Core
This product is no longer available
Core
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.
Choice of FFR, iFR, and IVUS modalities on a single integrated platform
Delivers convenience in your workflow with true integration
Always on and ready for use when you need it
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
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.