BEUDAMED
    3 results · 24ms · 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 ×

    AXIOM LUMINOS DRF

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code OWB·May 23, 2014

    3.5MM 90-S SERFAS ENERGY SUCTION PROBE

    FDA Adverse Event
    Injury ·STRYKER ENDOSCOPY-SAN JOSE·Product code GEI·February 15, 2013

    ACCU-CHEK FLEXLINK PLUS

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·December 22, 2010