A barrier for use in negative pressure wound therapy can include a base layer and surface structures. The barrier can be used to reduce or prevent tissue ingrowth. A method of using a negative pressure wound therapy system can include positioning a perforated barrier in a wound. After positioning the perforated barrier in the wound, positioning a pad in the wound on top of the perforated barrier, positioning a seal on top of the wound to at least partially seal the perforated barrier and the foam in the wound, and applying negative pressure wound therapy to the wound.

An operable implant adapted to be implanted in the body of a patient, the operable implant comprising an operation device and a body engaging portion, wherein the operation device comprises a first unit comprising a receiving unit for receiving wireless energy and a first gear system adapted to receive mechanical work having a first force and first velocity, and output mechanical work having a different second force and a different second velocity. The operation device further comprises a second unit comprising an electrical motor adapted to transform electrical energy to the mechanical work, and a distance element adapted to separate the first and second units such that the receiving unit, when receiving wireless energy, is not substantially affected by the second unit.

This disclosure provides apparatus and methods for detecting pressure changes within a cavity of a patient. A pressure-sensing catheter comprises an elongate member and a monitor lumen. The pressure-sensing catheter may have a hollow pressure-compliant member in fluid communication with the monitor lumen and thereby define a fluid column. A connector apparatus can be in fluid communication with the monitor lumen, and can comprise a first complementary connector and a second complementary connector. One of the first complementary connector and the second complementary connector can have a pressurizing device that can displace a volume of fluid located within a bore of the other complementary connector into the fluid column, wherein the ratio of the volume of displaced fluid to the volume of the fluid column ranges from about 1:2 to about 1:4. The pressure catheter can comprise a radio-opaque band circumscribing the exterior of the elongate member.

Various embodiments of a double cuff single lumen endotracheal tube device for lung isolation and protection and its method of use are described herein. A device for intubation providing for single lung isolation and a transition to ventilation of both lungs is described. In one example, the device can be used extend into a main bronchus of patient. A distal cuff and secondary cuff can be inflated for ventilation of one lung. An auxiliary conduit provides passive oxygenation to the non-ventilated or alternately evacuation of mucus or fluids above the distal cuff. The device can be repositioned for long term intubation and ventilation of both lungs.

The present application relates to an outlet graft for a blood pump as well as to a system comprising a blood pump and an outlet graft that is connected to an outlet of the blood pump. The outlet graft includes a first end opposite a second end such that a longitudinal axis is formed between the first and second ends. The second end is connectable to a blood vessel and a lumen with a closed cover. A first strip included in the cover extends parallel to the longitudinal axis and is made of a material that is of a higher contrast under x-rays than the cover.

A minimally invasive miniaturized percutaneous mechanical circulatory support system for transcatheter delivery of a pump to the heart that actively unloads the left ventricle by pumping blood from the left ventricle into the ascending aorta and systemic circulation. The pump may include a tubular housing, a motor, an impeller configured to be rotated by the motor. The impeller may be rotated by the motor, via a shaft with an annular polymeric seal around the shaft, or via a magnetic drive. The system may have an insertion tool having a tubular body and configured to axially movably receive the circulatory support device, and an introducer sheath configured to axially movably receive the insertion tool.

A device for sealing a tracheostoma in a patient includes a seal member for insertion through the tracheostoma to a trachea. The seal member includes a disc having a predetermined line of weakness. In a first configuration, the seal member forms a seal by being pulled against the tracheostoma. In a second configuration, the seal member is removed from the trachea through the tracheostoma by breaking along the line of weakness.

An anesthetized catheter that includes the ability to administer substances and remove substances via the catheter orifice as well as pericatheter with the option of using wireless technology, while also having an indication system.

A method of fixating an implantable heart help device in a human patient is provided. The method comprises the steps of: cutting the skin of said human patient, dissecting an area of the body comprising bone, and fixating said implantable heart help device to said part of the body comprising bone.

A sheath for producing a fully sealed access to the interior of a vessel of an animal or human body comprises a base sheath having a tubular body defining a pass-through channel. The base sheath is adapted to be inserted into the vessel through a vessel aperture. The sheath further comprises an expansion device which is adapted to cooperate with the base sheath such that the outer diameter of the sheath increases in the region of the vessel aperture with the sheath in a stationary position in the vessel and upon actuation of the expansion device.