| CPC A61B 18/1445 (2013.01) [A61B 2018/00345 (2013.01); A61B 2018/00595 (2013.01); A61B 2018/0063 (2013.01); A61B 2018/1455 (2013.01); A61B 34/30 (2016.02); A61B 2034/301 (2016.02)] | 20 Claims |

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1. An in-vivo vessel sealing end effector, the end effector comprising:
(a) an in vivo end effector body coupleable to an arm of an in vivo robotic device, wherein the arm and the end effector body are configured to be positioned entirely within a cavity of a patient, the end effector body comprising at least one actuator and a cautery component shaft disposed within the body;
(b) a bipolar vessel cautery component operably coupled to the end effector body, the cautery component comprising:
(i) first and second jaws disposed at a distal end of the cautery component shaft; and
(ii) a cutting component moveably coupled to the cautery component shaft;
(c) an electrical connection disposed on the cautery component shaft, wherein the electrical connection is electrically coupled to one of the first and second jaws;
(d) a first slip ring disposed within the end effector body, wherein the first slip ring is electrically coupled with the electrical connection during rotation of the cautery component shaft;
(e) a second slip ring disposed within the end effector body, wherein the second slip ring is electrically coupled with the cautery component shaft during rotation of the cautery component shaft; and
(f) an external electrical source electrically coupled to the first and second slip rings;
wherein the at least one actuator comprises a cautery component rotation actuator operably coupled to the cautery component shaft.
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