OmniWire
Pressure guide wire.
  • OmniWire shape retention and recovery
  • OmniWire specifications and measurements.
  • OmniWire preparation
  • OmniWire measures FFR and iFR, the only hyperemia-free index validated in the largest physiology clinical outcomes studies with data from more than 4,500 patients. Only offered by Philips, iFR is an evidence-based methodology that improves outcomes, saves time, and reduces patient discomfort.¹,²
  • Introducing Philips OmniWire pressure guide wire
  • New design from tip to tail to improve navigation in complex anatomy.
  • OmniWire shape retention and recovery
  • Until now, all pressure wires used a hollow hypotube to house electrical leads or optical fibers that carry the pressure signals. OmniWire uses a solid construction with conductive ribbons embedded in its outer layer. This innovation makes a larger solid core possible, similar to the design of your workhorse wire, providing the handling and durability needed for complex and multi-vessel cases.
  • Standard Product Photograph

OmniWire

Pressure guide wire.
OmniWire combines a unique solid core workhorse design with iFR proven outcomes and iFR Co-registration compatibility, making it easy to use physiology throughout complex cases. ¹,²,³ • New Nitinol distal core increases durability and shape recovery. • Unique solid core improves torque and pushability. • Integrated conductive bands for greater signal reliability.

Features
Only iFR has co-registration for advanced physiologic guidance.
Map iFR values directly onto the angiogram, so you can see precisely which parts of a vessel are causing ischemia.
iFR has co-registration
Compatible with iFR and iFR co-registration.
iFR Co-registration makes it easy to identify the precise locations causing ischemia.
Compatible with iFR and iFR co
Nitinol distal core and integrated conductive bands.
The Nitinol core is super elastic for durability and shape recovery. Useful for long multi-vessel procedures. Integrated conductive bands enable the back end to be a continuous piece with no joints, designed to reduce kinking, facilitate device loading, device delivery, and easy reconnects.
Nitinol distal core


Specifications
  • Straight tip
    89185
    Size 185 CM
  • J-tip
    89185J
    Size 185 CM

Documentation

Product brochure
PDF|2.30 MB
Disclaimer
1. Davies JE, et al., Use of the Instantaneous Wave-free Ratio or Fractional Flow Reserve in PCI. N Engl J Med. 2017 May 11;376(19):1824-1834.
2. Gotberg M, et al., iFR-SWEDEHEART Investigators. Instantaneous Wave-free Ratio versus Fractional Flow Reserve to Guide PCI. N Engl J Med. 2017 May 11;376(19):1813-1823.
3. Comparisons to Verrata Plus. Data/report internally on file or internal company’s data on file. Verification Report, D000410086/A.
4. Data on file.
5. Patel M. “Cost-effectiveness of instantaneous wave-Free Ratio (iFR) compared with Fractional Flow Reserve (FFR) to guide coronary revascularization decision-making.” Late-breaking Clinical Trial presentation at ACC on March 10, 2018.
Product availability is subject to country regulatory clearance. Please contact your local sales representative to check the availability in your country.
Always read the label and follow the directions for use.
Philips medical devices should only be used by physicians and teams trained in interventional techniques, including training in the use of this device.
Philips reserves the right to change product specifications without prior notification.
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