Teleflex Expands Intraosseous Vascular Access Portfolio with New Arrow™ EZ-IO™ Intraosseous Access Procedure Tray
09 Mai 2024 - 12:30PM
Teleflex Incorporated (NYSE: TFX), a global leader in medical
technologies and pioneer in intraosseous vascular access, today
announced the launch of the Arrow™ EZ-IO™ Intraosseous Access
Procedure Tray. This sterile, single-use tray includes all the
components required for the IO access procedure, enabling a
streamlined clinician workflow.
The new Arrow™ EZ-IO™ Procedure Tray includes the
first FDA-cleared sterile, single-use, battery-powered driver,
providing clinicians with an IO access option that can be used in a
sterile field in the operation room and any other area of the
hospital that requires a sterile field. The tray is packaged with
an Arrow™ EZ-IO™ Intraosseous Needle Set (15mm, 25mm, or 45mm),
which is designed to help ensure a fast,1 precise, and steady
insertion. Additional components include:
- Pre-filled saline syringe and ChloraPrep™ Frepp™ Clear
applicator
- EZ-Stabilizer™ Dressing
- EZ-Connect™ Extension Set
- SharpsAway™ II Locking Sharps Disposal Cup
- EZ-IO™ Patient Wristband
- Quick Reference Guide, printed on underside of every tray
lidstock
“The Arrow™ EZ-IO™ Procedure Tray was developed after research
was conducted with healthcare professionals who may benefit from an
intraosseous access solution in a complete, convenient and sterile
kit,” stated Michelle Fox, Corporate Vice President and Chief
Medical Officer at Teleflex. “This addition to our IO access
portfolio reflects our relentless pursuit of innovation to empower
clinicians and elevate patient care in challenging vascular access
situations.”
Delayed vascular access can result in treatment delays, which
can lead to adverse outcomes.2-5 The Arrow™ EZ-IO™ Intraosseous
Access System can be used when intravenous access is difficult or
impossible to obtain in emergent, urgent, or medically necessary
cases. In a recent survey of hospital-based clinicians, 65%
recalled situations where their IO device was not accessible during
a time-critical difficult vascular access situation.6 More than 75%
of clinicians surveyed agree that a single-use tray would increase
the accessibility and convenience of IO access devices.6 The new
Arrow™ EZ-IO™ Procedure Tray was designed for compact storage on
hospital shelving and is small enough to fit in any code cart.
Clinicians now have a choice between the reusable Arrow™ EZ-IO™
Power Driver and the new single-use tray. “The new Arrow™ EZ-IO™
Procedure Tray was designed to optimize efficiency in gaining fast
vascular access while increasing the accessibility of the EZ-IO™
System,” said Kevin Robinson, President and General Manager of
Anesthesia and Emergency Medicine, Teleflex. “We listened to the
challenges healthcare professionals face daily and are proud to
introduce a solution that combines our industry-backed IO access
device with enhanced convenience.”
About Teleflex IncorporatedAs a global provider
of medical technologies, Teleflex is driven by our purpose to
improve the health and quality of people’s lives. Through our
vision to become the most trusted partner in healthcare, we offer a
diverse portfolio with solutions in the therapy areas of
anesthesia, emergency medicine, interventional cardiology and
radiology, surgical, vascular access, and urology. We believe that
the potential of great people, purpose driven innovation, and
world-class products can shape the future direction of
healthcare.
Teleflex is the home of Arrow™, Barrigel™, Deknatel™, QuikClot™,
LMA™, Pilling™, Rüsch™, UroLift™ and Weck™ – trusted brands united
by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For
more information, please visit teleflex.com.
Forward-Looking StatementsAny statements
contained in this press release that do not describe historical
facts may constitute forward-looking statements. Any
forward-looking statements contained herein are based on our
management's current beliefs and expectations, but are subject to a
number of risks, uncertainties, and changes in circumstances, which
may cause actual results or company actions to differ materially
from what is expressed or implied by these statements. These risks
and uncertainties are identified and described in more detail in
our filings with the Securities and Exchange Commission, including
our Annual Report on Form 10-K.
Chloraprep and Frepp are trademarks of Carefusion or one of its
subsidiaries. Teleflex, the Teleflex logo, Arrow, EZ-IO,
EZ-Connect, EZ-Stabilizer, Deknatel, LMA, Pilling, QuikClot, Rüsch,
SharpsAway, UroLift and Weck are trademarks or registered
trademarks of Teleflex Incorporated or its affiliates, in the U.S.
and/or other countries.© 2024 Teleflex Incorporated. All rights
reserved. MC-009356
References:
- Davidoff J, Fowler R, Gordon D, et al. JEMS.
2005;30(10):s20-s23. Research sponsored by Teleflex
Incorporated
- Donnino MW, Salciccioli JD, Howell MD, et al. BMJ.
2014;348:g3028.
- Gayet-Ageron A, Prieto-Merino D, Ker K, et al. Lancet.
2018;391(10116):125-132.
- Ferrer R, Martin-Loeches I, Phillips G, et al. Crit Care Med.
2014;42(8):1749-1755.
- Fonarow GC, Smith EE, Saver JL, et al.
Circulation.2011;123(7):750-758
- Double-blinded online survey of n=209 respondents—including 159
target hospital-based clinicians in the Emergency Department,
Trauma Unit, Intensive Care Unit/Critical Care Unit, or on the
Rapid Response or Code Team—conducted 11-OCT-2022 to 21-OCT-2022.
Teleflex data on file. D044709.
The Arrow™ EZ-IO™ Single-Use IO Tray is indicated for
intraosseous access anytime in which vascular access is difficult
to obtain in emergent, urgent or medically necessary cases for up
to 24 hours. For patients ≥ 12 years old, the device may be
extended for up to 48 hours when alternate intravenous access is
not available or reliably established.
Rx Only. CAUTION: Federal (USA) law restricts this device to
sale by or on the order of a physician.The Arrow™ EZ-IO™ Needle Set
is Sterile, Single Use: Do not reuse, reprocess or re-sterilize.
Reuse of device creates a potential risk of serious injury and/or
infection which may lead to death. Refer to Instructions for Use
for complete warnings, indications, contraindications, precautions,
and potential complications.
Contact:Teleflex Incorporated:Lawrence
KeuschVice President, Investor Relations and Strategy
Developmentinvestors.teleflex.com610-948-2836
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