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

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    PULMONARY ARTERY FLOW-DIRECTED THERMODILUTION CATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIGHT-TOUCH AND SURGI LIGHT FIBERS

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

    PROGRAMMABLE AUDITORY COMPARATOR, MODIFICATION

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

    VIKING

    FDA Adverse Event
    Malfunction ·LIKO AB·Product code FSA·January 11, 2013

    32MM STANDARD FEMORAL HEAD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·November 29, 2010

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 7, 2014

    CIRCUIT PED 5FT DUAL-HTD 20/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code BZE·June 1, 2012

    BD BACTEC FX, INSTRUMENT TOP, PACKAGED

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·February 22, 2021