After nearly a decade of research and development, Biotronik, Berlin, Germany, has released the Plexa ProMRI, the smallest (7.8F) MR-conditional tachycardia lead available in the United States. The FDA recently approved Plexa ProMRI for use with implantable cardioverter defibrillators (ICDs) and heart failure devices.
The lead’s performance-driven, high-voltage wire design maximizes durability by extending to the area between the distal and proximal shock coil, with negligible impact on electrical impedance. The lead’s design offers physicians uniform handling during placement and the modified screw performs more reliably in their hands.
“This is another advancement in efforts to further improve the performance and maneuverability of ICD leads,” says Theofanie Mela, MD, an electrophysiologist at Massachusetts General Hospital and one of the first physicians in the US to implant Plexa. “Patients who require ICDs are understandably concerned about reliability, and that underscores the need for durable ICD leads to choose from.”
Plexa ProMRI’s suite of tactile design elements provides physicians with an advanced, high-performing, MR-conditional ICD lead for tachycardia patients with various patient anatomies. Plexa ProMRI leads are available in various DF4, DF-1 and DX configurations.
“Biotronik is committed to continuously advancing the quality of our cardiovascular solutions for patients and physicians because excellence never rests,” says Marlou Janssen, president of Biotronik Inc. “With a commitment to clinicial research, we have championed reliable leads for more than 50 years. Biotronik invested nearly a decade of research and development to bring Plexa ProMRI to market, and we’ll continue these efforts to ensure Plexa ProMRI consistenly surpasses expectations.”
For more information, visit Biotronik.