Profile: Cordis Corp., a Johnson & Johnson company develops products to treat circulatory system diseases including congestive heart failure and cerebral aneurysms. Its product lines include the balloons, catheters, forceps, guidewires, and plain and drug-coated stents used in cardiology, endovascular, and neurovascular procedures & also develops medical sensor and electrophysiology technology for cardiovascular use, while its Biologics Delivery Systems division makes cardiac mapping equipment used to improve the delivery of biological therapies. Our NOGA®XP Cardiac Navigation system provide leading-edge evaluation, mapping, and navigation tools to support physicians performing cardiac procedures. Delivering unmatched accuracy in tissue assessment and precise targeting & provide accurate and reliable cardiac visualization and precise navigation within the cardiac space.

The company was founded in 1959, has ~7000 employees. NASDAQ:CORD (SEC Filings)

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• Angiographic Catheter Amplatz Left 1.0

• Angiographic Catheter, Angled Pigtail

• Biliary Stents

• Biopsy Forceps

• Biopsy Forceps Femoral Approach

• Biopsy Forceps, Internal Jugular Approach

• Cardiac Navigation System

• Cardiopulmonary Bypass Pump Tube (FDA Code: DWE / 870.4390) A cardiopulmonary bypass pump tubing is polymeric tubing which is used in the blood pump head and which is cyclically compressed by the pump to cause the blood to flow through the cardiopulmonary bypass circuit.

• Cardiovascular Intravascular Filter (FDA Code: DTK / 870.3375) A cardiovascular intravascular filter is an implant that is placed in the inferior vena cava for the purpose of preventing pulmonary thromboemboli (blood clots generated in the lower limbs and broken loose into the blood stream) from flowing into the right side of the heart and the pulmonary circulation.

• Carotid Stent (FDA Code: NIM)

• Carotid Stent Systems (FDA Code: NIM)

• 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 Sheath Introducers

• Circular Mapping Catheter

• Continuous Flush Catheter (FDA Code: KRA / 870.1210) A continuous flush catheter is an attachment to a catheter-transducer system that permits continuous intravascular flushing at a slow infusion rate for the purpose of eliminating clotting, back-leakage, and waveform damping.

• Coronary Dilation Balloons, Coronary Dilatation Catheter

• Coronary Drug-Eluting Stent (FDA Code: NIQ)

• Coronary Interventions

• Coronary Stent (FDA Code: MAF)

• Diagnostic Biliary Catheter (FDA Code: FGE / 876.5010) A biliary catheter and accessories is a tubular flexible device used for temporary or prolonged drainage of the biliary tract, for splinting of the bile duct during healing, or for preventing stricture of the bile duct. This generic type of device may include a bile collecting bag that is attached to the biliary catheter by a connector and fastened to the patient with a strap.

• Diagnostic Catheter

• Diagnostic Guidewires, Steerable

• 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.

• El Gamal Angiographic Catheter

• Electrode Recording Catheter (FDA Code: DRF / 870.1220) An electrode recording catheter or an electrode recording probe is a device used to detect an intracardiac electrocardiogram, or to detect cardiac output or left-to-right heart shunts. The device may be unipolar or multipolar for electrocardiogram detection, or may be a platinum-tipped catheter which senses the presence of a special indicator for cardiac output or left-to-right heart shunt determinations.

• Embolectomy Catheters (FDA Code: DXE / 870.5150) An embolectomy catheter is a balloon-tipped catheter that is used to remove thromboemboli, i.e., blood clots which have migrated in blood vessels from one site in the vascular tree to another.

• Embolic Injectable Agent (FDA Code: MFE)

• Esophageal Dilators (FDA Code: KNQ / 876.5365) An esophageal dilator is a device that consists of a cylindrical instrument that may be hollow and weighted with mercury or a metal olive-shaped weight that slides on a guide, such as a string or wire and is used to dilate a stricture of the esophagus. This generic type of device includes esophageal or gastrointestinal bougies and the esophageal dilator (metal olive).

• Expandable Metallic Stent

• General & Plastic Surgery Surgical Clamp (FDA Code: GDJ / 878.4800) A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.

• Guide Catheter, Left Coronary Bypass, Type Bypass

• Guide Catheter, Left Coronary Bypass, Type Bypass / Judkins

• Guide Catheter, Left Coronary Bypass, Type Coronary Bypass

• Guide Catheter, Right Coronary Bypass Curve

• Guide Wires, J Tip-Fixed Core

• Guide Wires, J Tip-Movable Core

• Guidewire Catheter (FDA Code: DQX / 870.1330) A catheter guide wire is a coiled wire that is designed to fit inside a percutaneous catheter for the purpose of directing the catheter through a blood vessel.

• Guidewires, Straight Movable Core

• Guidewires, Straight-Fixed Core

• Iliac Stent (FDA Code: NIO)

• Intracranial Neurovascular Stent (FDA Code: NJE)

• Intravascular Radiotherapy, Gamma Rays

• Judkins Catheter

• Neurovascular Embolization Device (FDA Code: HCG / 882.5950)

• Percutaneous Catheter (FDA Code: DQY / 870.1250) A percutaneous catheter is a device that is introduced into a vein or artery through the skin using a dilator and a sheath (introducer) or guide wire.

• Percutaneous Catheterization Vessel Dilator (FDA Code: DRE / 870.1310) A vessel dilator for percutaneous catheterization is a device which is placed over the guide wire to enlarge the opening in the vessel, and which is then removed before sliding the catheter over the guide wire.

• Percutaneous Catheters Sets, Pediatric

• Percutaneous Catheters Sets, Pediatric Percutaneous Access

• Percutaneous Transluminal Coronary Angioplasty Catheter (FDA Code: LOX / 870.5100)

• Peripheral Transluminal Angioplasty Catheter (FDA Code: LIT / 870.1250)