BEUDAMED
    13 results · 23ms · Sources: EU EUDAMED, US FDA

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    BROOK LIFE SAVING AIRWAY DEVICE #900 &

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172971109·

    SMITH & NEPHEW GLOBAL FEMORAL HEAD TRIALS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Rhinolaryngoscope system

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

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·May 14, 2013

    PINNACLE SECTOR II CUP 52MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·May 14, 2013

    SUMMIT POR TAPER SZ4 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·May 14, 2013

    PINN CAN BONE SCREW 6.5MMX20MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code NDJ·May 14, 2013

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·May 14, 2013

    HEARTSTART FR3 ECG, BASIC BUNDLE, JAPAN

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·March 27, 2014

    TECNIS

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code MFK·November 14, 2012

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 10, 2015

    LOGIC FEMORAL PS CEM LEFT SZ 2

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 5, 2023