Core
Precision guided therapy system
This product is no longer available
HCIGTDCOREWorkspaces and systems
  • Standard product photograph
This product is no longer available

Core

Precision guided therapy system
This product is no longer available
HCIGTDCOREWorkspaces and systems
The Core precision guided therapy system allows you to have iFR, FFR and IVUS modalities on a single platform.¹ Core helps provide clarity in your approach and gives you confidence in your decisions.

Specifications
  • Power requirements
    System input
    100, 120V, 220, 240VAC, 50/60Hz, 1000VA
    Monitor
    100V – 240V 50/60Hz, 39W
    Workstation
    100 – 240V, 50/60Hz, 550VA, 825VA
  • Ordering Information
    Core system
    CORE01
    Control pad
    CPADO1
    Bedrail mount
    MNTO1
    Monitor mount
    MNTO2
  • Dimensions
    Workstation
    H=17'', W=10'', D=16.5'' Inches
    Control pad (optional)
    H=2.75'', W=10.5'', D=8.3'' Inches
    Control room controller
    H=5'', W=15'', D=10'' Inches
    Monitor
    H=15''– 19'' (depending upon the stand extension), W=15.8'', D=9.7'' Inches
    Connection box
    H=9.85'', W=2.95'', D=7.75'' Inches

Documentation

Product brochure
PDF|1.48 MB
Disclaimer
1. 505-0100.21, Operator's Manual, Core Integrated, 3.4X (p. 18); 505-0101.16, Operator's Manual, s5 Series FFR_iFR Option, v3.4x (p.15).
2. 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.
3. Patel M. “Cost-effectiveness of instantaneous wave-Free Ratio (iFR) compared with Fractional Flow Reserve (FFR) to guide coronary revascularization decisionmaking.”Late-breaking Clinical Trial
4. 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):1813-18233.
5. VAL RPT, S5-CORE V3.4 SW With CORE Control Pad, 215-0007.02.
6. Product Spec. 809480-001, 202-0407.01
7. Requirements Specification Meridian VH SW, 806000-004 (pg 84).
* Co-registration tools available within IntraSight 7 configuration via SyncVision.
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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