BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    MODIFIED MODEL M1403A TELEMETRY MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Violet Nitrile Powder-Free Patient Examination Glove, Non Sterile

    FDA 510(k)
    FDA Class 1 ·General Hospital

    AB BELT PRO

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TROCHANTERIC NAIL KIT, TI GAMMA3 11X180MM X 130

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 17, 2012

    ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 19, 2016

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 1, 2016

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·December 10, 2010

    INTEGRITY ADX DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·July 8, 2014

    SM104 MSERIES W5TH WHL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·December 7, 2012