BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    SUMMIT ACETABULAR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PINN CAN BONE SCREW 6.5MMX15MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018

    SUMMIT POR TAPER SZ6 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018

    PINN CAN BONE SCREW 6.5MMX25MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018

    Polystar Selection EDITION HD

    FDA UDI
    Merz Dental GmbH·D7091983014·posteriors; shade A2; size S; upper jaw

    ATLAS SPEEDER HEAD/CERVICAL COIL, MODEL MJAH-137A

    FDA 510(k)
    FDA Class 2 ·Radiology

    uPMR 790

    FDA 510(k)
    FDA Class 2 ·Radiology

    NA

    FDA UDI
    Zimmer, Inc.·00889024218000·

    2520274-2013-10662

    FDA Adverse Event
    Malfunction ·Product code MNI·February 26, 2013

    SPECTRA OPTIA

    FDA Adverse Event
    Malfunction ·TERUMO BCT·Product code LKN·August 6, 2014

    TALENT THORACIC STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·February 7, 2011