An implantable device for improving the pump function of the heart of a human patient by applying an external force on the heart muscle. The device comprises at least one pump device comprising a heart contacting organ, an operating device for operating the heart contacting organ, and an implantable pressurized fluid system. The fluid system comprises a first implantable chamber adapted to hold a pressurized fluid, wherein said first chamber is adapted to hold a fluid having a high pressure and a second implantable chamber adapted to hold a pressurized fluid, wherein said second chamber is adapted to hold a fluid having a lower pressure. The movement of the heart contacting organ assists the pump function of the heart.

A single use pleural drainage set for medical use, which allows drainage by all physicians of air (pneumothorax), blood (hemothorax) and all other liquids (hydrothorax) accumulated abnormally in the thoracic cavity (pleural space (I)).

A single use pleural drainage set for medical use, which allows drainage by all physicians of air (pneumothorax), blood (hemothorax) and all other liquids (hydrothorax) accumulated abnormally in the thoracic cavity (pleural space (I)).

An improved method and device are provided for forming and/or maintaining a percutaneous access pathway. The device generally comprises at least one of three type of components: access pathway, insertion device, and attachment device. In one embodiment, the device is used to form and/or maintain a percutaneous access pathway into the pleural cavity (i.e. tube thoracostomy). The provided assembly substantially reduces the possibility of iatrogenic infection while accessing and/or re-accessing a body space.

An improved method and device are provided for forming and/or maintaining a percutaneous access pathway. The device generally comprises at least one of three type of components: access pathway, insertion device, and attachment device. In one embodiment, the device is used to form and/or maintain a percutaneous access pathway into the pleural cavity (i.e. tube thoracostomy). The provided assembly substantially reduces the possibility of iatrogenic infection while accessing and/or re-accessing a body space.

An implantable device for improving the pump function of the heart of a human patient by applying an external force on a first position of the heart muscle following the heart's contractions. The implantable device comprising a first pump device adapted to assist the pump function of the heart. The pump device comprises a first reservoir having a first volume and adapted to varying said first volume, a second reservoir having a second volume and adapted to varying said second volume, a fluid connection adapted to fluidly connect said first reservoir with said second reservoir, such that fluid can flow between said first reservoir and said second reservoir. The reservoir, said second reservoir and said fluid connection form a fully implantable pump device adapted to maintain a fluid in a closed system, when in operation and wherein said fully implantable pump device is adapted to transfer force by transferring fluid from said first reservoir to said second reservoir to directly or indirectly apply an external force on the first position of the heart muscle, following the heart's contractions, for improving the pump function of the heart, when said device is implanted. The implantable device further comprises a sensor sensing muscle contractions of the heart.

An implantable device for improving the pump function of the heart of a human patient by applying an external force on a first position of the heart muscle following the heart's contractions. The implantable device comprising a first pump device adapted to assist the pump function of the heart. The pump device comprises a first reservoir having a first volume and adapted to varying said first volume, a second reservoir having a second volume and adapted to varying said second volume, a fluid connection adapted to fluidly connect said first reservoir with said second reservoir, such that fluid can flow between said first reservoir and said second reservoir. The reservoir, said second reservoir and said fluid connection form a fully implantable pump device adapted to maintain a fluid in a closed system, when in operation and wherein said fully implantable pump device is adapted to transfer force by transferring fluid from said first reservoir to said second reservoir to directly or indirectly apply an external force on the first position of the heart muscle, following the heart's contractions, for improving the pump function of the heart, when said device is implanted. The implantable device further comprises a sensor sensing muscle contractions of the heart.

A system, method and apparatus for performing a thoracostomy comprises a tube for insertion in a patient's chest cavity, an inflatable sac configured on a first section of the tube, an inflation valve for inflating the inflatable sac, and a flange associated with a second section of the tube configured for securing the tube wherein the first section of the tube is inserted into the patient's body and the second section of the tube is external to the patient's body.

A system, method and apparatus for performing a thoracostomy comprises a tube for insertion in a patient's chest cavity, an inflatable sac configured on a first section of the tube, an inflation valve for inflating the inflatable sac, and a flange associated with a second section of the tube configured for securing the tube wherein the first section of the tube is inserted into the patient's body and the second section of the tube is external to the patient's body.

Disclosed are devices and methods for treating tension pneumothorax. A needle assembly may include an outer cannula defining a lumen and having a distal end portion with a sharp bevel, and an inner cannula slidably-disposed through the lumen of the outer cannula. The inner cannula moves between an extended and retracted position and includes a blunt distal end portion configured to extend beyond the sharp bevel of the outer cannula when the inner cannula is in the extended position. The blunt distal end portion can retract within the lumen of the outer cannula when the inner cannula is in the retracted position, thereby exposing the sharp bevel. The needle assembly further includes a bias disposed inside the housing and coupled to the inner cannula. A proximal end portion of the inner cannula is configured to extend through the housing when the inner cannula is in the retracted position.