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

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    SMR Hybrid Glenoid System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Unity Total Knee System

    FDA UDI
    CORIN LTD·05056139233227·Unity ASC Tibial Insert Trials Size 7 to 9 9-14...

    SORB+HISORB+CARTRIDGE

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

    AG MASS

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

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·January 2, 2025

    PLUM XL PUMP

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·October 30, 2008

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·August 26, 2011

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·July 17, 2013

    INJECTOR LOCKING N40-O

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·September 15, 2021

    BD PHASEAL OPTIMA INJECTOR (N40-O)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·September 14, 2021

    INJECTOR LOCKING N40-O

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·September 21, 2021