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

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    GROSHONG CV CATHETER REPAIR KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TEMP-A-LERT MODEL TA-986

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ARROW ECHOGENIC INTRODUCER NEEDLE COMPONENT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ANEURX

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·June 13, 2014

    PERMANENT CAUTERY SPATULA INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code NAY·December 11, 2012

    ALARIS PUMP

    FDA Adverse Event
    Other ·CAREFUSION CORP·Product code FRN·June 23, 2015

    OPTETRAK Comprehensive Knee System including OPTETRAK RBK PS Tibial Components. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·October 13, 2021