IN-DATE
MDT37642: Medtronic Patient Programmer for Deep Brain Stimulation (DBS)
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| Price: | $293.50 per box of 1 |
|---|---|
| Quantity: | |
| In Stock: | 12 box of 1 |
| Status: | Non-sterile |
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Additional Details
Medtronic DBS Patient Programmer
For Deep Brain Stimulation
- Model 37642 Patient Programmer
- Carrying Case
- "AAA" batteries (2)
- Product Literature
Patients with an Activa® PC, Activa RC, or Activa SC neurostimulator may use the Medtronic DBS patient programmer to check their neurostimulator status and choose from multiple physician-determined therapeutic options.
The DBS patient programmer has two modes: simple and advanced. The mode and its settings are clinician-determined on an individual patient basis and can be changed at any programming session.
- Simple Mode — Simple mode allows the patient to check the status of his or her deep brain stimulation device without making any therapy changes.
- Advanced Mode — Advanced mode gives the physician the ability to set up four therapy groups with different stimulation parameters. The patient can toggle between groups and adjust therapy within physician-defined limits. If permitted to do so, the patient can adjust rate, amplitude, and pulse width.
AccessGUDID Info
- FDA Product Code: NHL
- FDA Product Code Name: STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS
- FDA Product Code: MRU
- FDA Product Code Name: implanted subcortical electrical Stimulator (motor disorders)
- FDA Product Code: OLM
- FDA Product Code Name: Deep brain stimulator for obsessive compulsive disorder (OCD)
- FDA Product Code: MHY
- FDA Product Code Name: STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR
- FDA Product Code: PJS
- FDA Product Code Name: Stimulator, electrical, implanted, for essential tremor
- GMDN Term Code: 61393
- GMDN Term Name: Multiple active implantable device programmer
- GMDN Term Description: An external, portable, non-dedicated, electrically-powered device intended to change, noninvasively (i.e., wirelessly), the operating parameters (programs) of multiple types of implanted electronic devices (e.g., multiple types of pulse generators); it may in addition program the external trial device used prior to the implanted one. It includes controls (e.g., graphical user interface), integrated software, and a wireless communication transmitter and receiver. It typically also provides historic and/or current information regarding the performance of the implant.
Manufacturer
Medtronic Cardiovascular Therapies offers a broad range of solutions for treating peripheral artery disease, aortic aneurysms, deep vein thrombosis, and other vascular conditions. Key technologies include the Endurant II and Endurant IIs stent graft systems for abdominal aortic aneurysms, the IN.PACT Admiral drug-coated balloon for femoropopliteal disease, and the Abre venous self-expanding stent system for iliofemoral venous outflow obstruction. With a commitment to advancing minimally invasive therapies, Medtronic’s vascular innovations help restore blood flow, reduce procedural risk, and improve quality of life for patients with complex vascular disease.
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