Lake Oswego, OR - The first wireless communication system for remote monitoring of implantable pacemakers won FDA approval yesterday. The Biotronik Home Monitoring System allows a Biotronik pacemaker ...

LAKE OSWEGO, Ore.-- (BUSINESS WIRE)--BIOTRONIK, a leading manufacturer of cardiovascular medical devices, announced today that the Food and Drug Administration (FDA) has granted approval for its ...

LAKE OSWEGO, Ore.--(BUSINESS WIRE)--BIOTRONIK, a leading manufacturer of cardiovascular medical devices, announced today that the Food and Drug Administration (FDA) has approved its ProMRI ® Eluna ...

BIOTRONIK ProMRI ® pacing system portfolio gives patients more access to MRI scanning and physicians more options with single and dual chamber pacemaker systems BERLIN & NICE, France--(BUSINESS WIRE)- ...

New pacemakers models Effecta and Estella plus new feature Vp Suppression complete the Evia family LAKE OSWEGO, Ore. & BERLIN--(BUSINESS WIRE)-- BIOTRONIK, a leading manufacturer of implantable ...

BIOTRONIK has announced CE approval of 3 tesla (T) MRI scanning with exclusion zone for its two latest generations of pacemakers. Reportedly, BIOTRONIK is now the only company offering both ...

Biotronik said yesterday it won CE Mark approval in the European Union for 2 next-generation MRI-safe pacemakers. The new devices are compatible with up to 3 tesla MRI scanning machines, the company ...

Biotronik scored FDA approval for its next-generation, MRI-safe pacemaker system, continuing its winning streak for its implantable cardiac devices. The Entovis pacemaker system includes both ...

A federal investigation looking into whether device manufacturer Biotronik used illegal marketing and sales practices to get physicians to use its defibrillators and pacemakers, the New York Times ...

First MR Conditional Pacemaker Portfolio in the US with Single- and Dual-Chamber Pacemakers LAKE OSWEGO, Oregon,—BIOTRONIK, a leading manufacturer of cardiovascular medical devices, announced today ...