BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    SUCTION RETRACTORS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Cabinet

    FDA UDI
    Maquet Critical Care AB·07325710004906·

    ATRICURE CRYO1 CRYO-ABLATION PROBE

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

    Mineral Collagen Composite Bioactive Moldable

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 18, 2014

    HICKMAN DIALYSIS/APHERESIS 13.5 FR. CHRONIC DUAL LUMEN CATHE

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code LJS·October 8, 2010

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 7, 2012

    SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX

    FDA Enforcement
    Class II ·Completed·Townsend Design·January 17, 2024