Oscor Inc.

Web: http://www.oscor.com
Address: 3816 De Soto Boulevard, Palm Harbor, Florida 34683, USA
Phone: +1-(727)-937-2511 | Fax: +1-(727)-937-6077 | Map/Directions >>

Profile: Oscor Inc. designs, develops & markets a variety of highly specialized permanent and temporary pacing lead systems. We offer products such as implantable pacing leads, temporary pacing leads, myocardial heart wires, lead adapters, catheters & external pacemakers. Our implantable and temporary pacemaker systems are used to treat cardiac bradyarrhythmias, which has an adult heart rate below 60 beats per minute, and other coronary disorders. Our pace 101 H is an external single chamber cardiac demand pacemaker that has an option for a trial overdrive stimulation.

The company was founded in 1982, has revenues of USD 5-10 Million, has ~130 employees and is ISO 9001, CE certified.

FDA Registration Number: 1035166

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• Active Fixation Atrial Leads
• Active Fixation Atrial Leads, Bipolar
• Active Fixation Atrial Leads, Unipolar
• Active Fixation Defibrillator Leads
• Active Fixation Lead, bipolar
• Active Fixation Lead, Unipolar
• Angiographic Wire Guide
• Balloon Catheters
• Balloon Type Cardiovascular Catheter
• Cardiac Pacemakers
• Cardiovascular Trocar (FDA Code: DRC / 870.1390)
A trocar is a sharp-pointed instrument used with a cannula for piercing a vessel or chamber to facilitate insertion of the cannula.
• Catheter Introducers (FDA Code: DYB / 870.1340)
A catheter introducer is a sheath used to facilitate placing a catheter through the skin into a vein or artery.
• Catheter Introducers, MULLINS
• Catheter Introducers, Mullins Design
• Diagnostic Intravascular Catheter (FDA Code: DQO / 870.1200)
An intravascular diagnostic catheter is a device used to record intracardiac pressures, to sample blood, and to introduce substances into the heart and vessels. Included in this generic device are right-heart catheters, left-heart catheters, and angiographic catheters, among others.
• 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.
• External Pacemaker
• External Pacemaker Pulse Generator (FDA Code: DTE / 870.3600)
An external pacemaker pulse generator is a device that has a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the heart. This device, which is used outside the body, is used as a temporary substitute for the heart's intrinsic pacing sytem until a permanent pacemaker can be implanted, or to control irregular heartbeats in patients following cardiac surgery or a myocardial infarction. The device may have adjustments for impulse strength, duration, R-wave sensitivity, and other pacing variables.
• Flow Directed Catheter (FDA Code: DYG / 870.1240)
A flow-directed catheter is a device that incorporates a gas-filled balloon to help direct the catheter to the desired position.
• Foley Catheter Introducer
• Guidewires
• Implantable Venous Access Catheter Introducer Kits
• Introducer Sets
• Myocardial Heart Wires, Pin Adapter Set
• Myocardial Heartwires
• Pacemaker Generator Function Analyzer (FDA Code: DTC / 870.3630)
A pacemaker generator function analyzer is a device that is connected to a pacemaker pulse generator to test any or all of the generator's parameters, including pulse duration, pulse amplitude, pulse rate, and sensing threshold.
• Pacemaker Lead Adaptor (FDA Code: DTD / 870.3620)
A pacemaker lead adaptor is a device used to adapt a pacemaker lead so that it can be connected to a pacemaker pulse generator produced by a different manufacturer.
• Pacing Lead Adaptors
• Passive Fixation Atrial Leads
• Passive Fixation Atrial Leads, Bipolar
• Passive Fixation Atrial Leads, Uniploar
• Passive Fixation Defibrillator Leads
• Passive Fixation Defibrillator Leads, Bipolar
• Passive Fixation Defibrillator Leads, Dual Coil, Dual Coil
• Passive Fixation Defibrillator Leads, Tripolar
• Passive Fixation Defibrillator Leads, Uni- and bipolar
• Permanent Cardiac Pacemaker (FDA Code: DTB / 870.3680)
A temporary pacemaker electrode is a device consisting of flexible insulated electrical conductors with one end connected to anexternal pacemaker pulse generator and the other end applied to the heart. The device is used to transmit a pacing electrical stimulus from the pulse generator to the heart and/or to transmit the electrical signal of the heart to the pulse generator.
• Permanent Leads Pacing Accessories, Vein Pick VP-01
• Permanent Pacing Leads
• Radiofrequency Lesion Generator (FDA Code: GXD / 882.4400)
A radiofrequency lesion generator is a device used to produce lesions in the nervous system or other tissue by the direct application of radiofrequency currents to selected sites.
• Radiofrequency Lesion Probe (FDA Code: GXI / 882.4725)
A radiofrequency lesion probe is a device connected to a radiofrequency (RF) lesion generator to deliver the RF energy to the site within the nervous system where a lesion is desired.
• Standard Active Fixation Leads
• Standard Passive Fixation Leads
• Steerable Catheter (FDA Code: DRA / 870.1280)
A steerable catheter is a catheter used for diagnostic and monitoring purposes whose movements are directed by a steering control unit.
• Suture sleeve, Ligature Sleeve LS-15
• Suture sleeve, Ligature Sleeve LS-18
• Suture sleeve, Ligature Sleeve LS-24
• Suture sleeve, Ligature Sleeve LS-26
• Temporary Lead with Stylet
• Temporary Pacemaker Electrode (FDA Code: LDF / 870.3680)

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