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

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    MODIFICATION TO DYNESYS SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BSN-JOBST GMBH

    FDA registration
    BSN-JOBST GMBH·3 products·🇩🇪 Germany

    Truliant

    FDA UDI
    Exactech, Inc.·10885862608741·

    Truliant

    FDA UDI
    Exactech, Inc.·10885862608796·

    Truliant

    FDA UDI
    Exactech, Inc.·10885862608727·

    Truliant

    FDA UDI
    Exactech, Inc.·10885862608734·

    Truliant

    FDA UDI
    Exactech, Inc.·10885862608789·

    Truliant

    FDA UDI
    Exactech, Inc.·10885862608819·

    Truliant

    FDA UDI
    Exactech, Inc.·10885862608826·

    Truliant

    FDA UDI
    Exactech, Inc.·10885862608802·

    Truliant

    FDA UDI
    Exactech, Inc.·10885862608758·

    Truliant

    FDA UDI
    Exactech, Inc.·10885862608772·

    Truliant

    FDA UDI
    Exactech, Inc.·10885862608765·

    CARDIAC DIAGNOSTIC SYSTEM, MODEL CH2000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HEARTSTREAM FR2 AED, MODEL M3860A,M3861A

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    1043565-2003-00001

    FDA Adverse Event
    Death ·Product code ---·May 13, 2003

    IBP ELB INT. ULNA LRG RGT LNG STM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDC·June 24, 2016

    LAPAROSCOPIC TISSUE MORCLTR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code HET·April 9, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS INNOVATION CENTER - SILICON VALLEY·Product code GEX·March 28, 2011

    FINELINE II

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code DTB·May 8, 2008