BEUDAMED
    865 results · 96ms · Sources: EU EUDAMED, US FDA

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    SENSOR HEALTH PRODUCTS, INC.

    FDA registration
    SENSOR HEALTH PRODUCTS, INC.·53 products·🇨🇦 Canada

    UNKNOWN VAP CLOSED SUCTION CATHETERS & ACCESSORIES

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code BSY·August 17, 2022

    AMBIT PAIN CONTROL SYSTEM, PIB/PCA

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code FRN·September 18, 2023

    CLOSED SUCTION SYSTEM FOR ADULTS WITH BALLARD TECHNOLOGY

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code BSY·September 7, 2018

    CLOSED SUCTION SYSTEM FOR ADULTS WITH BALLARD TECHNOLOGY

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code BSY·September 7, 2018

    CLOSED SUCTION SYSTEM FOR ADULTS WITH BALLARD TECHNOLOGY

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code BSY·September 7, 2018

    CLOSED SUCTION SYSTEM FOR ADULTS WITH BALLARD TECHNOLOGY

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code BSY·September 10, 2018

    DRX REVOLUTION MOBILE X-RAY SYSTEM

    FDA Adverse Event
    Malfunction ·CARESTREAM HEALTH INC.·Product code IZL·May 23, 2024

    CORTRAK ENTERAL ACCESS SYSTEM

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code KNT·May 3, 2024

    HOMEPUMP C-SERIES

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL - IRVINE·Product code MEB·September 24, 2019

    HOMEPUMP C-SERIES

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL - IRVINE·Product code MEB·September 24, 2019

    CORTRAK 2 ENTERAL ACCESS SYSTEM

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code KNT·December 17, 2025

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 23, 2018

    COULTER® LH 500 INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·June 8, 2011

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·April 4, 2018

    TOSOH AIA-900

    FDA Adverse Event
    Malfunction ·TOSOH HI-TEC·Product code KHO·August 9, 2017

    COULTER AC-T DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·June 10, 2011

    AIA-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·April 11, 2018

    A1A-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·April 9, 2018

    A1A-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·April 6, 2018