Business Wire

Teleflex to Introduce the New TrapLiner® Catheter in Europe and Showcase the Arrow® AC3 Optimus™ Intra-Aortic Balloon Pump (IABP) at the European Association for ...

WAYNE, Pa.--(BUSINESS WIRE)--Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies for critical care, urology and surgery, coronary and peripheral interventions, will ...
Fierce Healthcare

Teleflex Signs New Agreement with HealthTrust for Arrow Intra-Aortic Balloon Pumps and Catheters

LIMERICK, Pa.--(BUSINESS WIRE)-- Teleflex Incorporated (NYSE:TFX), a leading global provider of medical devices for critical care and surgery, has announced a new agreement with HealthTrust Purchasing ...
Medscape

FDA Expands List of Getinge IABP System and Component Shortages

The US Food and Drug Administration (FDA) today issued a letter to healthcare providers describing a current shortage of Getinge intra-aortic balloon pump (IABP) catheters and other components.
Business Insider

Teleflex Gets FDA 510(k) Clearance For Arrow AC3 Optimus IABP

(RTTNews) - Teleflex Inc. (TFX), a provider of medical technologies for critical care and surgery, announced 510(k) clearance from the U.S. Food and Drug Administration for its AC3 Optimus ...
MD&M East

Teleflex Arrow FiberOptix and UltraFlex (IAB) Catheter Kits Recall Identified as FDA Class I

Teleflex and its subsidiary Arrow International recently received FDA Class I designation for its recall of the Arrow FiberOptix and UltraFlex Intra-Aortic Balloon (IAB) catheter kits after reporting ...
Medscape

FDA Issues Recall for Arrow International IAB Catheters

April 16, 2009 (Rockville, Maryland) — The FDA has issued a class 1 recall for a number of intra-aortic balloon pump (IAB) catheters manufactured by Teleflex's Arrow International because of a fault ...