Profile: Guidant Puerto Rico B.V. manufactures ablation systems, cardiac off pump surgical stabilizers, cutting devices, dissection cannula and catheter products. We also supply various dilators, lead adapters and pacemaker accessories.
FDA Registration Number: 2648729
18 Products/Services (Click for related suppliers)
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| • Automatic Implantable Cardioverter Defibrillator With Cardiac Resynchronization (FDA Code: NIK) |
| • Automatic Implantable Cardioverter-defibrillator (FDA Code: LWS) |
| • Cardiopulmonary Bypass Adaptor (FDA Code: DTL / 870.4290) A cardiopulmonary bypass adaptor, stopcock, manifold, or fitting is a device used in cardiovascular diagnostic, surgical, and therapeutic applications to interconnect tubing, catheters, or other devices. |
| • Cardiopulmonary Bypass Oxygenator (FDA Code: DTZ / 870.4350) A cardiopulmonary bypass oxygenator is a device used to exchange gases between blood and a gaseous environment to satisfy the gas exchange needs of a patient during open-heart surgery. |
| • Cardiovascular Surgical Instrument (FDA Code: DWS / 870.4500) Cardiovascular surgical instruments are surgical instruments that have special features for use in cardiovascular surgery. These devices include, e.g., forceps, retractors, and scissors. |
| • Catheter Stylets (FDA Code: DRB / 870.1380) A catheter stylet is a wire that is run through a catheter or cannula to render it stiff. |
| • 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. |
| • Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes (FDA Code: NVN) |
| • Drug-Eluting Permanent Defibrillator Electrodes (FDA Code: NVY) |
| • Dual Chamber Implantable Pulse-Generator (FDA Code: LWP) |
| • 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. |
| • Implantable Pacemaker Pulse Generator With Cardiac Resynchronization (FDA Code: NKE) |
| • 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. |
| • Pacemaker Programmer (FDA Code: KRG / 870.3700) A pacemaker programmer is a device used to change noninvasively one or more of the electrical operating characteristics of a pacemaker. |
| • 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. |
| • 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. |
| • Programmable Implantable Heart Pacemaker (FDA Code: DXY / 870.3610) An implantable 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 is used as a substitute for the heart's intrinsic pacing system to correct both intermittent and continuous cardiac rhythm disorders. This device includes triggered, inhibited, and asynchronous devices implanted in the human body. |
| • Single Single Chamber Pulse-Generator (FDA Code: LWW) |