BEUDAMED
    6 results · 34ms · Sources: EU EUDAMED, US FDA

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    MODIFIED LABELING TO MODEL 9608 ARTERIAL HEMO BLD.

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

    SAF FECAL COLLECTION KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    ALLEIA (TM) ALLERGEN SPECIFIC IGE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    SOFTCLIX ® LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·January 3, 2013

    UNKNOWN DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·November 8, 2010

    MAX PS DCM TIB BRNG 10X63/67MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·June 25, 2014