BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    BriefCase

    FDA 510(k)
    FDA Class 2 ·Radiology

    ATLANTIS® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994235732·PLATE 6190072 ANTERIOR CERVICAL 72.5MM

    ATLANTIS® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00763000867973·PLATE 6190072 ANTERIOR CERVICAL 72.5MM

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690196433·AK3 Tibial Instruments Pan

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690195146·AK3 Tibial Instruments Pan Insert

    VENOUS DRAINAGE CANNULA WITH DURAFLO COATING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CRYOTOP(R) SC

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    PLUS SL

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS AG·Product code KWY·October 7, 2008

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013

    MAXGUARD EXTENSION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP·Product code FPA·June 29, 2011