Biotronik GmbH & Co.

Address: Woermannkehre 1, Berlin D-12359, Germany
Phone: +49-(30)-689-050 | Fax: +49-(30)-6844060 | Map/Directions >>

Profile: Biotronik GmbH & Co. manufactures medical products for the electrotherapy of the heart and vascular intervention. Our astron pulsar self-expanding stent utilises technology in stent conception to create a device that ensures flexibility & improved vessel wall scaffolding. Our Pheron® offers a level of resistance, as well as handling characteristics to provide a level of performance across all aspects of percutaneous transluminal angioplasty.

The company was founded in 1963, has ~3600 employees.

FDA Registration Number: 9610139
US Agent: Jon Brumbaugh / Biotronik, Inc.
Phone: +1-(503)-451-8310  Fax: +1-(503)-451-8519  E-Mail:

46 Products/Services (Click for related suppliers)  
• Ablation System
• Active Fixation Atrial Leads
• Automatic Implantable Cardioverter-defibrillator (FDA Code: LWS)
• Balloon Catheters
• Cardiac CryoAblation Devices
• Cardiac Defibrillators
• Cardiac Pacemaker Generators
• Cardiovascular Catheters
• Catheter Dilator (FDA Code: GCC / 878.4200)
An introduction/drainage catheter is a device that is a flexible single or multilumen tube intended to be used to introduce nondrug fluids into body cavities other than blood vessels, drain fluids from body cavities, or evaluate certain physiologic conditions. Examples include irrigation and drainage catheters, pediatric catheters, peritoneal catheters (including dialysis), and other general surgical catheters. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into the body. Examples of accessories include adaptors, connectors, and catheter needles.
• Coronary Stainless Steel Stents
• Defibrillator Testers (FDA Code: DRL / 870.5325)
A defibrillator tester is a device that is connected to the output of a defibrillator and is used to measure the energy delivered by the defibrillator into a standard resistive load. Some testers also provide waveform information.
• Defibrillators
• Drug-Eluting Permanent Defibrillator Electrodes (FDA Code: NVY)
• Dual-Chamber Implantable Defibrillator (FDA Code: MRM)
• Esophageal Balloon Catheters
• External Pacemaker Electrode
• 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.
• General Purpose Electrosurgical Equipment
• 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
• Heart Pacemaker Generators
• Implantable Cardiac Defibrillators
• Implantable Cardioverter Defibrillators
• Implantable Defibrillators
• Implantable Endocardial Pacemaker Lead
• Implantable Pacemaker Pulse Generator With Cardiac Resynchronization (FDA Code: NKE)
• Implantable Permanent Pulse Generator (FDA Code: NVZ)
• Internal Defibrillators
• Non-Programmable Implantable Heart Pacemaker
• Pacemaker Electrode Function Tester (FDA Code: DTA / 870.3720)
A pacemaker electrode function tester is a device which is connected to an implanted pacemaker lead that supplies an accurately calibrated, variable pacing pulse for measuring the patient's pacing threshold and intracardiac R-wave potential.
• Pacemaker Generators
• 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.
• Passive Fixation Atrial Leads, Bipolar
• Passive Fixation Defibrillator Leads
• Passive Fixation Defibrillator Leads, Bipolar
• Passive Fixation Defibrillator Leads, Tripolar
• 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.
• Peripheral Transluminal Angioplasty Catheter (FDA Code: LIT / 870.1250)
• 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 Pacemaker Generators
• 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.
• Telephone Single-Channel ECG Transmitter/Receiver System
• Transthoracic Pacemaker Electrode
• Venogram Balloon Catheters

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