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    EQS-Adhoc  498  0 Kommentare LifeWatch AG: FDA clearance for continuous Vital Signs Monitoring Service

    EQS Group-Ad-hoc: LifeWatch AG / Key word(s): Regulatory Approval
    LifeWatch AG: FDA clearance for continuous Vital Signs Monitoring Service

    09.02.2016 / 07:00
    Release of an ad hoc announcement pursuant to Art. 53 KR.
    The issuer is solely responsible for the content of this announcement.

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    LifeWatch(TM) receives FDA clearance for its continuous Vital Signs
    Monitoring Service

    Zug/Switzerland, February 9, 2016 - LifeWatch AG (SIX Swiss Exchange:
    LIFE), a leading developer and provider of medical solutions and remote
    diagnostic monitoring services in the digital health market, is pleased to
    announce that it has received FDA clearance for its continuous Vital Signs
    Monitoring Service.

    The wireless, patch-based vital signs monitoring system makes vital signs
    monitoring faster, easier and more convenient for both, patients and
    medical staff. It will allow for early detection of vital sign changes
    thereby enabling faster interventions as well as increased nursing
    efficiency and higher patient satisfaction.

    The Vital Signs Patch is an easy-to-use cable-free sensor worn on a
    patient's upper chest. It is intended to be used on adult patients in a
    clinical environment for the continuous, non-invasive monitoring of ECG,
    heart rate, respiration rate, surface temperature, arterial blood oxygen
    saturation and body position. It will be available in two versions (with
    and without ECG) and is connected with an easy-to-use wireless supporting
    system, which provides medical information and alerts remotely to medical
    staff. Although the system will initially be used in a medical facility
    (hospital, nursing home, etc.), the even larger ambulatory market should
    follow once the technology has been proven in the clinical environment.

    Dr. Stephan Rietiker, CEO of LifeWatch, stated: "This clearance represents
    another significant technological breakthrough for LifeWatch and further
    strengthens our position as an innovational leader in digital health. I am
    highly excited at the tremendous market potential for the easy-to-use Vital
    Signs Patch, both in the clinical and ambulatory settings worldwide.
    Furthermore, the cost benefits will allow vital signs monitoring to be
    utilized for a much broader patient population. However, providing service
    in a clinical environment is a new market for LifeWatch and will therefore
    require both time and additional resources in order to ensure a successful
    market launch."


    For further questions:

    LifeWatch AG
    c/o Dynamics Group, Philippe Blangey / Doris Rudischhauser
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    EQS-Adhoc LifeWatch AG: FDA clearance for continuous Vital Signs Monitoring Service EQS Group-Ad-hoc: LifeWatch AG / Key word(s): Regulatory Approval LifeWatch AG: FDA clearance for continuous Vital Signs Monitoring Service 09.02.2016 / 07:00 Release of an ad hoc announcement pursuant to Art. 53 KR. The issuer is solely responsible …