BEUDAMED
    16 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SLEEPEASY

    FDA Adverse Event
    Injury ·RESPIRONICS INC.·Product code BZD·April 12, 2012

    REMSTAR PLUS M-SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·May 6, 2010

    REMSTAR M SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·November 25, 2009

    M-SERIES DC POWER SUPPLY

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·May 25, 2012

    CAPIOX HEMOCONCENTRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code KDI·March 3, 2016

    CELL-DYN DILUENT/SHEATH

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKL·January 5, 2007

    PROMUS ELEMENT¿ PLUS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·April 11, 2013

    RUSCH SAFETY CLEAR PLUS ENDOTRACHEAL TUBE

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·March 1, 2011

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·September 2, 2014

    REMSTAR PLUS M-SERIES

    FDA Adverse Event
    Death ·RESPIRONICS, INC.·Product code BZD·March 16, 2012

    REMSTAR M SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code BZD·February 24, 2010

    REMSTAR PLUS M

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·May 21, 2010

    REMSTAR PLUS M-SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·December 1, 2010

    CAPIOX RX OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 31, 2024

    CELL-DYN RUBY SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code GKZ·November 10, 2023

    REMSTAR PLUS M-SERIES

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code BZD·May 26, 2011