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

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    1051786-2019-00015

    FDA Adverse Event
    Malfunction ·April 10, 2019

    XPER FLEX CARDIO PHYSIOMONITORING SYSTEM

    FDA Adverse Event
    Injury ·INVIVO, A DIVISION OF PHILIPS MEDICAL SYSTEMS·Product code MWI·April 7, 2023

    XPER FLEX CARDIO PHYSIOMONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·INVIVO CORPORATION·Product code MWI·October 25, 2019

    BILITX LIGHT SOURCE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code LBI·August 23, 2016

    INTELLIVUE X3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·May 23, 2025

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·April 10, 2013

    BIO-PUSHLOCK 4.5MM X 18.5MM

    FDA Adverse Event
    Other ·ARTHREX INC.·Product code MAI·May 22, 2008

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·April 12, 2011

    INTELLIVUE MULTI-MEASUREMENT MODULE X3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·May 19, 2026

    EXPRESSION PATIENT MONITOR (MR200)

    FDA Adverse Event
    Death ·INVIVO, A DIVISION OF PHILIPS MEDICAL SYSTEMS·Product code MWI·September 16, 2022

    PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KRR·October 15, 2025

    PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KRR·October 20, 2025

    PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KRR·October 15, 2025

    INVIVO CORPORTAION

    FDA Adverse Event
    Injury ·INVIVO CORPORATION·Product code MWI·September 17, 2009

    INVIVO CORPORATIONI

    FDA Adverse Event
    Injury ·INVIVO CORPORATION·Product code MHX·September 17, 2009

    INVIVO CORPORATION

    FDA Adverse Event
    Injury ·INVIVO CORPORATION·Product code MWI·December 2, 2009

    EXPRESSION PATIENT MONITOR (MR400)

    FDA Adverse Event
    Malfunction ·INVIVO, A DIVISION OF PHILIPS MEDICAL SYSTEMS·Product code MWI·September 5, 2023

    INVIVO CORPORATION

    FDA Adverse Event
    Injury ·INVIVO CORPORATION·Product code MWI·December 2, 2009