BEUDAMED
    11 results · 33ms · Sources: EU EUDAMED, US FDA

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    WALLSTENT ENTERAL ENDOPROTHESIS

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

    ZenTite (Unicorn+); ZenTite (Unicorn+I); ZenTite (Unicorn+II); ZenTite (Unicorn+III)

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

    MEDSURG AMNIOCENTESIS TRAY

    FDA 510(k)

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·January 9, 2013

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 10, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2014

    VANGUARD CR ILOK FEM-RT 60

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 24, 2020

    COBALT G-HV BONE CEMENT 40G

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·April 21, 2021

    COBALT G-HV BONE CEMENT 40G

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·April 21, 2021

    COBALT G-HV BONE CEMENT 40G

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·April 21, 2021

    1.65 X 5 MM HIGH TORQUE SELF-DRILL CROSS-DRIVE SCREW 5-PACK

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·December 5, 2016