Alpine Biomed Corp.

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Contact: Mr. Brad Westcott - President
Web: http://www.alpinebiomed.com
E-Mail:
Address: 17800 Newhope St., Suite B, Fountain Valley, California 92708-1396, USA
Phone: +1-(714)-839-8426, 800-222-0074 | Fax: +1-(714)-839-8429 | Map/Directions >>

Profile: Alpine Biomed Corp. is a designer, manufacturer and distributor of diagnostic equipment & accessories used in gastroenterology & neurology. We offer established Keypoint ® EMG/EP brand and stellate harmonie products. Our neurology products include EMG/EP systems, magnetic stimulators, EEG/sleep system and accessories. The magpro is a complete line of non-invasive magnetic stimulation systems designed for clinical examinations and research applications within neurophysiology, neurology, rehabilitation & psychiatry. These powerful systems are able to deliver magnetic pulses up to 100 pps, single or twin pulse mode, within a magnetic field on the coil type. Our neuro accessories are electrodes for NCS, EP, caps for EEG and cables & miscellaneous supplies. We provide reflux studies, manometry and GI accessories for gastroenterology.

The company was founded in 1994, has revenues of USD 1-5 Million, has ~80 employees and is ISO 13485:2003 certified.

29 Products/Services (Click for related suppliers)

• Air-Charged Catheters

• Battery-Powered Nerve Stimulator (FDA Code: BXN / 868.2775)

An electrical peripheral nerve stimulator (neuromuscular blockade monitor) is a device used to apply an electrical current to a patient to test the level of pharmacological effect of anesthetic drugs and gases.

• Breathing Frequency Monitor (FDA Code: BZQ / 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.

• Cutaneous Electrode (FDA Code: GXY / 882.1320)

A cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., the electroencephalogram) or to apply electrical stimulation.

• Cystometric Gas on Hydraulic Device (FDA Code: FAP / 876.1620)

A urodynamics measurement system is a device used to measure volume and pressure in the urinary bladder when it is filled through a catheter with carbon dioxide or water. The device controls the supply of carbon dioxide or water and may also record the electrical activity of the muscles associated with urination. The device system may include transducers, electronic signal conditioning and display equipment, a catheter withdrawal device to enable a urethral pressure profile to be obtained, and special catheters for urethral profilometry and electrodes for electromyography. This generic type of device includes the cystometric gas (carbon dioxide) device, the cystometric hydrualic device, and the electrical recording cystometer, but excludes any device that uses air to fill the bladder.

• Diagnostic Electromyograph Needle Electrode (FDA Code: IKT / 890.1385)

A diagnostic electromyograph needle electrode is a monopolar or bipolar needle intended to be inserted into muscle or nerve tissue to sense bioelectrical signals. The device is intended for medical purposes for use in connection with electromyography (recording the intrinsic electrical properties of skeletal muscle).

• Diagnostic Spirometer (FDA Code: BZG / 868.1840)

A diagnostic spirometer is a device used in pulmonary function testing to measure the volume of gas moving in or out of a patient's lungs.

• Electrical Gastrointestinal Motility Analyzer (FDA Code: FFX / 876.1725)

A gastrointestinal motility monitoring system is a device used to measure peristalic activity or pressure in the stomach or esophagus by means of a probe with transducers that is introduced through the mouth into the gastrointestinal tract. The device may include signal conditioning, amplifying, and recording equipment. This generic type of device includes the esophageal motility monitor and tube, the gastrointestinal motility (electrical) system, and certain accessories, such as a pressure transducer, amplifier, and external recorder.

• Electrocardiograph Electrode (FDA Code: DRX / 870.2360)

An electrocardiograph electrode is the electrical conductor which is applied to the surface of the body to transmit the electrical signal at the body surface to a processor that produces an electrocardiogram or vectorcardiogram.

• Electrode Cables (FDA Code: IKD / 890.1175)

An electrode cable is a device composed of strands of insulated electrical conductors laid together around a central core and intended for medical purposes to connect an electrode from a patient to a diagnostic machine.

• Electroencephalographs (FDA Code: GWQ / 882.1400)

An electroencephalograph is a device used to measure and record the electrical activity of the patient's brain obtained by placing two or more electrodes on the head.

• Electroencephalography (EEG) Systems

• Electrogastrography System (FDA Code: MYE / 876.1735)

An electrogastrography system (EGG) is a device used to measure gastric myoelectrical activity as an aid in the diagnosis of gastric motility disorders. The device system includes the external recorder, amplifier, skin electrodes, strip chart, cables, analytical software, and other accessories.

• Electromyography Systems

• Esophageal Motility Monitor and Tube (FDA Code: KLA / 876.1725)

• Evoked Response Electrical Stimulator (FDA Code: GWF / 882.1870)

An evoked response electrical stimulator is a device used to apply an electrical stimulus to a patient by means of skin electrodes for the purpose of measuring the evoked response.

• Gastroesophageal Catheters

• GI & Respiratory Endoscopy Workstation

• Hydraulic Cystometric Device (FDA Code: FEN / 876.1620)

• Impedance Catheters

• Magnetic Stimulators

• Manometry Catheters

• Needle Electrode (FDA Code: GXZ / 882.1350)

A needle electrode is a device which is placed subcutaneously to stimulate or to record electrical signals.

• Nerve Conduction Velocity Measurement Device (FDA Code: JXE / 882.1550)

A nerve conduction velocity measurement device is a device which measures nerve conduction time by applying a stimulus, usually to a patient's peripheral nerve. This device includes the stimulator and the electronic processing equipment for measuring and displaying the nerve conduction time.

• Physiological Signal Amplifier (FDA Code: GWL / 882.1835)

A physiological signal amplifier is a general purpose device used to electrically amplify signals derived from various physiological sources (e.g., the electroencephalogram).

• Reflux Recorders

• Single Lumen Hypodermic Needle (FDA Code: FMI / 880.5570)

A hypodermic single lumen needle is a device intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. The device consists of a metal tube that is sharpened at one end and at the other end joined to a female connector (hub) designed to mate with a male connector (nozzle) of a piston syringe or an intravascular administration set.

• Stomach pH Electrode (FDA Code: FFT / 876.1400)

A stomach pH electrode is a device used to measure intragastric and intraesophageal pH (hydrogen ion concentration). The pH electrode is at the end of a flexible lead which may be inserted into the esophagus or stomach through the patient's mouth. The device may include an integral gastrointestinal tube.

• Water-Perfused Catheters