BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    ACUFEX ENDOBUTTON SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024

    BARD(R) MONOPTY(R) DISPOSABLE CORE BIOPSY INSTRUMENT, BARD(R) MAX-CORE(R) DISPOSABLE CORE INSTRUMENT

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

    MICROSCAN DRIED GRAM-NEGATIVE MIC/COMBO PANELS (GEMIFLOXACIN)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·August 8, 2024

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 30, 2013

    DEPUY ASR PINNACLE TOTAL HIP POROUS LT HIP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC·Product code LPH·December 16, 2010

    ZIPTIGHT

    FDA Adverse Event
    Malfunction ·BIOMET, INC.·Product code MBI·July 2, 2014