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.