BEUDAMED
    10 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    01-3801

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·April 27, 2011

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Injury ·KYPHON, INC.·Product code NDN·June 23, 2006

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Injury ·KYPHON, INC.·Product code NDN·June 20, 2006

    MECHANICAL CHAIR/TRANSPORT CHAIR

    FDA Adverse Event
    GOODBABY·Product code INM·March 20, 2013

    NA

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code FOZ·February 4, 2011

    SILICONE ADVANCED OPTIC LENS

    FDA Adverse Event
    Injury ·BAUSCH & LOMB·Product code HQL·March 14, 2008

    SIDUS STEM-FREE SHOULDER, HUMERAL HEAD, 42-15

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSD·June 26, 2018

    SAF-T-INTIMA IV CATHETER SAFETY SYSTEM WITH PRN ADAPTER

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·April 2, 2019

    BD SAF-T-INTIMA¿ IV CATHETER SAFETY SYSTEM

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·May 2, 2019

    SIDUS STEM-FREE SHOULDER, HUMERAL HEAD, 50-21

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSD·June 11, 2018