BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    HOWTEK 960

    FDA 510(k)
    FDA Class 2 ·Radiology

    PK AIM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SMITH & NEPHEW KINSA RC SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·April 29, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 21, 2013

    ZIMMER FEMORAL HEAD

    FDA Adverse Event
    Malfunction ·ZIMMER·Product code JDI·January 4, 2011