BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    HEATED INSTRUMENT BATH

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LM-Dental 870276

    Device
    EU MDR · Eu Md Class 1 ·LM-Instruments Oy·Not intended for eu market

    Safety Blood Collection Device for Single Use

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MODIFICATION TO PASSMED SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 12, 2014

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 11, 2010

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·December 12, 2012

    NV GXL LINR, NTRL, 36MM ID, GROUP 4 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·October 26, 2023

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·June 18, 2024

    6.5MM ACETABULAR BONE SCREW 20MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·June 18, 2024