Description
Medtronic 3058 Interstim II Neurostimulator for Bladder and Bowel Control
Part # 3058 Exp 2/19
The Medtronic 3058 Interstim II system delivers sustained improvements in quality of life for people with overactive bladder (OAB), non-obstructive urinary retention, and chronic fecal incontinence (FI).
The neurostimulator streamlines the implant procedure with a design that eliminates the need for the lead extension and uses fewer set screws.
- Connects directly to the lead, eliminating need for an extension
- Accommodates three lead sizes: 28 cm, 33 cm, and 41 cm
- Compatible with a lead insertion indicator in the lead
- Integrates strain relief in the header
- Incorporates radiopaque identification of manufacturer and model number
- Allows 1-screw implantation
Medtronic 3058 Interstim II SYSTEM COMPONENTS
- Tined lead model 3889
- InterStim smart programmer for clinicians
- InterStim smart programmer for patients
- TYRX neuro absorbable antibacterial envelope
BLADDER CONTROL CANDIDATES
Many patients with OAB or retention have poor or reduced quality of life because of their symptoms. These patients are considered suitable for the InterStim™ system once they have failed or could not tolerate more conservative treatments.
This therapy is appropriate for bladder control patients who:
- Experience urge incontinence or urgency-frequency
- Experience urinary retention without an obstruction
- Need another option if medication does not provide symptom relief and/or causes unpleasant side effects
- Want an alternative to repeated injections
This therapy is not appropriate for bladder control patients who:
- Experience primarily stress incontinence
- Have not demonstrated an appropriate response to the InterStim™/therapy evaluation
- Are unable to operate mobile devices (such as the smart programmer for the InterStim™ system)
- Are not appropriate candidates for surgery
- Experience retention due to obstructions (such as BPH, cancer, or urethral stricture)
BOWEL CONTROL CANDIDATES
Many patients with chronic FI have poor or reduced quality of life because of their symptoms. These patients are considered suitable for the InterStim™ system if they have failed (or are not candidates for) more conservative treatments such as medication, behavior modifications, bowel retraining, and/or pelvic muscle training.
This therapy is most appropriate for bowel control patients who:
- Have frequent bowel accidents
- Experience urge incontinence and/or passive incontinence
- Need another option if medication that does not provide symptom relief and/or causes unpleasant side effects
This therapy is not appropriate for bowel control patients who:
- Have not demonstrated an appropriate response to the InterStim™/therapy evaluation
- Have issues using mobile devices (such as the smart programmer for the InterStim™ system)
- Are not appropriate candidates for surgery
In Perfect sealed condition but past expiration date. Not for human use in the US.
Expiration dates have mostly to do with sterilization and not the integrity of the product. The manufacturers sterilize the products after they are packaged and it lasts so many years. The only products we caution customers about are ones that are absorbable or drug coated.