Benzinga | Oct 1, 2020 06:41AM EDT

Teleflex Announces The Expanded Indications For The Arrow EZ-IO Intraosseous Vascular Access System

WAYNE, Pa., Oct. 01, 2020 (GLOBE NEWSWIRE) -- Teleflex Incorporated (NYSE:TFX), a leading global provider of medical devices for critical care and surgery, has announced it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to expand the Indications for Use of the Arrow(r) EZ-IO(r) Intraosseous Vascular Access System. This device can be used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases.



The Arrow(r) EZ-IO(r) System is now available with the expanded indication stating use of the device may be extended for up to 48 hours when alternate intravenous access is not available or reliably established in adults, and in pediatric patients 12 years and older.

"Vascular access is one of the most basic, yet critical, components of patient care," said Michelle Fox, Corporate Vice President and Chief Medical Officer, Teleflex. "The ability to use the EZ-IO(r) System for a longer dwell time provides clinicians the option to utilize intraosseous (IO) access for the entire duration of therapy in patients with difficult vascular access where therapy is required for up to 48 hours."

In patients who require longer-term access, the expanded indication gives clinicians additional time to establish vascular access safely, choosing the appropriate device and optimal site of insertion to meet the patient's clinical needs. "These benefits are of particular importance in a time of constrained resources and patient surge," said Ms. Fox.

Expanded Indications for Use of the Arrow(r) EZ-IO(r) System are now as follows:

For intraosseous access anytime in which vascular access is difficult to obtain in emergent, urgent or medically necessary cases for up to 24 hours.

Adults Pediatrics (?21 years old) * Proximal humerus * Distal femur * Proximal tibia * Proximal humerus * Distal tibia * Proximal tibia * Distal tibia

Use of the device may be extended for up to 48 hours when alternate intravenous access is not available or reliably established.

Adults Pediatrics (?12 years through 21 years old): * Proximal humerus * Distal femur * Proximal tibia * Proximal humerus * Distal tibia * Proximal tibia * Distal tibia

"We pursued this indication expansion with the FDA based on input from clinicians, who were seeking a longer dwell time," said Kevin Robinson, Vice President and General Manager, Anesthesia and Emergency Medicine Division, Teleflex. "We are pleased to make this announcement now, allowing clinicians expanded options for managing patients with difficult vascular access."