BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    TENDERLETT FINGER

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

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111062·INSTRUMENT CASE MEDIUM ALUMINUM

    ARCHITECT C8000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·December 7, 2021

    ECHELON POROUS PLUS HA HIP STEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IB CLINIC

    FDA 510(k)
    FDA Class 2 ·Radiology

    LIGACLIP** ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·December 13, 2010

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    BLUE MAX BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code FGE·March 25, 2006

    ARCHITECT C4000

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code JJE·January 21, 2022