BEUDAMED
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    Filters Status: Malfunction ×

    I.V. PUMP

    FDA Adverse Event
    Malfunction ·3M/AVI·July 29, 1994

    AVI

    FDA Adverse Event
    Malfunction ·3M INFUSION THERAPY·Product code FPA·June 18, 1997

    BVI

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL, INC.·Product code HQL·July 10, 2023

    BVI

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL, INC.·Product code HQL·July 25, 2023

    AVI

    FDA Adverse Event
    Malfunction ·3M·Product code FPA·June 3, 1995

    AVI

    FDA Adverse Event
    Malfunction ·3M HEALTH CARE·Product code FRN·March 17, 1998

    BVI VISITEC

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL·Product code HMX·April 11, 2012

    BVI BEAVER6400

    FDA Adverse Event
    Malfunction ·BECTON VISITEC INTERNATIONAL, INC.·Product code GES·February 4, 2013

    BVI BEAVER6600

    FDA Adverse Event
    Malfunction ·BECTON VISITEC INTERNATIONAL, INC.·Product code GES·February 4, 2013

    AVI 200A

    FDA Adverse Event
    Malfunction ·3M INFUSION THERAPY·Product code FRN·December 13, 1996

    BVI CANNULA

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL, INC.·Product code HMX·June 10, 2024

    BVI 9400

    FDA Adverse Event
    Malfunction ·VERATHON·Product code IYO·September 19, 2014

    ACIST CVI

    FDA Adverse Event
    Malfunction ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·June 10, 2022

    BVI 9400

    FDA Adverse Event
    Malfunction ·VERATHON INC.·Product code IYO·September 19, 2014

    AVI 110

    FDA Adverse Event
    Malfunction ·AVI, INC. 3M HEALTHCARE·Product code FRN·August 11, 1993

    AVI SOLUSET

    FDA Adverse Event
    Malfunction ·3M INFUSION THERAPY·Product code FPA·May 9, 1994

    BVI 3000

    FDA Adverse Event
    Malfunction ·VERATHON MEDICAL·Product code ITX·August 2, 2016

    ACIST CVI

    FDA Adverse Event
    Malfunction ·ACIST MEDICAL SYSTEMS·Product code DXT·June 13, 2017

    BVI VISITEC

    FDA Adverse Event
    Malfunction ·BEAVER-VISITEC INTERNATIONAL·Product code HMX·February 20, 2012

    BVI 9600

    FDA Adverse Event
    Malfunction ·VERATHON MEDICAL·Product code ITX·October 15, 2015