A method for sealing a tissue opening includes inserting a trocar tube including a folded sealing device disposed within the trocar, and guiding the trocar tube through an opening in a myocardium into a patient's ventricle, the sealing device can include an elongated elastic member having a distal and a proximal end, a proximal umbrella shaped braiding extending radially from the elongated elastic member, the proximal braiding being positioned at the proximal end of the elastic member, wherein the proximal braiding includes a proximal disc disposed therein having a proximal disc thread disposed therethrough such that a user can pull the proximal braiding, and a distal umbrella shaped braiding extending radially from the elongated elastic member and being positioned at the distal end of the elastic member opposite to the proximal braiding.

A degradable cardiac pacing current-providing wire, comprising: conductive core; insulating film ,covering said conductive core, wherein said conductive core is made of magnesium alloy, the weight percentage of said magnesium alloy is: zinc 4.5-5.5%, manganese 0.8-1.2%, calcium 0.8-1.2%, and the remainder is magnesium, said insulating film is made of either or at least two copolymers of Polylactic acid (PLA), Polyglycolic acid (PGA), Polycaprolactone (PCL), Polydioxanone (PDS) and Polyhydroxyalkanoate (PHA). A cardiac pacing current-providing unit, for use in providing pacing current to the heart of the patient, comprising: wire; suture needle and connecting electrode which is connected to the cardiac pacemaker, there is no wire residue in the body after degradation, and no metal artifacts will occur, which makes the patients free from the need for re-operation, and reduces the mental, physical and economic burden caused by the operation, has a strong clinical application value.

A defibrillation system with a unique paddle assembly. The paddle assembly has a paddle head with a conductive surface. The paddle head is introduced into the chest through a small surgical incision. The paddle head is connected to a handle by an elongated shaft. The elongated shaft has an electrically conductive core that is covered in a dielectric insulator. The elongated shaft is malleable. A pivot connection joins one end of the elongated shaft to the paddle head. The pivot connection enables the paddle head to move through a range of different orientations with respect to the elongated shaft. Electricity passes through the conductive core of the elongated shaft and into the paddle head.

Representative embodiments of the present invention provide for novel, minimally invasive implantable devices and methods for targeted tissue drug delivery of cardiovascular drugs.

A percutaneous lead assembly for an active implantable device, the lead assembly comprising a sheath with a plurality of wires extending from a proximal end to a distal end. The wires being adapted to power the active implantable device; the distal end having at least one electrode fixed thereon. The electrodes being in communication with sensor electronics and wherein at least one electrode is on the outer layer of the lead assembly in which the electrode is used to detect at least one of acceleration and electrical signals of an organ.

A connector block that permits simultaneous and continuous interconnection of the three leads of the epicardial pacing wires, the pacemaker, and the ECG monitor on clear separately labeled connectors is provided. Circuitry is provided that allows the display of epicardial signals on the telemetry unit, while still preserving the ability to pace the heart from the pacemaker. When pacing the connector block prevents excessive loading of the pacer signals by the ECG monitor and/or damage to the monitor by the high-voltage pacer signals. The connector block may be used universally on all monitors without the need for sophisticated understanding of the electrical characteristics of the ECG monitor or concern for damage or improper signal loading.

A stimulation device includes an energy source; an electronics unit; an actuator that is coupled with the electronics unit and/or the energy source. The electronics unit includes a controller. The energy source, the electronics unit and the actuator are arranged in a housing. A fixing unit which is coupled with the housing and affixes the stimulation device on a heart or in a heart. The actuator emits electromagnetic waves for the stimulation of genetically manipulated tissue, and the controller controls the stimulation of the tissue by way of the electromagnetic waves of the actuator.

An implantable device for implantation in a human body or animal body. The device includes an energy source, an energy storage device, and an electronics unit. Further, an actuator is coupled with the energy storage device and it is configured to emit electromagnetic waves by discharging the energy storage device.

A stimulation device contains an energy source, an electronics unit, and an actuator that is coupled with the electronics and/or the energy source. The actuator is configured to emit electromagnetic waves for stimulation of genetically manipulated tissue. The stimulation device is configured for at least temporary implantation in the human or animal body. The electronics unit has a controller configured to stimulate the tissue by use of the electromagnetic waves from the actuator.

A stimulation device has an energy source, an electronics unit with a controller, a fixing unit and an actuator that is coupled with the electronics and/or the energy source. The actuator is configured to emit electromagnetic waves for stimulation of genetically manipulated tissue. The stimulation device is configured for at least temporary implantation in a human or animal body. The controller is configured to control the stimulation of the tissue by use of the electromagnetic waves of the actuator. The stimulation device has a control unit that picks up data that characterizes the tissue activity and/or the success of a stimulation by a stimulation carried out through the electromagnetic actuator.