BEUDAMED
    11 results · 26ms · 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.

    TRIAD-EP II, PLATE INPUT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Precept

    FDA UDI
    Nuvasive, Inc.·00887517425959·PRECEPT Screw, 4.5x30mm Fixed

    MAS PLIF

    FDA UDI
    Nuvasive, Inc.·00887517164728·MAS PLIF Screw, 4.5 x 30mm Polyaxial 3Z

    MEGA PLUS MIS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809916495083·Long-arm Multi-Axial Cannulated Screw, Ø4.5 x 3...

    EXTENSION BOX EB200

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BRAIN HEART INFUSION W/6.5% SODIUM CHLORIDE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    SHILEY

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code BTO·September 1, 2010

    LIGAMAX CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 19, 2014

    UNK COONRAD/MORREY ULNAR COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·October 19, 2010

    IMMERSION HYDROBATH

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ILJ·December 22, 2012

    BIOMET StageOne Hip Cement Spacer Mold with Insert, 56 MM, Silicone, Sterile, Item 431183.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020