Lifewatch Services, Inc.

Contact: Brent Atwood - EVP Marketing & Sales
Address: O'hare International Center II, 10255 West Higgins Rd., Ste. 100, Rosemont, Illinois 60018, USA
Phone: +1-(847)-720.2100 | Fax: +1-(847)-720-2111 | Map/Directions >>

Profile: Lifewatch Services, Inc. is a provider of ambulatory cardiac event monitors, which are used for receiving software and other ambulatory tools for physicians & medical institutions, enabling professionals to diagnose & treat potentially life-threatening arrhythmia conditions at the earliest possible opportunity. We offer a comprehensive platform of innovative technologies and services that help physicians and users detect & analyze symptoms before they become major health problems. Our CG-6108 ACT wireless cardiac telemetry system is a 1 and 3 channel ECG designed for remote arrhythmia monitoring in any location. A small transmitter worn on the patient sends the ECG data to a portable hand-held device where it is analyzed.

The company was founded in 1993. SWF:CARDG (SEC Filings)

FDA Registration Number: 3027765

18 Products/Services (Click for related suppliers)  
• Ambulatory Cardiac Telemetry System
• Arrhythmia Detector and Alarm (FDA Code: DSI / 870.1025)
The arrhythmia detector and alarm device monitors an electrocardiogram and is designed to produce a visible or audible signal or alarm when atrial or ventricular arrhythmia, such as premature contraction or ventricular fibrillation, occurs.
• Continuous Electronic Thermometer (FDA Code: FLL / 880.2910)
A clinical electronic thermometer is a device used to measure the body temperature of a patient by means of a transducer coupled with an electronic signal amplification, conditioning, and display unit. The transducer may be in a detachable probe with or without a disposable cover.
• Devices For Telemedicine
• EHR Platforms
• Electrocardiograph Transmitter/Receiver System (FDA Code: DXH / 870.2920)
A telephone electrocardiograph transmitter and receiver is a device used to condition an electrocardiograph signal so that it can be transmitted via a telephone line to another location. This device also includes a receiver that reconditions the received signal into its original format so that it can be displayed. The device includes devices used to transmit and receive pacemaker signals.
• Glucose Oxidase, Glucose (FDA Code: CGA / 862.1345)
A glucose test system is a device intended to measure glucose quantitatively in blood and other body fluids. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, neonatal hypoglycemia, and idiopathic hypoglycemia, and of pancreatic islet cell carcinoma.
• Looping Cardiac Event Monitors
• Medical Magnetic Tape Recorder (FDA Code: DSH / 870.2800)
A medical magnetic tape recorder is a device used to record and play back signals from, for example, physiological amplifiers, signal conditioners, or computers.
• Non-Invasive Blood-Pressure Measurement System (FDA Code: DXN / 870.1130)
A noninvasive blood pressure measurement system is a device that provides a signal from which systolic, diastolic, mean, or any combination of the three pressures can be derived through the use of tranducers placed on the surface of the body.
• Over-The-Counter Blood Glucose Test System (FDA Code: NBW / 862.1345)
• Oximeters (FDA Code: DQA / 870.2700)
An oximeter is a device used to transmit radiation at a known wavelength(s) through blood and to measure the blood oxygen saturation based on the amount of reflected or scattered radiation. It may be used alone or in conjunction with a fiberoptic oximeter catheter.
• Patient Monitoring Systems
• Perinatal Monitoring System (FDA Code: HGM / 884.2740)
A perinatal monitoring system is a device used to show graphically the relationship between maternal labor and the fetal heart rate by means of combining and coordinating uterine contraction and fetal heart monitors with appropriate displays of the well-being of the fetus during pregnancy, labor, and delivery. This generic type of device may include any of the devices subject to 884.2600, 884.2640, 884.2660, 884.2675, 884.2700, and 884.2720. This generic type of device may include the following accessories: Central monitoring system and remote repeaters, signal analysis and display equipment, patient and equipment supports, and component parts.
• Spirometry Peak Flow Meter (FDA Code: BZH / 868.1860)
A peak-flow meter for spirometry is a device used to measure a patient's maximum ventilatory flow rate.
• Telemedicine Service
• 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.
• Wireless Healthcare System

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