BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    SYNTHES (USA) DISTAL FEMUR PLATE (DFP) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    9.5F PERCU DOUBLE LUMEN INTRA-AORTIC BALLOON

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DETERMIN HEMOGLOBIN ALC/HI PERF LIQ CHROMATOGRAPHY

    FDA 510(k)
    FDA Class 2 ·Hematology

    STYLE 410 COHESIVE SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·August 1, 2023

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 5, 2014

    DEVICE #3- SYNERGIES PLUS NBC1

    FDA Adverse Event
    Malfunction ·DADE BEHRING, INC.·Product code LON·November 1, 2005

    X3 TRIATHLON CS INSERT #5 13MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS LIMERICK·Product code MBH·January 25, 2011