Alpha Source, Inc.

Address: 6619 W. Calumet Road, Milwaukee, Wisconsin 53223-4186, USA
Phone: +001-(414)-760-2222, 800-654-9845 | Fax: +001-(414)-760-2070 | Map/Directions >>

Profile: Alpha Source, Inc. provides technical product solutions in the health care market. We are accredited with ISO 13485:2003 certification. We supply replacement lamps, xenon lamps, batteries, battery packs, patient cables & leadwires, diagnostic instruments, repair parts, pulse oximeter sensors, x-ray battery systems, fiber optic cables, and surgical headlights. We are the authorized distributor for all Welch Allyn and Heine diagnostic instruments, accessories, parts and repair services.

The company was founded in 1974, has revenues of USD 1-5 Million, has ~20 employees and is ISO 9002, CE certified.

FDA Registration Number: 2246349

48 Products/Services (Click for related suppliers)  
• 3-Channel Electrocardiograph
• 6-Channel Electrocardiograph
• Adjustable Sphygmomanometer
• Aneroid Sphygmomanometer
• 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.
• Automated External Defibrillators (AEDs)
• Automatic External Defibrillator (FDA Code: MKJ / 870.5310)
An automated external defibrillator (AED) is a low-energy device with a rhythm recognition detection system that delivers into a 50 ohm test load an electrical shock of a maximum of 360 joules of energy used for defibrillating (restoring normal heart rhythm) the atria or ventricles of the heart. An AED analyzes the patient's electrocardiogram, interprets the cardiac rhythm, and automatically delivers an electrical shock (fully automated AED), or advises the user to deliver the shock (semi-automated or shock advisory AED) to treat ventricular fibrillation or pulseless ventricular tachycardia.
• Batteries
• Battery
• Battery Analyzer
• Battery-Powered Ophthalmoscope (FDA Code: HLJ / 886.1570)
An ophthalmoscope is an AC-powered or battery-powered device containing illumination and viewing optics intended to examine the media (cornea, aqueous, lens, and vitreous) and the retina of the eye.
• Coin Operated Sphygmomanometer
• Diagnostic Halogen Otoscope, Ophthal Set
• Disposable Anoscope
• Disposable Sigmoidoscope
• Disposable Tungsten Wire Electrode
• Electric Bulbs
• Electrical & Power Protection Kits
• Electro Sphygmomanometer
• Gaseous Phase Carbon-Dioxide Gas Analyzer (FDA Code: CCK / 868.1400)
A carbon dioxide gas analyzer is a device intended to measure the concentration of carbon dioxide in a gas mixture to aid in determining the patient's ventilatory, circulatory, and metabolic status. The device may use techniques such as chemical titration, absorption of infrared radiation, gas chromatography, or mass spectrometry.
• Hearing Aid Batteries and Accessories
• High Energy Battery-Powered Defibrillator (FDA Code: DRK / 870.5300)
A low-energy DC-defibrillator is a device that delivers into a 50 ohm test load an electrical shock of a maximum of 360 joules of energy used for defibrillating (restoring normal heart rhythm) the atria or ventricles of the heart or to terminate other cardiac arrhythmias. This generic type of device includes low energy defibrillators with a maximum electrical output of less than 360 joules of energy that are used in pediatric defibrillation or in cardiac surgery. The device may either synchronize the shock with the proper phase of the electrocardiogram or may operate asynchronously. The device delivers the electrical shock through paddles placed either directly across the heart or on the surface of the body.
• Home Diagnostics, Otoscopes
• Integrated Sphygmomanometer
• Mercury Sphygmomanometer
• Mobile Fluoroscopic X-Ray System (FDA Code: IZL / 892.1720)
A mobile x-ray system is a transportable device system intended to be used to generate and control x-ray for diagnostic procedures. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.
• Mobile Radiographic Unit Battery
• Mobile X-Ray System (FDA Code: IZL / 892.1720)
• Non-Automated Sphygmomanometer
• Otoscope/Ophthal Sets
• Oximetry
• 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.
• Peristaltic Infusion Pump (FDA Code: FRN / 880.5725)
• Pulse Oximetry
• Pulse Oximetry Device
• Rechargeable Batteries For Class Iii Devices (FDA Code: MOY)
• Rechargeable Battery Box (FDA Code: FCO / 876.1500)
An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.
• Replacement Battery Charger for Ultrasonic Nebulizer
• Replacement Bulbs
• Reusable Otoscope Specula
• Sphygmomanometer Aids
• Sphygmomanometers
• Sphygmomanometers
• Uninterruptible (UPS) Power Systems
• Water-based Sphygmomanometer
• Wheelchair Accessories, Battery Charger
• X-Ray Battery Systems

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