Braemar, Inc.

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Web: http://www.braemarinc.com
E-Mail:
Address: 11481 Rupp Drive, Burnsville, Minnesota 55337, USA
Phone: +1-(952)-890-5135 | Fax: +1-(952)-882-6550 | Map/Directions >>
 
 

Profile: Braemar, Inc. specializes in the engineering, development and manufacturing of ambulatory cardiac monitoring devices. We are accredited with ISO 9001:2000 & ISO 13485 certification. Our products are CE marked. Our product line includes digital holter monitors, cardiac arrhythmia monitors, analog holter recorders and holter cassette playback systems. Our digital devices incorporate the latest software technology to allow seamless integration into PC analysis application. The digital holter provide high quality ECG digital recording with no data compression. Removable Braemar certified compact flash cards for the DL800 and DL1200 make it easy to transfer data. For the DXP, a simplified high speed USB data transfer eliminates additional hardware requirements for your analysis system.

The company was founded in 1998, has revenues of USD 10-25 Million, has ~40 employees and is ISO 9001, CE certified.

FDA Registration Number: 2133409

22 Products/Services (Click for related suppliers)  
• Ambulatory Electrocardiograph (FDA Code: MWJ / 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.
• Ambulatory Electrocardiograph (ECG) Analysis Systems (FDA Code: MLO / 870.2800)
• Anesthetic Infusion Pump (FDA Code: FRN / 880.5725)
An infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manner. The device may use a piston pump, a roller pump, or a peristaltic pump and may be powered electrically or mechanically. The device may also operate using a constant force to propel the fluid through a narrow tube which determines the flow rate. The device may include means to detect a fault condition, such as air in, or blockage of, the infusion line and to activate an alarm.
• 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.
• Blood Flow Probes
• ECG Long-Term Recorder
• Holter ECG Monitors
• Holter ECG Monitors, 24 Hour Holter Monitor
• Holter ECG Monitors, Analog Holter
• Holter ECG Monitors, Cassette Tape Recorder
• Holter ECG Monitors, Digital Compact Flash Holter Recorder
• Holter ECG Monitors, Digital Holter Recorder
• Holter ECG Monitors, ECG System
• Holter ECG Monitors, Holter Heart Monitor
• Medical Magnetic Tape Recorder (FDA Code: DSH / 870.2800)
• Microprocessor Based Electromagnetic Blood Flowmeter
• Peristaltic Infusion Pump (FDA Code: FRN / 880.5725)
• Portable ECG Long-Term Recorder
• Radiofrequency Physiological Transmitter/Receiver System (FDA Code: DRG / 870.2910)
A radiofrequency physiological signal transmitter and receiver is a device used to condition a physiological signal so that it can be transmitted via radiofrequency from one location to another, e.g., a central monitoring station. The received signal is reconditioned by the device into its original format so that it can be displayed.
• Recording ECG Long-Term Scanner
• Research Electromagnetic Blood Flowmeter
• Telephone Single-Channel ECG Transmitter/Receiver System

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