A neonatal pneumothorax decompression device is disclosed. The device comprises a needle stabilizer, a pressure indicator, and a fluid evacuation pump. The needle stabilizer is configured to facilitate insertion of the needle into a subject's pleural cavity and to hold a needle at an adjustable length. The pressure indicator is coupled to the proximal end of the needle stabilizer and is configured to visibly display pressure within the subject's pleural cavity. The fluid evacuation pump is configured to be actuated by a user to evacuate air or fluid from the subject's pleural cavity through the needle. The fluid evacuation pump is proximally coupled to the pressure indicator and the needle stabilizer.

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.

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 needle assembly for treating tension pneumothorax includes an elongated needle disposed within an elongated catheter, and a housing for containing the needle and catheter. The needle is coupled to the housing through a length adjustment mechanism so that the needle and the catheter are configured to be deployed out of the distal end of the housing to a pre-determined length. The length adjustment mechanism may include an axial path in the wall of the housing, grooves extending off of the axial path, and a protruding arm coupled to the needle. The protruding arm of the needle is configured to extend through the axial path of the housing and be grasped by a user to deploy the needle and catheter out of the distal end of the housing. When the needle is deployed to a desired length, the user may lock the needle and catheter in place by positioning the protruding arm in the corresponding groove extending off of the axial path.

A method and device are provided for simultaneously or near-simultaneously diagnosing and treating tension pneumothorax and/or hemothorax. A Veress-type needle portion includes a hollow needle for puncturing the chest wall over a blunt hollow probe biased by one or more springs to extend distally into the pleural cavity. Openings in the blunt hollow probe connect via a pathway to an automatic check valve, which permits the flow of air and/or fluid only in a proximal direction. Pressure from within the pleural cavity is transmitted to the interior surface of a pressure documenter. If pressure greater than atmospheric pressure is present in the pleural cavity, the pressure documenter will be automatically urged proximally to simultaneously allow air and/or fluid to escape from the pleural space through the device, thus treating the tension pneumothorax and/or hemothorax, as well as providing a stable indicator to positively document the diagnosis of increased pressure.

A method and device are provided for simultaneously or near-simultaneously diagnosing and treating tension pneumothorax and/or hemothorax. A Veress-type needle portion includes a hollow needle for puncturing the chest wall over a blunt hollow probe biased by one or more springs to extend distally into the pleural cavity. Openings in the blunt hollow probe connect via a pathway to an automatic check valve, which permits the flow of air and/or fluid only in a proximal direction. Pressure from within the pleural cavity is transmitted to the interior surface of a pressure documenter. If pressure greater than atmospheric pressure is present in the pleural cavity, the pressure documenter will be automatically urged proximally to simultaneously allow air and/or fluid to escape from the pleural space through the device, thus treating the tension pneumothorax and/or hemothorax, as well as providing a stable indicator to positively document the diagnosis of increased pressure.

The present invention relates to 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, a second reservoir, 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 present invention relates to 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, a second reservoir, 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.

A device includes a base and a tube clamp. The tube clamp is coupled to an upper surface of the base. The assembled tube clamp and base are positioned around a tube and moved into engagement with a surface of a patient, at which point a lower surface of the base is adhered to the surface of the patient to anchor the tube relative to the surface of the patient.

A device includes a base and a tube clamp. The tube clamp is coupled to an upper surface of the base. The assembled tube clamp and base are positioned around a tube and moved into engagement with a surface of a patient, at which point a lower surface of the base is adhered to the surface of the patient to anchor the tube relative to the surface of the patient.