PRODUCT CATALOG

Chronic Pain Therapies | Spinal Cord Stimulation | Programmming Platforms (SCS)

Rapid Programmer™ Clinician Programming Device with BurstDR™ Stimulation

3834

Description

Model Number 3834

Product Highlights

Compatibility

  • Prodigy MRI™ Neurostimulation System Model 3772
  • Protégé MRI™ Neurostimulation System Model 3771
  • Protégé™ Neurostimulation System Model 3789
  • Eon Mini™ Neurostimulation System Model 3788
  • EonC™ Neurostimulation System Model 3688
Rapid Programmer™ Clinician Programming Device with BurstDR™ Stimulation


Ordering Information

Reorder Number Dimensions (H x W x T, cm) Weight (g) Battery
3834ANS 13.38 x 7.54 x 2.41 238.00 3800 mAh, lithium ion, rechargeable, removable battery
Reorder Number Description
3823ANS Bluetooth® wireless technology printer
1304ANS Car charger
1627ANS MTS™ joining sleeve
1626ANS Stylus
1629ANS Extended battery
1622ANS Power adapter
1303ANS Battery for Bluetooth® wireless technology printer
1321ANS Power adapter for Bluetooth® wireless technology printer

*BurstDR™ stimulation, patented technology exclusively from St. Jude Medical, is also referred to as Burst stimulation in clinical literature.

 

Rx Only

 

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

 

Indications for Use: Spinal cord stimulation as an aid in the management of chronic, intractable pain of the trunk and/or limbs, including unilateral or bilateral pain associated with the following: failed back surgery syndrome and intractable low back and leg pain.

 

Contraindications: Patients who are unable to operate the system or who have failed to receive effective pain relief during trial stimulation.

 

Warnings/Precautions: Diathermy therapy, implanted cardiac systems, magnetic resonance imaging (MRI), explosive or flammable gases, theft detectors and metal screening devices, lead movement, operation of machinery and equipment, postural changes, pediatric use, pregnancy, and case damage. Patients who are poor surgical risks, with multiple illnesses, or with active general infections should not be implanted.

 

Adverse Effects: Painful stimulation, loss of pain relief, surgical risks (e.g., paralysis). Product technical manual must be reviewed for detailed disclosure.

 

Bluetooth is a registered trademark of Bluetooth SIG, 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.

©2018 St. Jude Medical, Inc. All rights reserved.

SJM-PRD-0616-0035a

Last Updated: October 4, 2016