BEUDAMED
    6 results · 26ms · Sources: EU EUDAMED, US FDA

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    INJECTION NEEDLE PROBE/DEVICE-TUNIS

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

    TBG 125I RIA KIT, RADIOIMMUNO. OF SERUM THYROXINE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MAXGUARD ADVANCED LUER ACTIVATED DEVICE WITH ANTIMICROBIAL

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·February 28, 2013

    ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 10, 2011

    2.55 MM X 25.4 MM FLUTED ROUTER

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GFF·December 18, 2013