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. The company's highly diversified products are
used to monitor patient vital signs throughout the
healthcare setting. The company is 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), positron
emission tomography (PET), and single photon emission
tomography (SPECT).
The company 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 markets and sells
its products through a combination of direct operations,
distributor networks, and business partners worldwide.
Ivy’s most recent product introductions are the CTM
300 ECG module and the model 3000 series of Cardiac
Trigger monitors. Both 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, the company has shipped more than
45,000 physiological monitors worldwide. IVY Biomedical
Systems maintains an ISO 13485 continuous quality
manufacturing system, and designs / manufactures its
products in full compliance with FDA, UL, and the
Medical Device Directive for the CE requirement.