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

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    URINARY DIVERSION STENT

    FDA 510(k)
    FDA Unclassified ·Unknown

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526159518·PROTECT.EPI ELBOW SUPPORT GRAY III

    PARAPAC 200D TRANSPORT, MODEL V200D

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    UGEO H70C DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·May 23, 2014

    DEPUY ASR XL FEM IMP SIZE 53

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·November 13, 2012

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·September 8, 2010