BEUDAMED
    11 results · 31ms · Sources: EU EUDAMED, US FDA

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    NemoCast

    FDA 510(k)
    FDA Class 2 ·Dental

    SAIPH

    FDA UDI
    MATORTHO LTD·05055455506022·SAIPH Femur Cemented Red Left Size 4

    BONASTENT BILIARY

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    AESCULAP- MEITHKE PROGAV PROGRAMMABLE SHUNT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    Versa-Fx®

    FDA UDI
    Zimmer, Inc.·00889024035584·

    PROGAV®

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·January 3, 2018

    SAIPH KNEE

    FDA Adverse Event
    Malfunction ·MATORTHO·Product code JWH·October 9, 2018

    COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 13, 2008

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 27, 2013

    PCS2

    FDA Adverse Event
    Malfunction ·HAEMONETICS CORP.·Product code KSR·July 21, 2011

    TALENT TAA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·July 9, 2013