BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    OXYGEN SENSING DEVICE, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BioSiCar Silicone Implant

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    CARDIOBLATE SURGICAL ABLATION PEN, MODEL 60811C; CARDIOBLATE SURGICAL ABLATION GENERATOR, MODEL 60880

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

    PHILIPS CPAP DEVICE

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·November 4, 2022

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 14, 2014

    12/14 ARTICUL 40MM M SPEC+1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·January 14, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 3, 2010