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

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    FORCEPS CLIPRACK VENTRICULAR CANNULA SAWS SPATULAS

    FDA 510(k)
    FDA Class 1 ·Neurology

    EMIT QST ACETAMINOPHEN ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    MICRO-MAT SYSTEM

    FDA 510(k)
    FDA Class 1 ·Hematology

    INTERLOCK?-35

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KRD·June 16, 2014

    ENTRUST AT

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·October 19, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 16, 2012

    SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX

    FDA Enforcement
    Class II ·Completed·Townsend Design·January 17, 2024