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

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    SR 301 MEDICAL X-RAY FILM

    FDA 510(k)
    FDA Class 1 ·Radiology

    Planmed Clarity 2D and Clarity S

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEROYAL NON-STERILE LOCKING COMPRESSION PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MANUAL ORTHOPEDIC SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·May 6, 2014

    ASR 300 SPIKED CUP SIZE 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·October 16, 2012

    MARQUIS DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·August 11, 2010

    PINN MAR +4 10D 36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·October 28, 2019

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·October 30, 2019