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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 a)&|@a3ix g].3&^.jFMO5a 0000007197 00000 n
Update my browser now. The new Medtronic scanning parameters 1 increases SAR limits for 1.5 Tesla scans from 0.5 W/kg to 2.0 W/kg; and for 3 Tesla scans from 0.5 W/kg to 1.4 W/kg. 0000004045 00000 n
This includes a new B1+rms technology for 1.5Tesla scans, and an updated label that adds more flexibility to clinicians practices. 0000013358 00000 n
Medicare and many other private insurance companies cover Medtronic Bladder Control Therapy. Less information (see less).
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For more information on Medtronic (NYSE:MDT), visit www.Medtronic.comand follow @Medtronic on Twitter and LinkedIn. 0000009912 00000 n
This therapy ismost appropriatefor bowel control patients who: This therapy isnot appropriatefor bowel control patients who: In Perfect sealed condition but past expiration date.
Its also important to note that the updated label is the result of several years of collaborative effort between Medtronic, the Medicines and Healthcare products Regulatory Agency (MHRA), and other MRI device manufacturers.
Always talk with your doctor about diagnosis and treatment information. How sacral nerve stimulation neuromodulation works. 0000005793 00000 n
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NEUROSTIMULATION SYSTEM: INTERSTIM THERAPY SACRAL NERVE STIMULATION (SNS) FOR URINARY CONTROL MRI Guidelines for InterStim Therapy Neurostimulation Systems MR Scanning Conditions MR Conditional: Non-clinical testing has demonstrated that InterStim Therapy systems have been found to be MR Conditional. Healthcare Professionals
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Information on this site should not be used as a substitute for talking with your doctor. 0000005042 00000 n
- (06:31), A video of how the InterStim II system electrically stimulates the sacral nerve for bladder control therapy.
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Contact Medtronic at the appropriate address or phone number listed at the back of this manual if you have any questions.
De Wachter S. et al New Technologies and Applications in Sacral Neuromodulation: An Update Adv Ther 37, 637-643 (2020).
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).
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This small electro-optical device is not only a cool-looking device, but it does not affect the quality of your MRI images. .
If this patient is implanted with an InterStim II Model 3058 Neurostimulator or an eligible serial number of an InterStim Model 3023 Neurostimulator (when implanted as a system including a neurostimulator, lead, and, extension as applicable), MRI examinations of the head only may be safely performed, - Maximum spatial gradient of 19 T/m (1900 gauss/cm), - RF transmit/receive head coil only (no RF transmit body coil), - Gradient slew rate limited to 200 T/m/s, - Normal operating mode (Scanning frequency of approximately 64 MHz only), - Model 3058 and eligible Model 3023 Neurostimulators: Turn the neurostimulator, - Eligible Model 3023 Neurostimulators only: Disable the magnet switch, Scanning under different conditions may result in severe patient injury or device. More information (see more) Some of these interactions, especially heating, are potentially hazardous and can lead to serious or permanent patient injury. Treatments & Therapies
Shipping, operating, and power-on-reset (POR) values for the Medtronic InterStim II Model 3058 Neurostimulator a. a All values are approximate. 0000010287 00000 n
The following information describes the potential interactions and control measures that should be taken to minimize the risks from these interactions. This site is Exclusively Sponsored by BRACCO. REFERENCE