BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    ADEL 5000

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

    LD304 MATERNITY BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code HDD·May 29, 2015

    MOONEY & CO., INC.

    FDA registration
    MOONEY & CO., INC.·1 product·🇺🇸 United States

    Suture Wires and Wire Loops

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FIBRIN ANALYSIS SYSTEM ENDOLUMINAL BRUSH

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SIMON NITINOL FILTER

    FDA Adverse Event
    Injury ·NITINOL MEDICAL TECHNOLOGIES, INC.·Product code DTK·September 23, 1996

    2800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 13, 2014

    RIA DRIVESHAFT L520

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HTO·February 8, 2013

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 6, 2011