BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER

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

    OMNIGUIDE BEAMPATH FIBER AND ADAPTER

    FDA Adverse Event
    OMNIGUIDE, INC.·Product code GEX·October 19, 2010

    Dalbo®-PLUS /-Classic /-B /-Z / Profix

    FDA UDI
    Cendres+Métaux SA·07640166514404·Dalbo®-PLUS /-Classic /-B /-Z / Profix Transfer...

    Zimmer

    FDA UDI
    Provision·B504TQ6070701570·

    N/A

    FDA UDI
    STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825017675·Tourniquet Cuff with Sleeve Dual Port, Single B...

    N/A

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024377219·ZIMMER® STERILE DISPOSABLE TOURNIQUET CUFF WITH...

    POWDER FREE LATEX EXAMINATION GLOVES, STERILE WITH PROTEIN CONTENT LABELING CLAIM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TEMPORARY CROWN AND BRIDGE MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    VERCISE GEVIA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code MHY·March 17, 2021

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·April 22, 2013

    IMIMRESTORE ADVANCED RECHARGEABLE

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·April 25, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 9, 2008