June 13, 2024 — The U.S. Food and Drug Administration (FDA) announced that Teleflex, and their subsidiary Arrow ...
June 26, 2023 — The U.S. Food and Drug Administration (FDA) has issued a Class I recall on the Teleflex and Arrow ...
The U.S. Food and Drug Administration (FDA) has issued a Class I recall on the Arrow AutoCAT 2 and AC3 Intra-Aortic ...
September 11, 2012 — Primary results from an ongoing trial by Maquet Cardiovascular using intra-aortic balloon pumps ...
The Arrow AutoCAT 2 WAVE Interaotic balloon pump (IABP) System provides counterpulsation support to the most unstable of ...
April 14, 2009 - The voluntary medical device recall initiated on Feb. 2, 2009 by Arrow International’s Cardiac Care ...
July 25, 2007 - Teleflex Incorporated, a diversified company expanding medical technology business, and Arrow ...
Arrow’s Transradial introducers provide for durable radial artery access while being vessel friendly. Our newest kit ...