BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    UNO Negative Pressure Wound Therapy System

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

    Regatta Lateral System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981158040·Lateral Implant, 18mm x 8mm x 40mm, 0 Deg

    Regatta Lateral System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981158057·Lateral Implant, 18mm x 8mm x 40mm, 10 Deg

    BD INSULIN SYRINGE WITH BD ULTRA-FINE NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·June 11, 2019

    LIAC

    FDA 510(k)
    FDA Class 2 ·Radiology

    EMBO PLUS EMBOLECTOMY CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDEAVOR RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·August 15, 2018

    ENDEAVOR RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·August 15, 2018

    CORNERSTONE-SR CAGE SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code ODP·June 20, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·July 7, 2011

    WALLSTENT ENDOPROSTHESIS ENDOSCOPIC BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·September 23, 2008

    TREK¿

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code LOX·January 7, 2026