Medi/Nuclear Corp., Inc.

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Contact: Glenn Samford - Director of Marketing
Web: http://www.medinuclear.com
E-Mail:
Address: 4610 Littlejohn St., Baldwin Park, California 91706, USA
Phone: +1-(626)-960-9822, 800-321-5981 | Fax: +1-(626)-960-8700 | Map/Directions >>

Profile: Medi/Nuclear Corporation, Inc. specializes in the delivery of radioaerosols for pulmonary imaging studies in nuclear medicine. We deal with the development and manufacturing of radioaerosol delivery devices. Our products include Aero/Vent™ line of radioaerosol imaging systems, including the new two-tube Aero/Vent™"Max" & Aero/Vent™ "Jr", Xenon/Master™ patient delivery system & accessories, as well as nuclear medicine and ventilation system supplies. Our Aero/Vent™ "Jr" radioaerosol lung imaging system is a two tube system that can be pole mounted, or used as table top. It has bacteria and HEPA filters. Its features include reduced breathing time, low breathing resistance, low dead space and portability.

The company was founded in 1973, has revenues of USD 1-5 Million, has ~10 employees.

FDA Registration Number: 2050098

7 Products/Services (Click for related suppliers)

• Breathing Mouthpiece (FDA Code: BYP / 868.5620)

A breathing mouthpiece is a rigid device that is inserted into a patient's mouth and that connects with diagnostic or therapeutic respiratory devices.

• Direct Patient Interface Nebulizer (FDA Code: CAF / 868.5630)

A nebulizer is a device intended to spray liquids in aerosol form into gases that are delivered directly to the patient for breathing. Heated, ultrasonic, gas, venturi, and refillable nebulizers are included in this generic type of device.

• Insta/Vent Radioaerosol Systems

• Radioaerosol Lung Imaging Systems

• Radionuclide Rebreathing System (FDA Code: IYT / 892.1390)

A radionuclide rebreathing system is a device intended to be used to contain a gaseous or volatile radionuclide or a radionuclide-labeled aerosol and permit it to be respired by the patient during nuclear medicine ventilatory tests (testing process of exchange between the lungs and the atmosphere). This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Single Patient Dialysate Delivery System (FDA Code: FKP / 876.5820)

A hemodialysis system and accessories is a device that is used as an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and that consists of an extracorporeal blood system, a conventional dialyzer, a dialysate delivery system, and accessories. Blood from a patient flows through the tubing of the extracorporeal blood system and accessories to the blood compartment of the dialyzer, then returns through further tubing of the extracorporeal blood system to the patient. The dialyzer has two compartments that are separated by a semipermeable membrane. While the blood is in the blood compartment, undesirable substances in the blood pass through the semipermeable membrane into the dialysate in the dialysate compartment. The dialysate delivery system controls and monitors the dialysate circulating through the dialysate compartment of the dialyzer.

• Xenon System