BEUDAMED
    5 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    CUSA EXCEL 23KHZ STRAIGHT HANDPIECE

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES (IRELAND) LIMITED·Product code LFL·May 14, 2014

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 12, 2013

    BV 25

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code IZL·November 10, 2010

    PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code HSX·October 15, 2025

    GENESIS UNI KNEE FEMORAL COMPONENT COCR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code HSX·May 23, 2025