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 systems offer the choice of imaging and physiology on a single integrated platform.¹ Core helps provide clarity in your approach, confidence in your decisions, and convenience in your diagnostic and interventional workflows.

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. VAL RPT, S5-Core V3.4 SW with Core Control Pad, 215-0007.02.
3. Product Spec. 809480-001, 202-0407.01.
4. Requirements Specification Meridian VH SW, 806000-004 (pg 84).
5. An iFR cut-point of 0.89 matches best with an FFR ischemic cut-point of 0.80 with a specificity of 87.8% and sensitivity of 73.0%. (iFR Operator’s Manual 505-0101.23)
6. N Engl J Med. 2012;367(11):991-1001.
7. Witzenbichler B et al. Relationship Between Intravascular Ultrasound Guidance and Clinical Outcomes After Drug-Eluting Stents: The ADAPT-DES Study. Circulation 2014 Jan: 129,4;463-470
8. Ahn et al. Meta-Analysis of Outcomes After Intravascular Ultrasound Guided Versus Angiography-Guided Drug-Eluting Stent Implantation in 26,503 Patients Enrolled in Three Randomized Trials and 14 Observational Studies. Am J Cardiol 2014; 113:1338-1347
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.