Abstract: A medical electrical lead having a pre-formed atrial portion assuming a distinctive U-shape is disclosed. The U-shaped atrial portion of the lead is configured and dimensioned to cause at least one atrial electrode disposed thereon to be pushed against the right atrial wall or right atrial sinus wall through pushing forces generated by the lead pressing against regions of the heart located near the superior vena cava or the tricuspid valve, and/or through the action of gravity. The lead provides superior coupling of the atrial electrodes thereof to the walls of the right atrium, and may be configured for single pass DDD stimulation of the right atrium and the right ventricle or other portions of the heart such as the coronary sinus or the great cardiac vein.

Abstract: A medical electrical lead and introducer system. The lead is a single pass, dual chamber lead, which features in one embodiment an atrial tine. The introducer system is particularly designed for introduction of single pass, dual chamber lead which has an atrial tine. The introducer system facilitates the introduction of a such lead into a patient's heart while safeguarding the tine from damage due to kinking during lead positioning. The lead is a single pass lead which features an atrial tine while the introducer system is particularly designed for introduction of a such lead into a patient's heart so as to safeguard the tine from damage due to kinking during lead positioning. The lead is designed so as to electrically couple both the atrium and the ventricular chambers of the heart. The lead generally features several lengths each having differing stiffness as well as a pre-formed bend. The lead also features a atrial tine having an electrode at the tip.

Abstract: An introducer system for a lead, catheter, probe or the like, employing a dilator and introducer sheath assembly for dilating a body vessel in preparation for introducing the lead, etc., through the lumen of the introducer sheath that provides for the injection of radiopaque contrast media to observe the cause of an impediment to advancement of the assembly into the vessel lumen. The dilator is formed of an elongated dilator body having a guide wire lumen therein for receiving and being advanced over the guide wire and a hub assembly at the proximal end of the guide wire body. An injection lumen is also formed in the dilator body isolated from the guide wire lumen and in fluid communication with a side port formed in the hub assembly and an injection port formed in the distal end of the dilator body. Preferably, the injection port is formed in a tapered distal end portion of the dilator.

Abstract: A method of modifying the surface characteristics of a substrate, particularly a polymeric material. The method involves grafting ethylenically unsaturated monomers and attaching biomolecules, such as heparin, to the surface of the substrate, such as a polymeric material, in one step using an oxidizing metal, such as ceric ions.