Overview of Ivy Biomedical Systems, Inc.
Founded in 1984, Ivy Biomedical Systems, Inc. is a
privately-held medical device company headquartered in
Branford, Connecticut. The Company designs, develops and
manufactures patient monitors that incorporate leading
edge technology and innovative, market-specific
features. Our highly diversified products are
used to monitor patient vital signs throughout the
healthcare setting. We are the market leader of
specialized cardiac trigger monitors which are used to
synchronize radiographic image acquisition across most
major advanced cardiac imaging modalities; to include
radionuclide, computed tomography (CT), magnetic resonance imaging (MRI), positron
emission tomography (PET), and single photon emission
tomography (SPECT).
Ivy Biomedical is a long-term strategic partner with a
large OEM customer base, providing a broad portfolio of
highly specialized resources from designing and
prototyping to manufacturing, product distribution, and
marketing and clinical education support. The
Company’s products are sold to most of the worlds
leading medical diagnostic imaging manufacturers which
include: GE Healthcare, Philips Medical Systems, Siemens
Medical Solutions, Toshiba Medical Systems, and Hitachi
Medical Systems.
In
addition to being an OEM supplier, Ivy Biomedical markets and sells
its products through a combination of direct operations,
distributor networks, and business partners worldwide.
Ivy Biomedical’s most recent product introductions are the7000 series of Cardiac
Trigger monitors. These products continue Ivy’s
tradition of developing platform products that can be
used as building blocks to implement innovative and
custom hardware and software solutions not currently
available in other products in the market.
Since inception, we have shipped more than
60,000 physiological monitors worldwide. Ivy Biomedical
Systems maintains an ISO 13485 continuous quality
manufacturing system, and designs and manufactures its
products in full compliance with FDA, UL, and the
Medical Device Directive for the CE requirement.