Itamar Medical Inc.

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Web: http://www.itamar-medical.com
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Address: 160 Speen Street, Suite 201, Framingham, Massachusetts 01701, USA
Phone: +1-(888)-748-2627 | Fax: +1-(88)-748-2628 | Map/Directions >>

Profile: Itamar Medical Inc. is a medical signal company engaged in the development of a proprietary non-invasive window to the autonomic nervous system under the brand name of PAT™. Our PAT signal is used in screening, diagnosing various clinical conditions such as coronary artery disease, myocardial ischemia, congestive heart failure, endothelial dysfunction and cheyne-stokes breathing patterns.

FDA Registration Number: 3004719741

14 Products/Services (Click for related suppliers)

• Actigraphy Kit

• Electro Diagnostic Equipment

• General Diagnostic Equipment

• Home Sleep Testing Kit

• Hydraulic Photo-Electric Plethysmograph (FDA Code: JOM / 870.2780)

A hydraulic, pneumatic, or photoelectric plethysmograph is a device used to estimate blood flow in a region of the body using hydraulic, pneumatic, or photoelectric measurement techniques.

• Oximetry

• Programmable Diagnostic Computer (FDA Code: DQK / 870.1425)

A programmable diagnostic computer is a device that can be programmed to compute various physiologic or blood flow parameters based on the output from one or more electrodes, transducers, or measuring devices; this device includes any associated commercially supplied programs.

• Pulse Oximetry

• Pulse Oximetry Device

• Pulse Rate Monitors

• Reprocessed Short Term Spinal Needle (FDA Code: NMR / 868.5150)

An anesthesia conduction needle is a device used to inject local anesthetics into a patient to provide regional anesthesia.

• Respiratory Monitors

• Sleep Disorder Diagnostic Equipment

• Ventilatory Effort Recorder (FDA Code: MNR / 868.2375)

A breathing (ventilatory) frequency monitor is a device intended to measure or monitor a patient's respiratory rate. The device may provide an audible or visible alarm when the respiratory rate, averaged over time, is outside operator settable alarm limits. This device does not include the apnea monitor classified in 868.2377.