BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    HEMISPHERE ACETABULAR CUP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    P.F.C. SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295233565·P.F.C. SIGMA TIBIAL COMPONENT ALL POLY CURVED 5...

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756025126·Stockinette

    EW200 SYSTEM (OXYGEN SATURATION MONITORING SYSTEM) AND PRESEP OXIMETRY CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Medline Waste Station

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TAXUS® LIBERTÉ®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·February 14, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·January 13, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 28, 2014

    Depuy P.F.C. E Knee System, all polyethylene curved tibial component, Sz 5, 8 mm; Ref 96-0660.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005

    Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 300 mm, Item Number: 814613300

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·September 19, 2018