BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Affix IIS Spinous Process Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PEGASUS BIOLOGICS ORTHADAPT SURGICAL MESH

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

    CITIEFFE-TITANIUM CANNULATED SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·October 6, 2014

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·June 3, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·June 29, 2011

    TRU CC FEMORAL SIZE 4 LEFT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 6, 2024

    UNKNOWN PATELLA COMPONENT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 6, 2024