BEUDAMED
    4 results · 19ms · 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 ×

    MULTI SPECT 2 [510(K) K913630]

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SYSTEMS·Product code IYX·April 13, 2001

    ULTRASCAN B

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECH CTR·Product code IYO·June 11, 2014

    8CM ANGLE ATTACHMENT

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·January 10, 2013

    UNICEL® DXC 800 PRO SYNCHRON® CLINICAL SYSTEMS

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·December 6, 2010