Healthcare Professionals

Verify Evaluation System

Sacral Neuromodulation

Evaluation, Evolved

The enhanced Verify™ evaluation system includes a user friendly mobile platform that helps clinicians evaluate the potential for relief with the InterStim™ system.



InterStim Therapy for Urinary Control is indicated for the treatment of urinary retention and the symptoms of overactive bladder, including urinary urge incontinence and significant symptoms of urgency-frequency alone or in combination, in patients who have failed or could not tolerate more conservative treatments.

This therapy is not intended for patients with mechanical obstruction such as benign prostatic hypertrophy, cancer, or urethral stricture.


InterStim Therapy for Bowel Control is indicated for the treatment of chronic fecal incontinence in patients who have failed or are not candidates for more conservative treatments.

Product Details

Verify Delivers Greater Insight

Verify Evaluation System app usage graph shown on Samsung phone.

The enhanced Verify evaluation system provides data about the system and the evaluation, leading to a well-informed assessment of Sacral Neuromodulation as a treatment option.

  • Tap Into Transparency: Compare patient feedback with actual usage data to help interpret evaluation results.
    • See amplitude settings
    • Identify the program/lead
    • Check if therapy was on/off
  • Confirm System Integrity: The Verify system performs an automatic system integrity check to provide assurance that cable and lead connections are secure.
  • Expedite Efficiency: Streamline setup with Intuitive menus and standardized programs.
    • Choose from 7 preset programs
    • Select how many programs patients can access
    • Create custom programs for unique patient needs

Verify Provides Freedom for Patients

Verify Evaluation System app Program 1 screen shown on Samsung phone.

The enhanced Verify evaluation system includes a simple programmer and a small, concealable external neurostimulator (ENS).

  • Discreet: The ENS weighs less than 2 ounces, is worn on a belt, and is easy to conceal under clothing. Leads are hidden under bandaging.
  • An Easy Experience: The simple, intuitive programmer display makes it easy for patients to turn therapy on or off, or make therapy changes you request.

External Neurostimulator Model 353101

Verify External Neurostimulator Model 3531

The Verify external neurostimulator (ENS) is a small, lightweight, programmable device that pairs with the programmer and delivers stimulation through the lead.

  • Single-patient use device
  • Small
  • Lightweight (less than 2 oz.)
  • Single button, used for On-Off
  • Water-resistant
  • Wireless connectivity with programmer


Verify Evaluation System app home screen shown on Samsung phone.

The programmer used with the external neurostimulator (ENS) that delivers stimulation through the lead.

  • Reuseable device
  • Wireless connectivity with neurostimulator
  • Touch-screen display
  • Usage log
  • Accurate battery estimates
    • Programmer
    • Neurostimulator
  • Single On-Off button
  • Up/down keys increase/decrease stimulation level
  • Virtual dial to control desired amplitude during lead placement
  • Automatic error detection
  • Automatic cable detection
  • Options for standard and custom evaluation programs

Lead Placement Within Verify Clinician App

Watch how to place a lead within the clinician app for the Verify system.


Basic Evaluation

  • Test Stimulation Lead Kit Model 309101
  • Test Stimulation Lead Model 305901 (for bi-lateral placement)

Advanced Evaluation

  • Lead Introducer Kit Model 355018
  • Tined Lead Kit Model 3889
  • Test Stimulation Cable Model 357501/357506
  • Twist Lock Cable (25 cm/64 cm) Model 357625/357644


Access prescriber, implant, MRI, and other manuals on the Medtronic Manual Library. Search by the product name (Verify) or model number (353101). You may also call 800-961-9055 for a copy of a manual.