BEUDAMED
    7 results · 38ms · Sources: EU EUDAMED, US FDA

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    AUTODOSE INFUSION SYSTEM, MODEL AD4120, BE4210, S12050,100,200, FF0005, 10

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CO2 LASER SYSTEMS & ARTHROGUIDE CO2 LASER FIBER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    LEVITRONIX CENTRIMAG PRIMARY AND BACKUP CONSOLES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AVAULTA PLUS SYNTHETIC SUPPORT SYSTEM: POSTERIOR

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON)·Product code FTL·March 4, 2013

    EON MINI IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 13, 2011

    ADAPTA SR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NVZ·August 8, 2014

    WALLSTENT? RP ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 21, 2025