Biotronik Ag

Contact: Markus Angst
Address: Ackerstrasse 6, Bulach CH-8180, Switzerland
Phone: +41-(44)-864-5111 | Map/Directions >>

Profile: Biotronik Ag offers guidewires, percutaneous catheters, percutaneous catheterization vessel dilators and peripheral transluminal angioplasty catheters.

FDA Registration Number: 8043892
US Agent: Jon Brumbaugh / Biotronik, Inc.
Phone: +1-(888)-345-0374 Fax: +1-(503)-635-9936 E-Mail:

9 Products/Services (Click for related suppliers)

• Drug-Eluting Permanent Defibrillator Electrodes (FDA Code: NVY)

• 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 Permanent Pulse Generator (FDA Code: NVZ)

• 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.

• 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.

• 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.