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

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    FortiBridge Anterior Cervical Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383553445·Gutta Percha Points is used to root canal filin...

    BD DISCARDIT II 5 ML SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·April 8, 2020

    THE CORE (CARDIAC OUTPATIENT REALTIME ECG) MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDOWRIST STAPLER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    EQUINOXE REVERSE SHOULDER COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 13, 2023

    ADVANTAGE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 3, 2013

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·June 29, 2011

    OBTRYX SYSTEM - CURVED

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FTL·August 29, 2008

    EAGLE EYE PLATINUM SHORT TIP

    FDA Adverse Event
    Injury ·VOLCANO CORPORATION·Product code OBJ·July 1, 2016

    EAGLE EYE PLATINUM SHORT TIP; EAGLE EYE PLATINUM ST CATHETER

    FDA Adverse Event
    Injury ·VOLCANO CORPORATION·Product code OBJ·July 1, 2016

    EAGLE EYE PLATINUM SHORT TIP; EAGLE EYE PLATINUM ST CATHETER

    FDA Adverse Event
    Injury ·VOLCANO CORPORATION·Product code OBJ·July 1, 2016

    TC Monitor - Transcutaneous Monitor for p02 and pC02, Model #TCM4, (Cutaneous Oxygen Monitor)

    FDA Recall
    Terminated ·Radiometer America Inc·Product code KLK·February 2, 2005