BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO CAPIOX FLEXIBLE VENOUS RESERVOIR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WAVEWRITER ALPHA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 13, 2022

    QUANTUM, MODELS SR, HR, DL; VASCULIGHT, MODELS SR, HR, VS, VX, DL

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

    CLS VARUS STEM/CLS 135 STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COMPLETE

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code LPN·April 17, 2020

    3.0MM TI CERVICAL SPINE LOCKING SCREW 14MM-STERILE

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code KWQ·February 10, 2020

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·April 22, 2013

    NEW LIGASURE 5MM

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·April 15, 2011

    IMMULITE 2500, TURBO TROPONIN I

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code MMI·July 1, 2008