A blood purification device includes a blood circuit for extracorporeally circulating blood of a patient; a liquid supply line for supplying a supply liquid to a blood purifier provided on the blood circuit or to the blood circuit a peristaltic liquid supply pump provided on the blood circuit or on the liquid supply line; a peristaltic waste liquid pump provided on a waste liquid line through which a waste liquid is discharged from the blood purifier; a water balance amount detection unit for detecting a water balance amount of the supply liquid and the waste liquid; and a water balance amount control unit that corrects one or both of pump speeds of the liquid supply pump and the waste liquid pump so that the water balance amount detected by the water balance amount detection unit matches a target water balance amount. The water balance amount control unit is configured to be able to switch between a first correction condition for correcting the pump speed on every water balance amount detection and a second correction condition for correcting the pump speed based on a plurality of water balance amount detection results.

An intravenous (IV) catheter system may include a catheter adapter having a proximal end and a distal end. The IV catheter system may also include a cannula extending through the catheter adapter. A proximal end of the cannula may include a notch. The IV catheter system may also include a needle hub, which may be coupled to the proximal end of the catheter adapter. The needle hub may include a flashback chamber, which may be in fluid communication with the notch when the IV catheter system is in an insertion configuration.

A method includes disposing a lumen-defining device within a portion of a vein of a patient. A support member is inserted into a lumen of the lumen-defining device and advanced through at least a portion of the lumen of the lumen-defining device. At least a portion of the lumen-defining device is supported via the support member such that the support member limits complete occlusion of the lumen in response to a force exerted on the lumen-defining device. A volume of bodily fluid is withdrawn from the patient via the lumen-defining device when the support member is disposed in the lumen-defining device.

Examples of a module for housing unrelated electronic and electromechanical equipment for use during surgery. The module can include a lower section and a tower-like upper section. The lower section can house unrelated electronic and electromechanical equipment. The tower-like upper section can be located on top of the lower section. A water-resistant cowling can enclose at least a portion of the lower section and the tower-like upper section. A cartridge containing one or more ultraviolet-C producing lights can be protectively housed within the tower-like upper section. The cartridge containing one or more ultraviolet-C producing lights can be configured to emerge upward from a top of the tower-like upper section to substantially seat itself on the top of the tower-like upper section when activated allowing the ultraviolet-C light to disinfect the patient and staff-contacting upper surfaces of the equipment in the operating room.

Provided is a filter apparatus, comprising two or more filter cartridges having a first end with an inlet and screen and a second end with an outlet and screen, and walls to contain a filter media held in a housing for holding the two or more filter cartridges in about the same orientation, and an attachment clamp connected to the housing. Also provided is a housing for holding two or more filter cartridges in about the same orientation and a method of using the filter apparatus and housing.

Examples of a module for housing unrelated electronic and electromechanical equipment for use during surgery. The module can include a lower section and a tower-like upper section. The lower section can house unrelated electronic and electromechanical equipment. The tower-like upper section can be located on top of the lower section. A water-resistant cowling can enclose at least a portion of the lower section and the tower-like upper section. A cartridge containing one or more ultraviolet-C producing lights can be protectively housed within the tower-like upper section. The cartridge containing one or more ultraviolet-C producing lights can be configured to emerge upward from a top of the tower-like upper section to substantially seat itself on the top of the tower-like upper section when activated allowing the ultraviolet-C light to disinfect the patient and staff-contacting upper surfaces of the equipment in the operating room.

Aspiration syringes and methods thereof are disclosed. An exemplary aspiration syringe can include a barrel, a plunger disposed in the barrel, and an aspiration mechanism. The aspiration mechanism can include a thumb-support member coupled to a distal portion of the barrel and a syringe housing slidably disposed around the barrel. The syringe housing can include a proximal portion coupled to a proximal portion of the plunger and a distal portion terminating with a flange incorporated into a finger-support member. The aspiration mechanism can be configured for withdrawing the plunger from the barrel as the finger-support member is slid over the barrel toward the thumb-support member. An example method of the foregoing aspiration syringe can include a fluid-aspirating step including aspirating fluid from a fluid-containing space with a single hand over a medial portion of the syringe by squeezing together the finger-support member and the thumb-support member.

Provided is a filter apparatus, comprising two or more filter cartridges having a first end with an inlet and screen and a second end with an outlet and screen, and walls to contain a filter media held in a housing for holding the two or more filter cartridges in about the same orientation, and an attachment clamp connected to the housing. Also provided is a housing for holding two or more filter cartridges in about the same orientation and a method of using the filter apparatus and housing.

According to an embodiment, a medical device is disclosed. The medical device includes an external unit and an implantable unit. The external unit includes an electronic unit operationally coupled to a transmitter coil that is configured transmit power and/or data signal over a wireless transcutaneous link, a coil unit comprising a loop structure with the transmitter coil being wound around and along at least a part of length of the loop structure, and a fixation unit configured to attach the loop structure to a user's body i) proximal to an implantable receiver coil that is configured to be implanted within a body part, and ii) around a body part of a user such that a part of the body part is positioned in a hollow section of the loop structure. The implantable unit includes the implantable receiver coil configured to receive the power and/or data signal over the wireless transcutaneous link, a processing unit configured to i) process the received data signal to control functionalities of at least one of the components of the implantable unit, and/or ii) utilize the received power for operation of at least one of the components of the implantable unit. The wireless transcutaneous link includes a coupling between the transmitter coil and the receiver coil, and when the loop structure is attached using the fixation unit, at least a substantial number of magnetic field lines generated in response to excitation of the transmitter coil passes through the implantable receiver coil.

A suction head adaptor suitable for collecting fluid and blood during a surgical operation is provided. The suction head adaptor includes a first end and a second end opposite from the first end. The suction head adaptor may have a conical structure at the first end with a first aperture positioned at a center of the conical structure. A tube extends from the first aperture toward the second end and has a second aperture at the second end, allowing fluid to flow from the first aperture to the second aperture through the tube. An absorbent material such as a gauze can be provided within the conical structure. A splash guard can be provided on the tube to prevent splashing during suction, and ridges can be provided on the tube at the second end to allow the suction head adaptor to be inserted into a suction tube connected to an aspirator.