GlobeNewswire10.01.20
Teleflex Incorporated, a 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 EZ-IO 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 EZ-IO 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 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 Fox.
Expanded Indications for Use of the Arrow EZ-IO 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.
Use of the device may be extended for up to 48 hours when alternate intravenous access is not available or reliably established.
“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.”
The Arrow EZ-IO 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 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 Fox.
Expanded Indications for Use of the Arrow EZ-IO 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) |
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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) |
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“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.”