BEUDAMED
    91 results · 34ms · Sources: EU EUDAMED, US FDA

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    East West Wisconsin

    FDA registration
    East West Wisconsin·10 products·🇺🇸 United States

    EAST WEST INSTRUMENTS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    UNKNOWN·Product code ITJ·June 15, 2012

    GE MEDICAL OMNIBED, CARESTATION AND INCUBATOR

    FDA Adverse Event
    Other ·GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES - CRITIKON DE MEXICO S. DE R.L. DE C.V.·Product code FMZ·February 6, 2025

    Terumo Capiox NX19 Oxygenator with Reservoir (east Orientation), Terumo Capiox NX19 Oxygenator with Reservoir (west Orientation), Terumo Capiox NX19 Oxygenator (east Orientation), Terumo Capiox NX19 Oxygenator (west Orientation)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Terumo Capiox NX19 Oxygenator with Reservoir (east orientation ), Terumo Capiox NX19 Oxygenator with Reservoir (west orientation ), Terumo Capiox NX19 Oxygenator (east orientation ), Terumo Capiox NX19 Oxygenator (west orientation)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CNS-6801A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·June 14, 2021

    UNSPECIFIED BD INFUSION SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·September 15, 2023

    UNSPECIFIED BD INFUSION SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·September 15, 2023

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·May 4, 2026

    CNS-6801A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·June 14, 2021

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·February 24, 2020

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·February 24, 2020

    CNS-6201A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·February 18, 2021

    GIRAFFE INCUBATOR

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code FMZ·September 20, 2019

    GIRAFFE INCUBATOR

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code FMZ·September 27, 2019

    STERILE FX15REC W/ 4L RES

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DTZ·December 17, 2018

    GIRAFFE WARMER

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code FMZ·May 16, 2022

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·July 9, 2014

    STERILE FX15REC W/ 4L RES

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DTZ·December 17, 2018