BEUDAMED
    28 results · 36ms · Sources: EU EUDAMED, US FDA

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    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·March 31, 2023

    RADOVAN TISSUE EXPANDER, 700 CC

    FDA Adverse Event
    MENTOR CORP.·Product code LCJ·December 21, 1993

    HIGH PROFILE, 400 CC

    FDA Adverse Event
    MCGHAN MEDICAL CORP.·Product code FTR·December 21, 1993

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·June 9, 2021

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·June 9, 2021

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·May 18, 2021

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·May 18, 2021

    LUMIRADX SARS-COV-2 AG TEST STRIP KIT

    FDA Adverse Event
    Malfunction ·LUMIRADX UK LTD.·Product code QKP·May 18, 2021

    CARDIOSAVE HYBRID, TYPE G PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·July 18, 2024

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·November 13, 2024

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·April 28, 2023

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·January 31, 2023

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·May 1, 2023

    CARDIOSAVE HYBRID TYPE J PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·January 25, 2023

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·February 3, 2023

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·November 14, 2024

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·March 8, 2013

    TRIO MOBILE SURGY PLTFRM 2/08

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·February 3, 2011

    TRIATHLON CEMENTED PS FEMORAL COMPONENT #7 RIGHT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·February 19, 2008

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·April 23, 2025