BEUDAMED
    7 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SENZA HFX IMPLANT OMNIA SCS SYSTEM

    FDA Adverse Event
    Injury ·NEVRO CORP.·Product code LGW·September 29, 2023

    UROSKOP OMNIA MAX

    FDA Adverse Event
    Injury ·SIEMENS HEALTHCARE GMBH·Product code OWB·March 28, 2023

    EMBRACE GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·OMNIS MEDICAL·Product code NBW·January 14, 2010

    DOSI-FUSER

    FDA Adverse Event
    Malfunction ·LEVENTON/OMNI MEDICAL SUPPLY·Product code MEB·October 10, 2017

    RADIONICS

    FDA Adverse Event
    Malfunction ·OMNI MEDICAL·Product code GXD·June 23, 2000

    SILENT GUARD BALL VALVE

    FDA Adverse Event
    Injury ·AMERICAN OMNI MEDICAL·Product code LWQ·May 15, 1995

    RETROGUARD (STERILE)

    FDA Adverse Event
    Malfunction ·AMERICAN OMNI MEDICAL, INC.·Product code MJJ·January 14, 1999