PRODUCT CATALOG

Chronic Pain Therapies | Spinal Cord Stimulation | Charging Systems and Accessories

Prodigy™ Neurostimulation Charging System featuring BurstDR™ Stimulation

3730

Description

Model 3730

Product Highlights

Compatibility

  • Prodigy MRI™ IPG Model 3772
  • Prodigy MRI™ Patient Programmer Model 3856
  • Rapid Programmer™ Programming Device Model 3835
Prodigy™ Neurostimulation Charging System featuring BurstDR™ Stimulation


Ordering Information

Reorder Number Dimensions (H x W x T, cm) Weight (g) Battery
3730 7.3 (Height) x 12.9 (Length) x 3.2 (Thickness) 218 (no wand)
322 (w/wand)
Rechargeable Li+
Reorder Number Description
1245 Charger case
3713 AC power adapter
3714 AC line cord
3731ANS Replacement charger body
3732ANS Charger Antenna, 36-in
7240 Charger belt
7241 Charger pouch

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

 

CE marking does not necessarily indicate regulatory approval status for all markets. Please refer to the instructions for use for a full listing of indications, contraindications, warnings and precautions.

 

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). Clinicians manual must be reviewed for detailed disclosure.

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-0115-0008(1)

Last Updated: October 4, 2016