The present disclosure relates to a tissue collection apparatus. The tissue collection apparatus comprises a housing defining an inlet and an outlet, a first filter disposed within the housing, a second filter disposed within the housing, the second filter configured to isolate tissue particles of a desired size that pass through the first filter under the application of an aspiration force applied through the housing. A method of harvesting tissue is also disclosed.

Systems and methods for the removal of carbon dioxide from circulating blood via the use of microbubbles within a body cavity, optionally including the simultaneous provision of oxygen to the circulatory system. Through placement of microbubbles within a body cavity and the use of a carbon dioxide scavenging catheter, carbon dioxide and/or oxygen exchange may occur. Overall improvement in extending survival rate time during emergency situations caused by pulmonary or similar ventilation restricting injury and/or failure may be achieved.

A patient interface for treating sleep disorder breathing includes a textile tube that also provides support for the seal forming structure. The textile tube includes an inner and outer layer that are joined along seams to form an air chamber or passageway. The textile tube can be pre-shaped so that the textile tube resiliently returns to a pre-determined shape prior to the introduction of pressurized air.

A patient interface for treating sleep disorder breathing includes a textile tube that also provides support for the seal forming structure. The textile tube includes an inner and outer layer that are joined along seams to form an air chamber or passageway. The textile tube can be pre-shaped so that the textile tube resiliently returns to a pre-determined shape prior to the introduction of pressurized air.

A fluid management system including a pass-through fluid volume measurement system to provide continuous measurement of fluid returned from a surgical site during transit to a waste collection system. The pass-through fluid volume measurement system eliminates the need to physically replace full fluid collection containers during the medical procedure with new, empty fluid collection containers.

A blood treatment system comprising at least one first device and at least one second device, wherein the first device is a membrane filter for the removal of toxic mediators from blood and the second device is suitable for the removal of granulocytes and monocytes from blood. The first device has a first blood flow path a first blood flow path for conducting blood through and the second device has a second blood flow path. The first and second devices are serially connected in succession in such a way that the first blood flow path is in fluid communication with the second blood flow path.

The membrane has an interior filter space in its housing and a semipermeable membrane arranged in the interior filter space, which membrane divides the interior filter space into a retentate chamber and permeate chamber. The housing has a blood inlet device and a blood outlet device that are in fluid communication with the retentate chamber, as well as a permeate outlet for diverting permeate from the permeate chamber. The blood inlet device, the retentate chamber and the blood outlet device form the first blood flow path. The membrane filter has a separation characteristic such that the sieve coefficient for albumin, SK.sub.Alb, is within the range from 0.015 to 0.35.

An insertion instrument includes a shaft projecting, by being inserted through a hole of a fixing instrument, from a distal end of the fixing instrument toward a distal side, and a gas supply channel formed in the shaft section and having a jet port, which jets a gas, in a distal portion of the shaft section. The gas is supplied from a proximal side to the distal side toward the jet port in the gas supply channel, and an extension dimension along the longitudinal axis from the jet port toward the proximal side is greater than an extension dimension of the hole of the fixing instrument.

An insertion instrument includes a shaft projecting, by being inserted through a hole of a fixing instrument, from a distal end of the fixing instrument toward a distal side, and a gas supply channel formed in the shaft section and having a jet port, which jets a gas, in a distal portion of the shaft section. The gas is supplied from a proximal side to the distal side toward the jet port in the gas supply channel, and an extension dimension along the longitudinal axis from the jet port toward the proximal side is greater than an extension dimension of the hole of the fixing instrument.

Kits, devices, systems and related methods for obtaining a nasopharyngeal sample utilize a rinsing fluid supply component and a collecting component, which may be used as separate modules or integrated with a housing to form a handheld unit that may be operated with a single hand. The dispensing component may include a flexible reservoir pump containing a supply of rinsing fluid, and a first nostril interface adapted to engage a first nostril of a patient and guide a stream of rinsing fluid into the patient's nasal cavity. The collecting component may include a collection container and a second nostril interface adapted to engage a second nostril of a patient and collect effluent. An absorbent shield may be arranged on the integrated unit to absorb stray fluid.

Systems and methods for reducing pathogens near an implant are discussed. In some cases, the methods include reducing contaminants in a portion of a patient that has an implant and that is disposed interior to a closed surface of skin of the patient. The method can further include placing a conduit in the closed surface of skin and flowing an antimicrobial fluid into that portion of the patient to contact the antimicrobial fluid with a surface of the implant and tissue adjacent to the implant. In some cases, the antimicrobial fluid is then removed from the portion of the patient having the implant. As part of this method, biofilm near the implant can be mechanically, ultrasonically, electrically, chemically, enzymatically, or otherwise disrupted. Other implementations are described.