BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GMK PRIMARY TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·May 20, 2026

    GMK PRIMARY TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·November 18, 2024

    BD PHASEAL¿ INFUSION SET (C61)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code LHI·March 6, 2019

    DUROM US ACETABULAR COMPONENT 58/52 R

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KWA·March 14, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·February 11, 2011

    ULTRASITE HORIZON PUMP IV SET

    FDA Adverse Event
    Injury ·B BRAUN MEDICAL INC·Product code FPA·March 10, 2008

    GORE DUALMESH BIOMATERIAL

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code FTL·May 3, 2019

    IMPAX CV OUTBOUND (RESULTS MANAGEMENT 2.08)

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP·Product code LLZ·September 17, 2013