CPC A61N 1/36071 (2013.01) [A61B 5/0022 (2013.01); A61B 5/0031 (2013.01); A61B 5/0538 (2013.01); A61B 5/1118 (2013.01); A61B 5/14539 (2013.01); A61B 5/24 (2021.01); A61B 5/389 (2021.01); A61B 5/40 (2013.01); A61B 5/4824 (2013.01); A61B 5/4836 (2013.01); A61N 1/0551 (2013.01); A61N 1/0553 (2013.01); A61N 1/0558 (2013.01); A61N 1/36125 (2013.01); A61N 1/37229 (2013.01); A61N 1/37235 (2013.01); A61N 1/37288 (2013.01); A61N 1/3787 (2013.01); A61N 2/002 (2013.01); A61N 2/006 (2013.01); A61N 2/008 (2013.01); G16H 40/67 (2018.01); A61B 2560/0219 (2013.01); A61B 2560/0242 (2013.01); A61N 1/36007 (2013.01); A61N 1/36057 (2013.01); A61N 1/36064 (2013.01); A61N 1/36067 (2013.01); H02J 50/00 (2016.02)] | 18 Claims |
1. A neuromodulation apparatus comprising:
an implantable device configured to stimulate tissue, the implantable device comprising:
a resistor configured to measure leakage of the implantable device during a period of non-stimulation to provide single-point failure protection for the implantable device;
a first current source; and
a second current source,
wherein the implantable device is configured to ensure charge balance safety in stimulating the tissue by maintaining an active charge balance between the first and second current sources by matching the first and second current sources to operate in an H-bridge-like configuration, and
wherein the second current source is weaker than the first current source and a stimulation current of the tissue is determined by a current of the second current source; or
wherein the first and second current sources are cascoded and have parallel impedances of at least 1 Mohm.
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