Cogentix Medical Urgent PC Treatment Steps

Neuromodulation system

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Treatment Steps

For complete instructions for use, storage, warnings, indications, contraindications, precautions, adverse reactions and disclaimer of

warranties, please refer to the insert accompanying each Urgent PC product or online at www.cogentixmedical.com.

Step 1: Check Battery

Prior to beginning treatment, check battery level. To turn on the

stimulator, hold down the Power button for two seconds. Change battery

when there is only one line remaining in the Battery icon. Turn off

Stimulator.

Step 2: Locate Needle

Insertion Site

On the inner leg, use the width of 3

fingers to measure approximately 2

inches from the center of the ankle

bone (2A). Move the top finger back

3/4 - 1 inch (2B). Your finger should

be positioned just behind the tibia.

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Page 1 3/4 - 1 inch (2B). Your finger should be positioned just behind the tibia. For complete instructions for use, storage, warnings, indications, contraindications, precautions, adverse reactions and disclaimer of warranties, please refer to the insert accompanying each Urgent PC product or online at www.cogentixmedical.com.
Page 2 Electrode on the inside arch of the foot on the treatment leg. For complete instructions for use, storage, warnings, indications, contraindications, precautions, adverse reactions and disclaimer of warranties, please refer to the insert accompanying each Urgent PC product or online at www.cogentixmedical.com.
Page 3 For complete instructions for use, storage, warnings, indications, contraindications, precautions, adverse reactions and disclaimer of warranties, please refer to the insert accompanying each Urgent PC product or online at www.cogentixmedical.com.
Page 4 Urgent PC is indicated for the treatment of Overactive Bladder and associated symptoms of urinary urgency, urinary frequency and urge incontinence. CONTRAINDICATIONS: Treatment with Urgent PC is contraindicated for patients with pacemakers or implantable defibrillators, patients prone to excessive bleeding, patients with nerve damage that could impact either percutaneous tibial nerve or pelvic floor function, or patients who are pregnant or planning to become pregnant during the duration of the treatment.