BEUDAMED
    41 results · 28ms · Sources: EU EUDAMED, US FDA

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    Solution Set for Epidural Use

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SYNTHES SYNPOR HD POROUS POLYETHYLENE THRER DIMENSIONAL IMPLANTS

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

    MODIFICATION TO RELIADENT DENTAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    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

    UNKNOWN DEPUY ACETABULAR LINER

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code KWA·June 11, 2013

    ORTHO SUMMIT SAMPLE HANDLING SYSTEM

    FDA Adverse Event
    Malfunction ·HAMILTON BONADUZ AG·Product code MMH·July 13, 2011

    WALLFLEX DUODENAL STENT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code MUM·September 11, 2008