Minnetronix, Inc.

Address: 1635 Energy Park Drive, St. Paul, Minnesota 55108, USA
Phone: +1-(651)-917-4060 | Fax: +1-(651)-917-4066 | Map/Directions >>

Profile: Minnetronix, Inc. provides high-quality design, engineering, and manufacturing services to medical device companies with software and electronics-based products. We are accredited with ISO 13485:2003 certification and are FDA registered. Our registered trademark is Minnetronix. Our class II and class III medical products include cardiovascular devices, therapeutic devices, point-of-care diagnostic instruments, implantable devices and monitoring equipment. Our projects range in scope from new product medical device design & development, to existing product upgrades, to turnkey contract medical device manufacturing of finished instruments.

FDA Registration Number: 2133810

11 Products/Services (Click for related suppliers)  
• Atherectomy Coronary Catheter (FDA Code: MCX)
• Atherectomy Peripheral Catheter (FDA Code: MCW / 870.4875)
An intraluminal artery stripper is a device used to perform an endarterectomy (removal of plaque deposits from arterisclerotic arteries.)
• Biopsy Instruments (FDA Code: KNW / 876.1075)
A gastroenterology-urology biopsy instrument is a device used to remove, by cutting or aspiration, a specimen of tissue for microscopic examination. This generic type of device includes the biopsy punch, gastrointestinal mechanical biopsy instrument, suction biopsy instrument, gastro-urology biopsy needle and needle set, and nonelectric biopsy forceps. This section does not apply to biopsy instruments that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.
• Biopsy Instruments (FDA Code: KNW / 876.1075)
• Cardiopulmonary Bypass Pump Speed Controller (FDA Code: DWA / 870.4380)
A cardiopulmonary bypass pump speed control is a device used that incorporates an electrical system or a mechanical system, or both, and is used to control the speed of blood pumps used in cardiopulmonary bypass surgery.
• Diagnostic Electromyograph (FDA Code: IKN / 890.1375)
A diagnostic electromyograph is a device intended for medical purposes, such as to monitor and display the bioelectric signals produced by muscles, to stimulate peripheral nerves, and to monitor and display the electrical activity produced by nerves, for the diagnosis and prognosis of neuromuscular disease.
• Electrosurgical Cutting and Coagulation Device (FDA Code: GEI / 878.4400)
An electrosurgical cutting and coagulation device and accessories is a device intended to remove tissue and control bleeding by use of high-frequency electrical current.
• For Ablation Of Cardiac Tissue Surgical Device (FDA Code: OCL / 878.4400)
• Powered Surgical Laser Instrument (FDA Code: GEX / 878.4810)
(1) A carbon dioxide laser for use in general surgery and in dermatology is a laser device intended to cut, destroy, or remove tissue by light energy emitted by carbon dioxide.
• Product Design & Development
• Ultrasound Ablation System And Accessories (FDA Code: NTB / 878.4400)

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