BEUDAMED
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    Ventis Medical Inc

    FDA registration
    Ventis Medical Inc·2 products·🇺🇸 United States

    Rechargeable Battery for VM-2000

    FDA UDI
    Ventis Medical Inc.·00850070543026·Battery pack for VM-2XXX Series HeroVent Emerge...

    Carry Case

    FDA UDI
    Ventis Medical Inc.·00850070543101·Carry Case for VM-2XXX Series HeroVent Emergenc...

    Flow Sensor Cable

    FDA UDI
    Ventis Medical Inc.·00850070543057·Flow Sensor Cable for VM-2XXX Series HeroVent E...

    Oxygen Enrichment Kit

    FDA UDI
    Ventis Medical Inc.·00850070543118·Oxygen Enrichment Kit for VM-2XXX Series HeroVe...

    HeroVent

    FDA UDI
    Ventis Medical Inc.·00850070543002·The VM-2000 ventilator is intended to provide c...

    Flow Sensor Reusable

    FDA UDI
    Ventis Medical Inc.·00850070543095·Flow Sensor Reusable for VM-2XXX Series HeroVen...

    ETCO2 Sensor

    FDA UDI
    Ventis Medical Inc.·00850070543071·ETCO2 sensor for VM-2XXX Series HeroVent Emerge...

    Flow Sensor

    FDA UDI
    Ventis Medical Inc.·00850070543064·Flow Sensor for VM-2XXX Series HeroVent Emergen...

    A.C Power Supply

    FDA UDI
    Ventis Medical Inc.·00850070543040·A.C Power Supply for VM-2XXX Series HeroVent Em...

    Primary Battery for VM-2000

    FDA UDI
    Ventis Medical Inc.·00850070543019·Battery pack for VM-2XXX Series HeroVent Emerge...

    Inlet Filter for VM-2000

    FDA UDI
    Ventis Medical Inc.·00850070543088·Inlet Filter for VM-2XXX Series HeroVent Emerge...

    Emergency Ventilator Complete Package

    FDA UDI
    Ventis Medical Inc.·00850070543033·Complete package containing VM-2XXX Series Hero...

    HAMILTON-T1

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·June 29, 2024

    CORTRAK 2 ENTERAL ACCESS SYSTEM

    FDA Adverse Event
    Injury ·AVANOS MEDICAL INC.·Product code KNT·March 30, 2020

    LH 500 HEMATOLOGY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·December 1, 2011

    Provent -SR - Sleep Apnea Therapy-SR (standard resistance). Prescription only, Single Use; Packed 30 units per box Manufactured in the USA by Ventus Medical Inc. 1301 Shoreway Road, Suite 425; Belmont, CA 94002 Used in the treatment of obstructive sleep apnea.

    FDA Recall
    Terminated ·Ventus Medical, Inc.·Product code OHP·February 3, 2012

    The Provent Nasal Cannula is a nasal appliance device placed in both nostrils intended to be used for transmission of respiratory airflow signals between the Provent Professional Sleep Apnea Therapy device and physiologic recorders.

    FDA Recall
    Terminated ·Ventus Medical, Inc.·Product code MNR·December 3, 2009

    The DRX-Revolution Mobile X-Ray System is a diagnostic mobile x-ray system utilizing digital radiography (DR) technology. the system consists of a self-contained x-ray generator, image receptor(s), imaging display and software for acquiring medical diagnostic images outside of standard stationary x-ray room. The DRX-Revolution system incorporates a flat-panel detector that can be used wirelessly for exams such as in-bed chest projections. The system can also be used to expose CR phosphor screens or films.

    FDA Recall
    Open, Classified ·Carestream Health, Inc.·Product code IZL·October 2, 2023

    Llins Service & Consulting GmbH

    Authorized representative
    🇩🇪 Germany·39 Manufacturers·556 Devices