BEUDAMED
    9 results · 37ms · Sources: EU EUDAMED, US FDA

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    DISPOSABLE ANGIOGRAPHY NEEDLE, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 18, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 18, 2024

    BIPOLAR BIOPSY FORCEPS

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

    SINGLE-USE LAPAROSCOPIC SUCTION/IRRIGATION CANNULA

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

    SYNCHRON (R) SYSTEMS CREATININE REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code CGX·July 2, 2011

    ESPRIT

    FDA Adverse Event
    Injury ·SORIN C.R.M., S.R.L.·Product code NVZ·January 10, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 17, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 6, 2014