BEUDAMED
    14 results · 23ms · Sources: EU EUDAMED, US FDA

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    ANTHEM™ Fracture System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221046154·Unitek(TM) Molar Band General Purpose Wide Hard...

    EXCELART VANTAGE ATLAS, MODEL MRT-1503

    FDA 510(k)
    FDA Class 2 ·Radiology

    SECURIS SPINAL FIXATION

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EKOSONIC ENDOVASCULAR DEVICE, 135X12CM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KRA·February 3, 2023

    EKOSONIC ENDOVASCULAR DEVICE, 135X12CM

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORPORATION·Product code KRA·February 3, 2023

    EKOSONIC ENDOVASCULAR DEVICE, 106X12CM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KRA·March 1, 2023

    CONSULTA CRT-P

    FDA Adverse Event
    Malfunction ·IPG MFG SWITZERLAND·Product code NVZ·October 10, 2014

    PLEURX PLEURAL CATHETER KIT

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code DWM·June 11, 2013

    PINN MAR +4 10D 36IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 8, 2011

    SENSITHERM PROBE

    FDA Adverse Event
    Injury ·FIAB S.P.A.·Product code FLL·July 10, 2023

    EKOSONIC ENDOVASCULAR DEVICE, 106X18CM

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORPORATION·Product code KRA·February 3, 2023

    GMK-HINGE FEMORAL COMPONENT SIZE 2 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·June 28, 2019

    GMK-HINGE FIXED TIBIAL INSERT SIZE 1/26MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·July 12, 2019