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EV HEMOSTASIS INTRODUCER

  • Sheath Length (cm) 12
  • Guidewire Diameter (in) 0.035
  • French Size 4
Designed as a standard introducer for both diagnostic and interventional catheterizations
Co-extruded proprietary materials, combined with the smooth transitions and kink resistance improve insertion characteristics and is designed to reduce vessel trauma
Shorter and stronger dilator for optimal insertion performance
Hemostasis valve seals around smaller diameter guidewires (4 F 9 F Models)
Convenient suture ring location
Snap lock feature secures dilator in sheath during insertion
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Service Kit

Service Kit for Wi-Box unit, RadiAnalyzer Xpress and QUANTIEN systems
AO and PW pressure test probes
Electrical safety test adapters
Enables functional testing and electrical safety measurement
2 screws to access the metal parts (on the DVI-port)
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SHEATH OBTURATOR

  • French Size 4
  • Obturator Length (cm) 15
Designed to interlock with hemostasis introducers to maintain sheath patency and general management of the introduction site
Use an obturator at least one french size smaller than the sheath to facilitate blood pressure monitoring through the sidearm and to accommodate heparin circulationFrench Size
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INTEGRATED FFR PLATFORM

Integrated platform for fast, easy FFR procedures
Wireless patient environment
Permanent cath lab integration or mobile
Touch screen andor remote control user interaction
Compatible with Wi-Box unit, PressureWire Aeris and PressureWire Certus guidewires
Flexible mounting solutions: Desktop Stand, Wall Mount, Pole Bracket (VESA 75x75 or 100x100 compatible)
Ethernet network connectivity (RJ45, 100Mbit)
Video Out for cath lab screen display DVI-I, both analog and digital
DICOM Worklist management
Export to DICOM, Network and USB as Spreadsheet file, Picture or RadiView viewable format.
Optional analog AOECG from recording system
Optional analog AUX output ports
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SYSTEM SETUP

rief Summary: Please review the Instructions for Use prior to using these devices for a complete listing of indications, contraindications, warnings, precautions, potential adverse events and directions for use.

QUANTIEN system is designed, developed and manufactured by St. Jude Medical Systems AB. Product referenced is approved for CE Mark. ILUMIEN and ILUMIEN OPTIS systems and OPTIS integrated system are designed, developed and manufactured by LightLab Imaging, Inc.
Unless otherwise noted, indicates that the name is a trademark of, or licensed to, St. Jude Medical or one of its subsidiaries. ST. JUDE MEDICAL and the nine-squares symbol are trademarks and service marks of St. Jude Medical, Inc. and its related companies.
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XPRESS MEASUREMENT

Used together with the PressureWire Certus guidewire for real-time measurement of pressure (FFR), flow (CFR), index of microcirculatory resistance (IMR) and intravascular temperature
Connects with any cath lab system
Lightweight and compact monitor size allows bedside mounting for convenient access to key information
High-speed connectivity to PC
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Remote

Brief Summary: Please review the Instructions for Use prior to using these devices for a complete listing of indications, contraindications, warnings, precautions, potential adverse events and directions for use.

QUANTIEN system is designed, developed and manufactured by St. Jude Medical Systems AB. Product referenced is approved for CE Mark.
Unless otherwise noted, indicates that the name is a trademark of, or licensed to, St. Jude Medical or one of its subsidiaries. ST. JUDE MEDICAL and the nine-squares symbol are trademarks and service marks of St. Jude Medical, Inc. and its related companies.
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RIGID SADDLE RING

  • Ring Size nternal 2-D Orifice Area (mm2)
  • 24 227
duct Highlights
Designed to restore the shape of a healthy mitral annulus1
Titanium core maintains the anatomical shape and provides annular remodeling
Saddle shape contributes to efficient distribution of leaflet stress and chordal tension, which may increase repair durability1-4
EZ Suture cuff is supported by a unique triangular core for a larger suture targetRing Size
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TRANSDUCER CABLE

  • Length (m) 2
Transducer adapter cable intended for connection of RadiAnalyzer Xpress to NAMIC AO transducer and hemodynamic recording systemNAMIC is a registered trademark of Navilyst Medical, Inc. RadiAnalyzer is designed, developed and manufactured by St. Jude Medical Systems AB.
Please review the Instructions for Use prior to using these devices for a complete listing of indications, contraindications, warnings, precautions, potential adverse events and directions for use.
Product referenced is approved for CE Mark.
Unless otherwise noted, indicates that the name is a trademark of, or licensed to, St. Jude Medical or one of its subsidiaries. ST. JUDE MEDICAL and the nine-squares symbol are trademarks and service marks of St. Jude Medical, Inc. and its related companies.
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Wireless Solution

  • Series WI-BOX
Wi-Box unit connects to RadiAnalyzerRadiAnalyzer Xpress system with one cable or to the QUANTIEN, ILUMIEN or ILUMIEN OPTIS systems directly via radio
Permanently mounted under the cath lab table, one Wi-Box unit per room
AO pressure is routed through the Wi-Box unit to the cath labs hemodynamic recording system
Enables a mixed environment with all St. Jude Medical FFROCT platforms
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XPRESS OPTICAL CABLES

  • Length (m) 10
Brief Summary: Please review the Instructions for Use prior to using these devices for a complete listing of indications, contraindications, warnings, precautions, potential adverse events and directions for use.

RadiAnalyzer, RadiView and PhysioMon systems are designed, developed and manufactured by St. Jude Medical Systems AB. Product referenced is approved for CE Mark.
Unless otherwise noted, indicates that the name is a trademark of, or licensed to, St. Jude Medical or one of its subsidiaries. ST. JUDE MEDICAL and the nine-squares symbol are trademarks and service marks of St. Jude Medical, Inc. and its related companies.
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Optical Modem

Connects RadiAnalyzer and RadiAnalyzer Xpress systems to PC via USB
Compatible with RadiAnalyzer and RadiAnalyzer Xpress systemsBrief Summary: Please review the Instructions for Use prior to using these devices for a complete listing of indications, contraindications, warnings, precautions, potential adverse events and directions for use.

RadiAnalyzer system is designed, developed and manufactured by St. Jude Medical Systems AB. Product referenced is approved for CE Mark.
Unless otherwise noted, indicates that the name is a trademark of, or licensed to, St. Jude Medical or one of its subsidiaries. ST. JUDE MEDICAL and the nine-squares symbol are trademarks and service marks of St. Jude Medical, Inc. and its related companies.
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TIP UNIVERSAL TEMPERATURE

  • Usable Length (cm) 115
  • Electrode Spacing (mm) 1
Automatic steering lock reduces catheter manipulation
Bi-directional tip deflection
Thermocouple and Thermistor temperature monitoring capability
ComfortGrip ergonomic handleBrief Summary: Please review the Instructions for Use prior to using these devices for a complete listing of indications, contraindications, warnings, precautions, potential adverse events and directions for use.

Unless otherwise noted, indicates that the name is a trademark of, or licensed to, St. Jude Medical or one of its subsidiaries. ST. JUDE MEDICAL and the nine-squares symbol are trademarks and service marks of St. Jude Medical, Inc. and its related companies.

2017 St. Jude Medical, Inc. All rights reserved.Usable Length (cm)
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SENSOR ENABLED

  • Length (cm) 115
Fully integrated with the EnSite Precision Cardiac Mapping System and MediGuide Technology
Gain additional reach by using a bi-directional handle with both symmetric and asymmetric curves, or select a unidirectional option
Fast, easy setup and enhanced workflow is obtained through an intuitive display of CF data
CF parameters:
- FTI Force Time Integral parameter measured in real-time during catheter ablation procedures
- LSI Leision Index combining contact force, radiofrequency (RF) application duration, and RF current
Fiber optic contact force technology that provides superior accuracy and reliable readings
Requires TactiSys Quartz equipment and EnSite Contact Force Module software
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QUARTZ EQUIPMENT

Fully integrated display with the EnSite Precision Cardiac Mapping System and Contact Force Module
Optical white light interferometry sensor based technology for enhanced resolution and measurement stability
Fast sampling rate for accurate contact force information
No lengthy startup calibration procedure required
Proprietary indices of Force Time Integral (FTI) and Lesion Index (LSI) designed to assess lesion quality
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BRAIDED TRANSSEPTAL GUIDING INTRODUCERS SL SERIES

  • Length 63 cm
  • Sheath Usable Length (cm) 63
  • Dilator Usable Length (cm 63
Braided sheath facilitates torqueability, pushability and catheter stability
Ultra-soft tip for atraumatic performance
Multiple curve options available
Smaller offset sideholes reduce likelihood of guidewire exiting sidehole
Ultimum valve for effective hemostasis and minimal risk of air inspiration
Accommodates a 71 cm BRK Transseptal Needle (Reorder Number 407200 or 407201)
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QUADRA ASSURA

The Quadra Assura MP CRT-D brings MultiPoint pacing, an exclusive St. Jude Medical technology, to cardiac resynchronization therapy defibrillators (CRT-Ds). The Quadra Assura MP CRT-D and Quartet quadripolar LV pacing lead feature four pacing electrodes and 10 pacing vectors, providing more options and greater control to minimize implant complications such as diaphragmatic stimulation and high pacing threshold.
Quadra Assura MP CRT-D is an MRI Ready device when used in combination with MR Conditional leads. This device has been tested for safe performance of an MRI scan using a 1, 5 T (Tesla) field-strength MRI scanner.a, b The recent IDE study4 post-hoc subanalysis (n = 199) showed that wider cathode spacing and near-simultaneous intraventricular timing delays provide best MPP technology response at 87 percent and super-response at 54 percent (52 patients).4
See details of the U.S. IDE study and other clinical support for MultiPoint pacing.
MULTIPOINT PACING HAS ALSO DEMONSTRATED:
90% response rate with MultiPoint pacing at 12 months measured by ESV decrease > 15%5
95% response rate with MultiPoint pacing at 12 months measured by 1 decrease in NYHA class5
90% response rate with MultiPoint pacing at 12 months measured by Packers score5
19% absolute improvement in patients for CRT response at 12 months when compared to traditional biventricular (BiV) pacing with a quadripolar lead6
44% relative reduction in nonresponders at 12 months when compared to traditional BiV pacing with a quadripolar lead6The recent IDE study4 post-hoc subanalysis (n = 199) showed that wider cathode spacing and near-simultaneous intraventricular timing delays provide best MPP technology response at 87 percent and super-response at 54 percent (52 patients).4
See details of the U.S. IDE study and other clinical support for MultiPoint pacing.
MULTIPOINT PACING HAS ALSO DEMONSTRATED:
90% response rate with MultiPoint pacing at 12 months measured by ESV decrease > 15%5
95% response rate with MultiPoint pacing at 12 months measured by 1 decrease in NYHA class5
90% response rate with MultiPoint pacing at 12 months measured by Packers score5
19% absolute improvement in patients for CRT response at 12 months when compared to traditional biventricular (BiV) pacing with a quadripolar lead6
44% relative reduction in nonresponders at 12 months when compared to traditional BiV pacing with a quadripolar lead6
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LEFT ATRIAL APPENDAGE

Designed to completely seal the widest range of LAA anatomy
Flexible Nitinol braid allows the device to conform to different types of LAA anatomy.
Available in the most complete range of sizes to seal LAAs with landing zones from 11 to 31 mm in diameter.1
Proximal device positioning allows for placement regardless of distal anatomy or existence of multiple distal lobes.1
Controlled device positioning with minimal steps
Preloaded to streamline preparation.
Single piece cable designed for ease of device delivery and better control during deployment.
Longer waist allows for more flexible placement within the LAA.
Can be fully repositioned and recaptured for optimal placement.
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AMPLATZER

This device is commercially available for use in select international markets.
Designed for Complete Occlusion of the LAA
Atrial fibrillation is the biggest risk factor for ischaemic stroke. It has a crippling effect on patients lives and is one of the top health care costs in many countries.2-5 Current evidence suggests that percutaneous occlusion of the left atrial appendage (LAA) reduces the risk of thromboembolic complications associated with nonvalvular atrial fibrillation.1
We designed the AMPLATZER Cardiac Plug (ACP) to provide complete occlusion of the LAA at the orifice. Made of a flexible braided Nitinol mesh, the ACP allows for controlled, precise deployment and conformability to different appendage anatomies.
Designed for LAA closure
Lobe conforms to the inner wall of the LAA and requires only a minimum depth of 10 mm for deployment, providing secure placement in a shallow landing zone.
Self-orienting disc is designed to completely cover the orifice of the LAA.
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FAMILY OF VASCULAR PLUGS

Advancing the Standard of Care in Peripheral Embolization
Vascular plugs are a more advanced alternative for peripheral embolization. A single device from the AMPLATZER Family of Vascular Plugs embolizes a vessel that would often require many coils, which makes it an efficient and cost-effective1-2 alternative. A vascular plug can also be easily repositioned and redeployed during a procedure for greater precision.
Advantages of single device occlusion
We have designed our AMPLATZER Family of Vascular Plugs to provide optimal embolization through single device occlusion, with full cross-sectional vessel coverage and precise, controlled deployment.
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MUSCULAR VSD OCCLUDER

The Innovative Answer to Muscular VSD Closure
Ventricular septal defects (VSDs) are the most commonly found congenital heart defect.1 The AMPLATZER Muscular VSD Occluder was specially designed to close complex muscular VSDs, including in patients considered to be high risk for standard surgical repair.
Engineered for complete closure
Device waist centers and fills the defect.
Polyester material promotes occlusion and tissue in-growth.
7 mm waist length accommodates the thickness of the muscular ventricular septal wall.
Procedural flexibility
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PFO OCCLUDER

Simple and Confident Transcatheter PFO Closure
The AMPLATZER PFO Occluder is a double-disc device comprised of Nitinol mesh and polyester fabric. It has been designed to close all types of patent foramen ovale (PFO) with an easy-to-perform deployment procedure.
Excellent clinical results
High closure rates, with 94% of patients showing effective closure (0 9 microbubbles at both rest and Valsalva) at 6 months1
Extensive clinical experience with over 60, 000 devices implanted worldwide2
Nitinol and polyester construction promotes endothelialization
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SEPTAL OCCLUDER

Simplicity Matters
Minimally invasive transcatheter closure is the primary treatment option for secundum atrial septal defects (ASD).1 The AMPLATZER Septal Occluder is the proven standard of care in transcatheter ASD closure.1, 2 It is designed to appose the septal wall on each side of the defect and create a platform for tissue in-growth after implantation.
Designed for ASD closure
Shape-memory Nitinol mesh securely apposes both sides of the septal wall.
A wide waist centers the device and fills the ASD.
Polyester material promotes occlusion and tissue in-growth.
Device can be recaptured and redeployed for precise placement.
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NEUROSTIMULATOR SYSTEM

RG stimulation: A clinically proven therapy
DRG stimulations effectiveness has been proven in many international studies along with the U.S. ACCURATE study, the largest randomized neurostimulation clinical trial that compares conventional tonic SCS with DRG stimulation to treat chronic intractable CRPS of the lower limbs and peripheral causalgia. The findings demonstrate DRG stimulation enhances your ability to:
Deliver superior pain relief:* The ACCURATE study showed that DRG stimulation is clinically superior to conventional tonic SCS in treating lower extremity pain (i.e., foot, knee, hip and groin) associated with focal chronic intractable pain. The stimulation of the DRG allows for the ability to precisely stimulate specific regions of the dermatome that is otherwise difficult to individually target with broadly applied traditional SCS.
Treat more patients: DRG stimulation provides a therapy option for patients with focal chronic intractable pain conditions such as CRPS of the hand and foot, groin pain, peripheral neuropathic and phantom limb pain.2
Provide stable pain relief: Studies have shown that DRG stimulation provides stable, long-term pain relief for at least 12 months.4
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BRIO RECHARGEABLE IPG

Simple and reliable charging
The Brio IPG is tested and approved for at least 10 years of sustained therapy, even when used at high power settings, with no manufacturer-imposed shut-off date.1
Other benefits include:
Advanced antenna technology enables easy, reliable and fast recharging
Flexible recharging schedule helps ensure patients comply with their therapy
Large coupling target makes it easy to establish and maintain optimal coupling at depths of up to 2.25 cm
More flexibility during implant
Surgeons have multiple implant options:
At 18 cc, the Brio IPG is the smallest rechargeable deep brain stimulation IPG1, 2
Its small size and thin 10 mm profile allow flexibility in implant location, accommodating a broader range of patients
Advanced antenna technology allows the Brio IPG to be implanted at a depth of up to 2.25 cm, offering the potential for increased patient comfort and placement options
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ACUTE CIRCULATORY SUPPORT SYSTEM

ee more details about Full MagLev flow technology.
Addressing the broadest spectrum of clinical challenges
The system helps you provide optimal patient care for every application5: biventricular assist device (BiVad), left ventricular assist device (LVAD), right ventricular assist device (RVAD), extracorporeal membrane oxygenation (ECMO)extracorporeal life support (ECLS), weanbridge to recovery, bridge to decision, bridge to durable ventricular assist device (VAD), bridge to transplantation.
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DEFIBRILLATION LEAD

MRI Ready lead models
The Durata defibrillation lead allows patients to safely undergo an MRI scan* when used in combination with a St. Jude Medical MRI Ready device.1, 2
Lead reliability with Optim lead insulation
The Durata defibrillation lead has a proven structural design. It uses Optim lead insulationa unique material, with excellent long-term durability3and thin, 7 F sizing, which better accommodates multiple leads in a single vessel. It is designed to deal with challenging ICD lead cases, including cases requiring multilead systems, lead replacement or with patients who have small or tortuous veins.
Long-term performance
Durata defibrillation leads use St. Jude Medical exclusive Optim lead insulation, a unique hybrid of silicone and polyurethane, designed to:
Minimize lead abrasion
Increase flexibility and lubricity4
Provide lead-on-lead and lead-on-can abrasion resistance in multi-lead systems
Restrict tissue growth into shock coils, by utilizing flat-wire coils with silicone backfill
Research has shown that the Durata defibrillation lead has experienced:
99.6% abrasion-free rate based on 8 years of data5
85% reduction in abrasion rates vs. St. Jude Medical silicone leads5
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MULTI-ELECTRODE RENAL DENERVATION SYSTEM

Cutting-Edge Technology for Renal Denervation
Renal denervation has been shown to effectively reduce systolic blood pressure.1 The next generation EnligHTN renal denervation system improves on existing technology to reduce the number of catheter manipulations needed to disrupt the sympathetic nerve network.
The EnligHTN renal denervation system delivers a repeatable ablation pattern using four evenly spaced electrodes. Fast, intuitive and predictable, the non-occluding multi-electrode ablation catheter offers cutting-edge efficiencies that enable unparalleled speed and placement accuracy in renal denervation.1, 2
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CARDIAC MAPPING SYSTEM

Transform procedures with intuitive automation1, 2
Advanced mapping is complex. You need precise information quickly to make sound decisions. The EnSite Precision cardiac mapping system helps you decrease mapping time using intelligent automation tools.*1, 2 The system:
Works with the EnSite AutoMap module, so you can enhance VT mapping with automated, advanced morphology matching capability1, 2
Lets you automatically reject catheter ectopy
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MITRAL STENTED TISSUE VALVE

Redefining Performance
The Epic Mitral stented tissue valve with Linx AC technology offers the same design as the Biocor valve, a bioprosthetic heart valve that is supported by 20 years of published durability data and 25 years of clinical experience.Designed for durability and enhanced control
The Epic Mitral valves triple composite design and unique pericardial shield are designed for durability.
The Epic Mitral valve also features the FlexFit system, which helps facilitate the implant procedure.
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LEFT VENTRICULAR ASSIST SYSTEM

Respect the Flow
The HeartMate 3 left ventricular assist system (LVAS) is designed to provide mechanical circulatory support to a broad range of advanced heart failure patients. Building on proven results from the CentriMag Pumps, the HeartMate 3 LVAS employs Full MagLev flow technology designed to optimize hemocompatibility and reduce blood trauma through gentle blood handling.
In the CE Mark clinical trial, the HeartMate 3 LVAS patients had a 98-percent survival rate at 30 days and 92 percent at 6 months.1 Most saw significant improvements in symptom reduction and quality of life.1
The HeartMate 3 LVAS is indicated for destination therapy, bridge-to-transplantation and myocardial recovery.
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CATHETER PUMP

High Flow, Low Profile
The HeartMate PHP Catheter Pump is an acute percutaneous heart pump designed to stabilize hemodynamically compromised patients undergoing high-risk percutaneous coronary intervention (PCI).
The catheter-based pump is designed for percutaneous entry through the femoral artery. Upon insertion via a low-profile 14F introducer sheath, the catheter is advanced into the left ventricle where the cannula is unsheathed and fully expands to 24 F, allowing for near-full physiological mean blood flow rates.1 The cannula collapses again for removal when the outer sheath is pushed to collapse it.
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PATIENT CARE NETWORK

This device is commercially available for use in select international markets.
Quick and Easy Patient Management
Merlin.net Patient Care Network (PCN) is a remote follow-up system that imports and manages cardiac information for your patients with St. Jude Medical implanted devices. The system allows you to upload and manage patient-device data by accessing a web interface using the Internet and a compatible browser.
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Integrated System

Optimize Every Patient, Every Day
Designed to optimize percutaneous coronary intervention (PCI), the OPTIS integrated system provides precisely the information you need, where and when you need itfor more informed decision-making, greater efficiency and improved procedural effectiveness, especially in patients with complex lesions. Only St. Jude Medical offers a solution that combines both fractional flow reserve (FFR) combined with optical coherence tomography (OCT) technologies to optimize treatment decisions.
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RE-COLLAPSIBLE INTRODUCER

Portico Solo Is Smallest*, 1
The Portico Solo re-collapsible introducer, when it is used with the Portico delivery system, has the smallest TAVI insertion profile (OD and ID), *, 1 enabling smooth navigation and precise trackability.
Designed to reduce vessel trauma in tortuous anatomy.
Designed to minimize access trauma by inserting at a low profile and expanding to a predictable operating profile.
Compatible with the Portico delivery system and available in two sizes: 11 F (ID) and 12 F (ID
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ELITE NONRECHARGEABLE IPG

Pain Relief Without Disruption. Today and Tomorrow.
Improve your patients spinal cord stimulation (SCS) experience with the Proclaim Elite SCS systema nonrechargeable SCS system to provide both St. Jude Medical Burst and tonic stimulation in one system.1 Featuring an advanced recharge-free generator and familiar Apple mobile digital devices, the Proclaim Elite SCS system offers patients a low maintenance option so they can focus less on the system and more on a life with less pain.
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QUADRA ALLURE

More Options to Make Non-Response a Non-Issue
The Quadra Allure MP CRT-P brings MultiPoint pacing, an exclusive St. Jude Medical technology, to cardiac resynchronization therapy pacemakers (CRT-Ps). MultiPoint pacing has proven to elevate cardiac resynchronization therapy (CRT) response.1 St. Jude Medical has built on the quadripolar standard of care to offer more pacing options for your patients.
Quadra Allure MP CRT-P allows patients to undergo MRI scans when used with MRI Ready leads from St. Jude Medical. This device has been tested for safe performance of an MRI scan using a 1, 5 T (Tesla) field-strength MRI scanner.a
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INTEGRATED FFR SYSTEM

Free Your Cath Lab With Wireless FFR
The wireless design of the QUANTIEN integrated FFR system allows you to configure your cath lab environment exactly the way you likefree of clutter from cables. Easy installation gives you full fractional flow reserve (FFR) integration without time-consuming setup or lab downtime.
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Multi-Electrode Radiofrequency Probe

Multi-Electrode Radiofrequency Probe
Enter a new era of performing radiofrequency (RF) ablation for chronic pain management with our Simplicity Probe. A self-contained, patented SI denervation solution, 1, 2 the Simplicity probe features three independent active areas to generally reduce procedure time. It is designed for denervation of the sacroiliac region, including peripheral nerves at S1S4. You will not need an introducer.
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JUDE MEDICAL INFINIT

Inspired by Patients, Engineered With Physicians
The smallest bilateral primary cell IPG on the market, 1 the St. Jude Medical Infinity DBS IPG delivers proven therapy for the management of movement disorder symptoms associated with Parkinsons disease, essential tremor and dystonia. Combine the St. Jude Medical Infinity IPG with advanced directional lead technology and wireless clinician and patient programmers for one of the most advanced DBS platforms available.
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INVISIBLE TRIAL SYSTEM WITH BURST

Invisible. Intuitive. Improved.
The St. Jude Medical Invisible Trial System provides an intuitive way for you and your patients to evaluate spinal cord stimulation (SCS) therapy for managing chronic pain. By eliminating external cables and incorporating Bluetooth wireless technology and Apple mobile digital devices, the system is easier and less burdensome for patients to usegiving them the ability to focus on evaluating SCS therapy instead of managing the system.
This system is also the first trial system to allow patients to evaluate both tonic and our Burst stimulation. If you have patients who have not responded to tonic stimulation in the past, this system gives them the opportunity to try new Burst stimulation.
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PACING LEAD

vPacing Lead for Full-Body, High-Power MRI Scans
The Tendril MRI lead offers unique design advantages to allow patients to undergo full-body, high power 1.5T MRI scans.* Now, your pacemaker patients can have access to the diagnostic benefits that MRI scans provide.
MRI Ready
When combined with the Assurity MRI, Endurity MRI or Accent MRI pacemaker, the Tendril MRI lead:
Allows full-body, 1.5T MRI scans without scan exclusion zones
Permits a maximum whole body averaged specific absorption rate (SAR) up to 4 Watts per kilogram (Wkg)
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STS PACING LEAD

This device is commercially available for use in select international markets.

Advanced Lead Technology Designed for Reliable Performance and Long-Term Durability
We designed the Tendril STS lead to deliver reliable performance through a unique soft silicone tip technology that offers more compliance and less lead tip pressure. The proprietary St. Jude Medical Optim lead insulation featured on the Tendril STS lead offers a minimized risk of lead abrasion and provides long-term durability. Tendril STS lead allows patients to undergo MRI scans when used with an MRI Ready pacemaker from St. Jude Medical.*
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RF ABLATION GENERATOR

Setting New EP Standards With More User Control and Customization
The Ampere RF ablation generator delivers precise radiofrequency (RF) energy and sets a new standard in the electrophysiology (EP) lab with more user control and customization. Designed to improve efficiency and provide seamless connectivity to other St. Jude Medical lab equipment, the Ampere RF generator is a smart choice for your RF ablations.*
Excellent RF efficiency and control
Designed for efficiency and low noise interference, the Ampere RF generator offers you:
Enhanced control with user-selectable power** or temperature modes
Ease of use and quick operation with a color LCD screen for:
Monitoring real-time temperature and impedance data
User presets for increased lab efficiency
Optional remote control module for increased staff efficiency
Included footswitch for bedside physician control
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ELLIPSE

A New Angle on Performance and Safety
The Ellipse ICD is built for the real world. Physicians showed us and told us what they wanted most from an ICD: patient safety and comfort. We turned those ideas into the Ellipse ICD.
Small, physician-designed shape
Up to 36 J delivered energy
Robust ShockGuard technology
Therapy assurance
MR Conditional
Friction-reducing Parylene coating (some models)
Merlin@home transmitter compatible
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Transmitter

BSolutions for Complete Care
Designed to streamline your workflow and support informed clinical decisions, the Merlin@home transmitter works with the Merlin.net Patient Care Network (PCN) for easy and efficient remote care patient management.
Efficient remote care management
The Merlin@home transmitter allows efficient remote care management of patients with implanted cardiac devices through scheduled transmissions and daily alert monitoring. You can complement or replace in-clinic visits with remote patient transmissions.
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RADIOFREQUENCY GENERATOR

The Complete RF Solution
The next evolution in radiofrequency (RF) generators, the NT2000iX RF generator is designed to deliver lesion, pulsed or pulsed dosed treatments to painful nerve sites for chronic pain management. Its fully independent RF amplifiers enable real-time temperature monitoring and reduce the potential for unwanted patient stimulation. The system is designed for ease of use and to give you more control during RF ablation procedures.
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X GUIDEWIRE

Closing the Workhorse Performance Gap With Improved Steerability
The innovative PressureWire X guidewire with flat core technology is the worlds only wireless pressure guidewire for fractional flow reserve (FFR) measurement.1-5 With a new, more durable soft tip design that provides better shape retention and reshapeability6, the PressureWire X guidewire is designed to reduce risk of vessel trauma7 while retaining extraordinary agility, even in tortuous anatomies. The hydrophilic coating significantly lowers friction and enables smoother stent delivery and better overall
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DRG IMPLANTABLE PULSE GENERATOR

Treat More Patients With Better Results1
St. Jude Medical offers the only neuromodulation system approved to stimulate a cluster of nerves called the dorsal root ganglion (or DRG). DRG stimulation expands the range of neurostimulation options you can offer, and allows you to treat patients with focal chronic intractable pain in specific anatomical locations such as the foot, knee, hip and groin.
The Proclaim DRG implantable pulse generator (IPG) neurostimulator system sets a new standard of care for treating chronic intractable pain by providing clinically superior therapy*, 1 in our technologically advanced Proclaim DRG platform.
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IMPLANTABLE PULSE GENERATOR

Two Therapies. One Device. Safe for MRIs.*

The Prodigy MRI implantable pulse generator (IPG) is an MR Conditional device with both our proprietary St. Jude Medical Burst and tonic stimulation, providing more patients with the opportunity for maximum therapy effectiveness. Now patients who may require access to an MRI scan can also access the benefits of Burst technologya proven, patient preferred option to manage chronic pain.1, 2
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  • Eric Eichelberger (St. Jude Medical)
  • 16125 SW 72nd Avenue Portland, OR 97224, United States
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