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

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    Perifix and Contiplex Catheter

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ARTHROCARE 8000S COBLATOR SURGERY SYSTEM

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

    REDONDO-L

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ELECTRODE, PACEMAKER, PERMANENT

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·June 8, 2013

    ROTATABLE SNARE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FDI·August 21, 2008

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·September 8, 2008

    ELEKTA LIMITED Elekta Synergy Platform, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear

    FDA Enforcement
    Class II ·Ongoing·Elekta, Inc.·December 13, 2023