BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    FUJI COMPUTED RADIOGRAPHY SYSTEM FCR 7501

    FDA 510(k)
    FDA Class 2 ·Radiology

    Delta 3300

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO EBI XFIX DFS RAIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN RIGHT HIP NECK

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MEH·January 4, 2013

    VENTRICULAR ASSIST DEVICE (IVAD)

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·November 18, 2010

    5.5 HEALIX ADVANCE BR 3 SUTURE ANCHOR W/ ORTHOCORD

    FDA Adverse Event
    Malfunction ·DEPUY MITEK·Product code MAI·July 2, 2014

    APPLICATION INSTRUMENT FOR STERNAL ZIPFIX

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code JDQ·August 7, 2019

    APPLICATION INSTRUMENT FOR STERNAL ZIPFIX

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code JDQ·February 10, 2020