BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    KAB SYSTEM

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    Bonvadis®

    FDA 510(k)
    FDA Unclassified ·Unknown

    OSTEOPORE PCL SCAFFOLD

    FDA 510(k)
    FDA Class 2 ·Neurology

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    GENTEEL HOMECARE PRODUCTS·Product code ITJ·February 8, 2013

    UNICEL® DXC 600 PRO SYNCHRON ® CHEMISTRY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·January 6, 2011

    ENDOVIVE? JEJUNAL FEEDING TUBE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code KNT·July 22, 2014

    Exactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number 314-13-23, c) 44, 47, 50, 53 head, Large, Item Number 314-13-24, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-13-25; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024