BEUDAMED
    38 results · 21ms · Sources: EU EUDAMED, US FDA

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    J2A SLA Dental Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDISLIM

    FDA Adverse Event
    Injury ·MEDICREATIONS, LLC·Product code GEX·April 27, 2020

    DIMENSION VISTA ENZYME 1 CALIBRATOR (ENZ 1 CAL - KC310)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CONCORDE CURVE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·February 12, 2019

    INDIGO SYSTEM SEPARATOR D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·April 18, 2018

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·May 29, 2019

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·January 17, 2020

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·December 7, 2018

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·January 29, 2021

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·December 10, 2020

    PENUMBRA SYSTEM JETD REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·June 5, 2019

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·January 25, 2019

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·January 25, 2019

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·July 28, 2020

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·July 29, 2020

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·September 11, 2020

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·September 24, 2019

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 14, 2011

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·June 11, 2013