Govind Ballabh Pant Hospital Tender

DBS System,Ø Implantable Pulse Generator (IPG) for Deep Brain Stimulation should be available in non -rechargeable or rechargeable versions.,Ø IPG should be dual channel to support 2 leads for bilateral configuration.,Ø IPG should support electrodes with 1.5 mm and 0.5 mm gap between the two contact points,Ø The Extension cable should be available to connect Deep Brain Stimulation lead with Implantable pulse generation.,Ø Extension cable should have stretch coils for better durability and life,Ø IPG should have the facility to program up to 4 different groups of programming with each group having a maximum of 4 different set of programs.,Ø System should have patient programmer to increasing or decreasing stimulation level himself.,Ø System should have the facility to program up to 2 programs per lead.,Ø System should have the facility to choose between constant voltage and constant current power mode. Both options should be available in the same system.,Ø System should be US FDA Approved for Parkinson disease and Essential Tremors.,Ø IPG should also support for Dystonia, OCD and Epilepsy,Ø System should be US FDA approved for MRI Head Scans post implant also.,Ø IPG should have a predictable battery life.,Ø Treatment Planning station and Micro Electrode Recording system should be provide by the company free of cost basis for case support

Intrathecal Pump,Ø The System should be fully implantable for Intrathecal drug delivery. Ø The System should be capable of multiple setting (programming) during 24 hrs to suit patient requirements. Ø Should have the minimum to maximum flow rate between 0.048 ml/day – 24.0 ml/day Ø Should be available in 20 ml reservoir size to be used in pediatric patients having less body mass. Ø Should be available in 40 ml reservoir size for adult patient having sufficient body mass to support the implant. Ø Should have the facility to be refilled subcutaneously through a silicone port. Ø Option of personal therapy manager to give control to the patient for bolus or increase or decrease the dose Ø Refill port to support up to 500 punctures. Ø Should be compatible to 1.5 Tesla MRI conditionally. Ø Should be US FDA approved for Intrathecal use of Baclofen for Spasticity and Morphine Sulphate solution for Pain management

Sacral Nerve Stimulator,Ø System should be US FDA approved for Overactive Bladder and Fecal Incontinence. Ø Should be indicated also for Non Obstructive Urinary retention. Ø Should be compatible with Tined Lead for better grip inside the muscles and less lead migration. Ø Should be available in variants supportive with extension and direct lead insertion, both. Ø Should have the facility to program 4 different sets of therapy parameters with a single lead. Ø System should have patient programmer to increasing or decreasing stimulation level himself.