK 8DEG 34MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·February 4, 2013

    INFINITI VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·December 17, 2010

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITJ·July 17, 2014