BEUDAMED
    90 results · 21ms · Sources: EU EUDAMED, US FDA

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    SYNESCOPE, EASYSCOPE, SYNECOM, HOLTERREADER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Catalyst CSR Shoulder System

    FDA UDI
    CATALYST ORTHOSCIENCE INC.·00851388006180·Glenoid Trial, Left, Medium

    Ocata Anterior Cervical System

    FDA UDI
    Kalitec Direct LLC·B07308K0120020·Driver Shaft, Final Tighten

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0120020·T-Handle, T25, Screw Height Adjuster

    N/A

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024368989·PLAIN BAR 36 INCHES

    ENDOSKELETON® TA

    FDA UDI
    TITAN SPINE, LLC·00191375051329·7 Deg Lordotic, Implant Caddy, Base, Large

    SUREFIT DISPERSIVE ELECTRODE

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

    VIKING OPTIMA GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NOVOPEN

    FDA Adverse Event
    Injury ·NOVO NORDISK A/S, MEDICAL SYSTEMS·Product code FMF·May 1, 2002

    ENTRIFLEX FEEDING TUBE

    FDA Adverse Event
    Malfunction ·THE KENDAL COMPANY·Product code FPD·May 1, 2002

    Titan™

    FDA UDI
    Ascension Orthopedics, Inc.·10381780245339·Titan™ Total Shoulder System Mini Glenoid Pin G...

    HILL-ROM

    FDA Adverse Event
    Other ·HILL-ROM RITTER·Product code FNL·May 17, 2002

    HILL-ROM

    FDA Adverse Event
    Other ·HILL-ROM RITTER·Product code KNC·May 17, 2002

    CA-HP DIALYZER (CA-HP 210)

    FDA Adverse Event
    Malfunction ·NIPRO CORPORATION·Product code FJI·May 14, 2002

    AFFINITY

    FDA Adverse Event
    Other ·HILL-ROM RITTER·Product code KNC·May 17, 2002

    MEDTRONIC

    FDA Adverse Event
    Injury ·MEDTRONIC INC·Product code DTB·October 14, 2002

    ENTRIFLEX FEEDING TUBE

    FDA Adverse Event
    Other ·THE KENDAL COMPANY·Product code FPD·May 1, 2002

    PHERES-FLOW CENTRAL VENOUS CATHETER KIT

    FDA Adverse Event
    Malfunction ·HORIZON MEDICAL PRODUCTS, INC.·Product code MSD·May 16, 2002

    MEDTRONIC

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·June 26, 2002

    SILHOUETTE

    FDA Adverse Event
    Injury ·MAERSK MEDICAL A/S·Product code FPA·July 4, 2002