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

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    SALICYLATE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295235002·P.F.C. SIGMA OVAL-DOME PATELLA 1-PEG TRIAL 35mm

    FONA Pan/Ceph

    FDA 510(k)
    FDA Class 2 ·Dental

    DBX-H HEMOSTATIC DEMINERALIZED BONE MATRIX PUTTY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    14F X 24CM SPLIT STREAM

    FDA Adverse Event
    Malfunction ·MEDCOMP·Product code MSD·February 8, 2013

    TERUMO PERFUSION SYSTEM 8000

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code JOR·January 11, 2011

    LAMITRODE 44

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL- NEUROMODULATION·Product code GZB·July 15, 2014

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020