BEUDAMED
    10,000 results · 63ms · Sources: EU EUDAMED, US FDA

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    PUMP CADD MS3

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code FRN·June 12, 2019

    CADD LEGACY PUMP 1.5MG/ML

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·November 14, 2018

    CADD-LEGACY 1 AMBULATORY PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·February 23, 2022

    CADD-LEGACY 1 AMBULATORY PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·February 24, 2022

    CADD-SOLIS VIP AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FRN·October 1, 2025

    CADD MS3 PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·December 20, 2023

    CADD-LEGACY PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·July 23, 2018

    CADD-LEGACY PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·December 13, 2018

    CADD MS3 7400

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL·Product code FRN·February 24, 2016

    CADD-MS 3 AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·July 3, 2018

    MW5077770

    FDA Adverse Event
    Malfunction ·June 11, 2018

    CADD-LEGACY PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·December 13, 2018

    CADD-LEGACY PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·December 13, 2018

    CADD-LEGACY PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·November 14, 2018

    CADD-LEGACY PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·November 14, 2018

    CADD-LEGACY PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·December 3, 2018

    M-LNC-10-NK M-LNCs™ to NK Patient Cable

    FDA UDI
    MASIMO CORPORATION·00843997009690·

    MW5075688

    FDA Adverse Event
    Malfunction ·March 5, 2018

    MW5075143

    FDA Adverse Event
    February 8, 2018

    CADD EXT SET

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code FPA·July 1, 2021