BEUDAMED
    9 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 Status: Malfunction ×

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·April 25, 2023

    MAESTRO FOOT SWITCH

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 6, 2018

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·November 3, 2023

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 7, 2023

    MAESTRO 4000 POD, 100W

    FDA Adverse Event
    Malfunction ·STELLARTECH RESEARCH CORPORATION·Product code LPB·August 17, 2023

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·October 2, 2023

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·April 15, 2011

    AXSYM DIGOXIN II REAGENT

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·June 12, 2008

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·October 8, 2019