Home
Philips - Click here to navigate to the homepage

Search terms

SyncVision Precision guidance system

SyncVision

Precision guidance system

Find similar products

The SyncVision precision guidance system is suitable with IntraSight and Core Integrated interventional platforms and streamlines lesion assessment, simplifies vessel sizing and enables precise therapy delivery all while integrating seamlessly in daily workflows in interventional suites of choice.

Contact us

Specifications

Power requirements
Power requirements
System input
  • 100V-120V, 50/60Hz, 220-240V, 50/60Hz, 600 VA
Monitor
  • 100-240V, 50/60Hz, 93 VA
Workstation
  • 100-240V, 50/60Hz, 250 VA
Inputs
Inputs
Angiographic system video output
  • Analog or digital
IVUS system
  • CORE system with IVUS version 3.4 and FFR 2.5.1 and IntraSight 5
IVUS catheter
  • Eagle Eye Platinum catheters
Pressure Guidewire
  • Verrata Plus
Dimensions
Dimensions
Workstation
  • Height: 16.5", 39.6 cm; Width: 6.75", 16.2 cm; Depth: 21.25", 51 cm
Bedside joystick
  • Height: 1.5", 3.7 cm; Width: 4.2", 10.7 cm; Depth: 3", 7.6 cm
Monitor
  • Height: 15-19", 41-56 cm; Width: 15.8", 40.2 cm; Depth: 10", 24.7 cm
Ordering Information
Ordering Information
SyncVision precision guidance system
  • Sync002
  • 1. Costa, Angiolillo DJ, Tannenbaum M, et al. Impact of Stent Deployment Procedural Factors on Long-term Effectiveness and Safety of Sirolimus-Eluting Stents (Final results of the Multicenter Prospective STLLR Trial). Am J Cardiol. 2008; 101(12):1704-1711.
  • 2. Renata Rogacka, Azeem Latib, Antonio Colombo. IVUS-Guided Stent Implantation to Improve Outcome: A Promise Waiting to be Fulfilled. Curr Cardiol Rev. 2009;5(2):78–86.
  • 3. Witzenbichler B, Maehara A, Weisz G, et al. Relationship Between Intravascular Ultrasound Guidance and Clinical Outcomes After Drug-Eluting Stents: The ADAPT-DES Study. Circulation. 2014;129:463-470.
  • 4. 202-0013.53 SRS, Sync-Rx System pg 19,24.
  • 5. Jakabcin J1, Spacek R, Bystron M, et al. Long-term health outcome and mortality evaluation after invasive coronary treatment using drug eluting stents with or without the IVUS guidance. Randomized control trial. HOME DES IVUS. Catheter Cardiovasc Interv. 2010;75(4):578-583.
  • 6. 209-0030.02 Test Rpt, Use Validation, SyncVision. Pg. 9, Section 10.3; pg 14 – results.
  • 7. 505-0100.18, Operator’s Manual. (pg 34).
  • 8. 211-0013.31 Test Protocol, Philips Sync-Rx Wizard phase; 211-9913.07 Verification Protocol, Sync-Rx Co-Registration.
  • 9. Patel, et al. ACCF/SCAI/STS/AATS/AHA/ASNC/HFSA/SCCT 2012 Appropriate use criteria for coronary revascularization focused update: a report of the American College of Cardiology Foundation Appropriate Use Criteria Task Force, Society for Cardiovascular Angiography and Interventions, Society of Thoracic Surgeons, American Association for Thoracic Surgery, American Heart Association, American Society of Nuclear Cardiology, and the Society of Cardiovascular Computed Tomography. J Am Coll Cardiol. 2012;59(9):857-881.
  • 10. Kim SH, Kim YH, Kang SJ, et al. Long-term outcomes of intravascular ultrasound-guided stenting in coronary bifurcation lesions. Am J Cardiol. 2010;106(5):612-618.
  • 11. Patel Y, Depta JP, Novak E, et al. Long-term outcomes with use of intravascular ultrasound for the treatment of coronary bifurcation lesions. Am J Cardiol. 2012;109(7):960-965.
  • 12. Davies JE, et al. Coronary artery physiological stenosis mapping: application of pressure wire technology to measure stenosis significance, length, and predict the outcome of intervention. Abstract presented at PCR 2014
  • 13. 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)
  • 14. Fractional Flow Reserve–Guided PCI versus Medical Therapy in Stable Coronary Disease. N Engl J Med. 2012;367(11):991-1001.
  • *Data on file

Media Gallery

Features
Vessel enhancement
Angio+ vessel enhancement

Angio+ vessel enhancement

The SyncVision Angio+ vessel enhancement tool provides clarity in visualizing vessels, which may include tortuous or overlapping vessels and highly stenosed lesions, potentially reducing the number of required views during diagnosis or therapy.
iFR Co-registration
iFR Co-registration

iFR Co-registration

With iFR Co-registration there is no need for hyperemic drugs, no need for time consuming pullback devices and no need for guesswork. Make length measurements without a cumbersome pullback device. Plan your procedure with physiologic guidance.
SyncVision QCA
Quantitative coronary analysis

Quantitative coronary analysis

The SyncVision Angio+ quantitative coronary analysis automatically calculates lumen dimensions and stenosis in real time.
SyncVision IVUS Co-registration localization
SyncVision IVUS Co-registration localization

SyncVision IVUS Co-registration localization

The SyncVision IVUS Co-registration application co-registers the location of the IVUS image on the angiogram and provides easy length and area measurements with a manual IVUS pullback.
IVUS Co-registration: measurement
Simplifies vessel sizing/measurement

Simplifies vessel sizing/measurement

IVUS Co-registration provides easy length measurement with manual IVUS pullback and area/diameter measurements for accurate stent sizing. This feature also provides automated, real-time side-by-side display of co-registered IVUS and angio images to help correlate critical and anatomical landmarks, especially in complex cases, such as bifurcations.⁴, ⁷, ¹⁰, ¹¹
Device positioning
Angio+ device positioning

Angio+ device positioning

The SyncVision Angio+ device positioning tool provides enhanced visualization of device position within the vessel and is designed to help reduce risk of geographic miss, which study data suggests may occur in 66.5% of PCIs.¹
Device motion indication
Healthy-to-healthy landing zones

Healthy-to-healthy landing zones

Intravascular ultrasound guidance helps to confirm healthy-to-healthy landing zones, according to clinical research.³
Device inflation
Angio+ device inflation

Angio+ device inflation

SyncVision Angio+ device inflation provides enhanced visualization of balloon to observe proper inflation. Successful cardiovascular treatment relies on proper balloon inflation, and enhanced imaging can help determine successful inflation functioning.⁸
Device enhancement
Angio+ device enhancement

Angio+ device enhancement

SyncVision Angio+ device enhancement provides enhanced visualization of stent deployment under fluoroscopy to help ensure proper deployment and correct location of deployment.
Addresses imaging challenges
Streamlines and simplifies therapy

Streamlines and simplifies therapy

SyncVision streamlines lesion assessment with co-registration and vessel enhancement, simplifying vessel sizing with real-time QCA and easy length/area/diameter measurement. SyncVision enables precise therapy delivery with Angio+ device detection, offering live stabilization and image enhancement, real-time post-acquisition image processing, and IVUS to assist with confirmation.
IVUS assesses disease
IVUS helps with disease assessment

IVUS helps with disease assessment

IVUS imaging helps physicians assess disease markers, including plaque burden percentage, lesion location and morphology, calcium volume, and the presence of thrombus. It also provides analysis of crucial parameters—like luminal cross-sectional measurements—and helps aid in disease diagnosis.
Fractional Flow Reserve
Fractional Flow Reserve measurement

Fractional Flow Reserve measurement

Various clinical studies demonstrate that physiologic lesion assessment by FFR to guide routine PCI is superior to current angiography guided treatment. This measured ratio represents the potential decrease in coronary flow distal to the coronary stenosis.¹⁴
iFR modality
iFR modality simplifies workflow

iFR modality simplifies workflow

iFR modality simplifies workflow by providing a hyperemia-free measurement to assess lesion significance in as few as five heartbeats. Philips’ proprietary iFR modality has a robust body of clinical evidence with over 9,000 patients in numerous studies and peer-reviewed journal articles.¹³
iFR Scout pullback
iFR Scout pullback

iFR Scout pullback

The iFR Scout pullback shows the most significant gradient in the mid-vessel lesion with diffuse proximal disease.

Specifications

Power requirements
Power requirements
System input
  • 100V-120V, 50/60Hz, 220-240V, 50/60Hz, 600 VA
Monitor
  • 100-240V, 50/60Hz, 93 VA
Workstation
  • 100-240V, 50/60Hz, 250 VA
Inputs
Inputs
Angiographic system video output
  • Analog or digital
IVUS system
  • CORE system with IVUS version 3.4 and FFR 2.5.1 and IntraSight 5
IVUS catheter
  • Eagle Eye Platinum catheters
Pressure Guidewire
  • Verrata Plus
Dimensions
Dimensions
Workstation
  • Height: 16.5", 39.6 cm; Width: 6.75", 16.2 cm; Depth: 21.25", 51 cm
Bedside joystick
  • Height: 1.5", 3.7 cm; Width: 4.2", 10.7 cm; Depth: 3", 7.6 cm
Monitor
  • Height: 15-19", 41-56 cm; Width: 15.8", 40.2 cm; Depth: 10", 24.7 cm
Ordering Information
Ordering Information
SyncVision precision guidance system
  • Sync002

Documentation

Brochure (1)

Brochure

Technical data sheet (1)

Technical data sheet

Related products

*

Contact information

* This field is mandatory
*
*
*
*
*
*
*
*
*
By specifying your reason for contact we will be able to provide you with a better service.
We work with partners and distributors who may contact you about this Philips product on our behalf.
*
*

What does this mean?
Final CEE consent
  • 1. Costa, Angiolillo DJ, Tannenbaum M, et al. Impact of Stent Deployment Procedural Factors on Long-term Effectiveness and Safety of Sirolimus-Eluting Stents (Final results of the Multicenter Prospective STLLR Trial). Am J Cardiol. 2008; 101(12):1704-1711.
  • 2. Renata Rogacka, Azeem Latib, Antonio Colombo. IVUS-Guided Stent Implantation to Improve Outcome: A Promise Waiting to be Fulfilled. Curr Cardiol Rev. 2009;5(2):78–86.
  • 3. Witzenbichler B, Maehara A, Weisz G, et al. Relationship Between Intravascular Ultrasound Guidance and Clinical Outcomes After Drug-Eluting Stents: The ADAPT-DES Study. Circulation. 2014;129:463-470.
  • 4. 202-0013.53 SRS, Sync-Rx System pg 19,24.
  • 5. Jakabcin J1, Spacek R, Bystron M, et al. Long-term health outcome and mortality evaluation after invasive coronary treatment using drug eluting stents with or without the IVUS guidance. Randomized control trial. HOME DES IVUS. Catheter Cardiovasc Interv. 2010;75(4):578-583.
  • 6. 209-0030.02 Test Rpt, Use Validation, SyncVision. Pg. 9, Section 10.3; pg 14 – results.
  • 7. 505-0100.18, Operator’s Manual. (pg 34).
  • 8. 211-0013.31 Test Protocol, Philips Sync-Rx Wizard phase; 211-9913.07 Verification Protocol, Sync-Rx Co-Registration.
  • 9. Patel, et al. ACCF/SCAI/STS/AATS/AHA/ASNC/HFSA/SCCT 2012 Appropriate use criteria for coronary revascularization focused update: a report of the American College of Cardiology Foundation Appropriate Use Criteria Task Force, Society for Cardiovascular Angiography and Interventions, Society of Thoracic Surgeons, American Association for Thoracic Surgery, American Heart Association, American Society of Nuclear Cardiology, and the Society of Cardiovascular Computed Tomography. J Am Coll Cardiol. 2012;59(9):857-881.
  • 10. Kim SH, Kim YH, Kang SJ, et al. Long-term outcomes of intravascular ultrasound-guided stenting in coronary bifurcation lesions. Am J Cardiol. 2010;106(5):612-618.
  • 11. Patel Y, Depta JP, Novak E, et al. Long-term outcomes with use of intravascular ultrasound for the treatment of coronary bifurcation lesions. Am J Cardiol. 2012;109(7):960-965.
  • 12. Davies JE, et al. Coronary artery physiological stenosis mapping: application of pressure wire technology to measure stenosis significance, length, and predict the outcome of intervention. Abstract presented at PCR 2014
  • 13. 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)
  • 14. Fractional Flow Reserve–Guided PCI versus Medical Therapy in Stable Coronary Disease. N Engl J Med. 2012;367(11):991-1001.
  • *Data on file

By clicking on the link, you will be leaving the official Royal Philips Healthcare ("Philips") website. Any links to third-party websites that may appear on this site are provided only for your convenience and in no way represent any affiliation or endorsement of the information provided on those linked websites. Philips makes no representations or warranties of any kind with regard to any third-party websites or the information contained therein.

I understand