IMRIS receives CE Mark approval for interventional imaging system



    WINNIPEG, April 30 /CNW/ - IMRIS Inc. (TSX: IM) ("IMRIS" or the
"Company") today announced CE Mark approval for its integrated MR imaging and
x-ray angiography suite that enables physicians to diagnose, intervene,
resolve and confirm the effectiveness of treatment with one integrated system.
With CE Mark approval, IMRIS will immediately commence marketing in Europe of
two products: IMRISNV for stroke management and advanced neurovascular
interventions and IMRIScardio for cardiovascular interventions.
    IMRISNV features a 3T MRI scanner and a bi-plane angiography system
specifically designed to co-exist in the same suite. Patients with acute
ischemic stroke transition seamlessly from MR imaging to intervention without
moving from the table. During and after the intervention, new MR images can be
taken to assess the effectiveness of the treatment. IMRISNV is designed to
shorten transition time between imaging modalities, decrease the overall time
for treatment and improve patient outcomes.
    IMRIScardio features a 1.5T MRI scanner that provides images that can
improve the physician's ability to visualize the cardiovascular system before,
during and after an intervention. With an integrated single-plane angiography
system, IMRIScardio is designed to improve patient outcomes by decreasing the
overall time for cardiovascular interventions and minimizing the patient's
exposure to radiation and contrast media.
    "CE Mark approval of our system represents our first step into the realm
of neurovascular and cardiovascular interventional imaging", stated David
Graves, CEO of IMRIS. "We are excited about launching our technology in Europe
and we are confident that IMRISNV and IMRIScardio will help physicians and
hospitals improve the outcomes of their patients suffering from a wide range
of neurovascular and cardiovascular conditions."

    About CE Mark
    The CE Mark for medical devices is not a quality mark nor is it intended
for consumers. It is a legally binding statement by the manufacturer that
their product has met all of the requirements of the Medical Devices Directive
(MDD 93/42/EEC), In Vitro Diagnostic Device Directive (IVD 98/79/EC) or the
Active Implantable Medical Device Directive (AIMD 90/385/EEC), where
applicable.

    About IMRIS
    IMRIS (TSX: IM) is a global leader in providing fully integrated,
advanced surgical imaging solutions. The company's flagship product,
IMRISneuro, utilizes patented technology that allows a high field MRI scanner
to be moved in to the operating room on demand, providing imaging during the
surgical procedure without compromising patient safety. This unique and
innovative system has been validated by leading neurosurgeons for use in
world-class neuroscience centers. For more information, visit www.imris.com.





For further information:

For further information: Media: Michael Robbie, Director, Marketing,
Tel: (204) 480-7696, Email: mrobbie@imris.com; Investors: Brad Woods, Investor
Relations, Tel: (204) 480-7094, Email: bwoods@imris.com

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IMRIS Inc.

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