Biotronik designed its leadless pacing system to use atrial electrical far-field sensing. The company says it would represent ...
FDA has approved its single- and dual-chamber Entovis pacemakers for use in MRI environments, according to Biotronik Inc. The Lake Oswego, OR-based US subsidiary of Biotronik SE & Co. KG (Berlin) said ...
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 ...
Biotronik is looking to get the FDA's approval for a line of MRI-safe pacemakers--courtesy of Biotronik The FDA approved a clinical trial of Biotronik's proMRI pacemaker, a device designed to operate ...
LAKE OSWEGO, Ore., May 8, 2017 /PRNewswire/ -- BIOTRONIK today announced FDA approval of the company's MultiPole Pacing (MPP) technology, providing physicians with additional treatment options for ...
On November 6, at the International Society for Pharmacoeconomics and Outcomes Research (ISPOR) 14th Annual European Congress in Madrid, Spain, BIOTRONIK presented a series of four posters ...
LAKE OSWEGO, Ore., Aug. 29, 2023 /PRNewswire/ -- BIOTRONIK, a leader in implantable medical device technology, today announced its first US implantation of the new Amvia Edge pacemaker. The procedure ...
Global manufacturer of cardiovascular medical devices BIOTRONIK announced the release of its Renamic product for the Japanese market. The announcement is in response to the dramatic growth of cardiac ...
Materials supplier Syensqo announced today that its Eviva-branded polysulfone (PSU) has been selected by medical device OEM Biotronik for use in the header of its latest Amvia Sky pacemaker models.
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