BEUDAMED
    3 results · 25ms · 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.
    Filters FDA Adverse Event ×

    CESAR OMCP VISUB CCD V5000

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code IZI·December 3, 2010

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    UNKNOWN·Product code ITJ·February 4, 2013

    LANCET DEVICE SNSRTR CMFRT EN

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·July 17, 2014