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

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    UNIVERSAL CONNECTOR CATALOG NO. 48-1025-5

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

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756714808·ULTRASOUND BIOPSY PACK

    LABEL, STERILIZATION INDICATOR; RADIATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    FC-101 FEMORAL CATHETER GUIDE WIRE

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

    STEAM STER LOCKS ORANGE

    FDA Adverse Event
    Injury ·AESCULAP INC·Product code KCT·October 12, 2016

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·June 26, 2014

    ANTHEM RF

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·November 10, 2010

    AVS ARIA 8DEGX22X55X10 CAGE

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code NKB·December 28, 2012

    STEAM STER LOCKS ORANGE

    FDA Adverse Event
    Malfunction ·AESCULAP INC·Product code KCT·July 26, 2016