Profile: Peter Schiff Enterprise are providers of various sizes of intra-aortic balloons with acessories, battery operated AC cardiac fibrillators, electrode cables/pads and various sizes of mechanical ventricular assist cups.
FDA Registration Number: 1044143
9 Products/Services (Click for related suppliers)
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| • AC-Powered Fibrillator (FDA Code: LIW) |
| • Bipolar Electrode Cables |
| • Detachable Needle Electrode Cables & Accessories |
| • 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. |
| • Electrosurgical Electrode Cables |
| • Intra-Aortic Balloon System (FDA Code: DSP / 870.3535) A intra-aortic balloon and control system is a device that consists of an inflatable balloon, which is placed in the aorta to improve cardiovascular functioning during certain life-threatening emergencies, and a control system for regulating the inflation and deflation of the balloon. The control system, which monitors and is synchronized with the electrocardiogram, provides a means for setting the inflation and deflation of the balloon with the cardiac cycle. |
| • Left Ventricular Circulatory Assist Unit (FDA Code: DSQ) |
| • Monopolar Electrode Cables |
| • Tripolar Electrode Cables |