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• OmniWire

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  OmniWirePressure guide wire.Find similar products

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.

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Features

Solid proximal core

The solid proximal core is more like a workhorse wire. Embedded conductive ribbons eliminate the need for a hollow hypotube, making a larger solid core possible for torque, push, and kink resistance more like a workhorse wire.

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.

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.

Compatible with iFR and iFR co-registration.

iFR Co-registration makes it easy to identify the precise locations causing ischemia.DocumentationBrochure

•  Product brochure   (2.3 MB) 

Specifications

• 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.
• ©2025 Koniklijke Philips N.V. All rights reserved. Trademarks are the property of Koninklijke Philips N.V. or their respective owners.