A medical/surgical waste collection rover includes a first waste container disposed on a portable cart and receiving waste under the influence of a vacuum. A fluid measuring system includes a float element disposed within the first waste container, and a controller causing liquid in a reservoir disposed on the cart to prefill the first waste container and subject the float element to an initial lifting to a zero point level. The fluid measuring system determines a volume of contents within the first waste container based on a position of the float element relative to the zero point level. The fluid measuring system may include a sensor rod extending through the first waste container and a second waste container disposed on the cart and separated from the first waste container by a transfer valve. Methods of estimating the volume of liquid and/or medical/surgical waste within the waste container are also provided.

A copolymer has blood compatibility and antithrombotic properties of greatly suppressing protein adhesion to be usable even when in contact with a biological component such as blood for a long period of time, and a medical device uses the copolymer. The copolymer is characterized by including a hydrophilic unit and a hydrophobic unit, wherein the hydrophobic unit contains at least one type of a carboxylic acid vinyl unit, and the number of carbon atoms at the terminal of a side chain of the carboxylic acid vinyl unit is 2-7.

To provide a blood treatment filter device capable of efficiently utilizing a blood treatment filter.

A blood treatment filter device 20 has a filter sheet 26 through which a specific component among components forming blood is harder to pass than other components and a spacer sheet 27 through which the specific component is easier to pass than through the filter sheet 26. The filter sheet 26 has filter through-holes 39 disposed at intervals. The filter sheet 26 and the spacer sheet 27 are spirally wound in an overlapped state. The filter device 20 has seals 31 sealing both end portions in the longitudinal direction of a wound body 25 formed by the filter sheet 26 and the spacer sheet 27 which are spirally wound in a fluid-tight manner. The outer peripheral surface of the wound body 25 is formed by the filter sheet 26.

[Object of the Invention] An object of the present invention is to provide a breathing apparatus, wherein current for keeping internal pressure of the face piece at a predetermined positive target value at the time of inhale is not applied to the motor fan in a large amount at the start of current application to the motor fan, and the internal pressure of the face piece is prevented from becoming far below the predetermined positive target value immediately after start of current application to the motor fan so as to keep the internal pressure of the face piece at the predetermined positive target value at the time of inhale.

[Disclosure of the Invention] A breathing apparatus provided with a breath-synchronized motor fan comprising a face piece for covering a part of or all of a face of a user, an inhale valve and an exhale valve attached to the face piece, a motor fan for supplying internal space of the face piece with external air through the inhale valve, a filter for cleaning the external air to be sucked into the motor fan, a breath monitoring apparatus provided with a membrane member deforming in accordance with fluctuation of internal pressure of the face piece and a sensor for detecting the deformation of the membrane member, and a controller for controlling operation of the motor fan synchronously with breathing of the user in accordance with a detection signal from the breath monitoring apparatus, wherein the controller applies current to the motor fan at the time of inhalation so as to keep the internal pressure of the face piece at a predetermined positive target value, and stops current application to the motor fan so as to stop the motor fan at the time of exhalation, and wherein the controller applies micro-current to the motor fan so as to rotate the motor fan at extremely low speed from the middle of exhalation to inhalation.

The invention provides a blood treatment device comprising: a dialyser; an inlet pump assembly; an outlet pump assembly; and a control system. The inlet pump assembly configured to deliver a first volume of dialysate from a dialysate source to the dialyser in an inlet pump cycle having a dialysate delivery stroke. The outlet pump assembly configured to remove a second volume of dialysate from the dialyser and deliver the dialysate away from the dialyser in an outlet pump cycle having a dialysate removal stroke. The control system is configured to operate the inlet pump assembly in the inlet pump cycle, and configured to operate the outlet pump assembly in the outlet pump cycle. For each inlet pump cycle there is a corresponding outlet pump cycle, and each inlet pump assembly dialysate delivery stroke has a commencement time t.sub.1 and a termination time h, and each outlet pump assembly dialysate removal stroke has a commencement time t.sub.3 and a termination time t.sub.4. The blood treatment device is operable such that either: each dialysate removal stroke commencement time t.sub.3 is after the respective corresponding dialysate delivery stroke commencement time ti and before the respective corresponding dialysate delivery stroke termination time t.sub.2; or each dialysate delivery stroke commencement time t.sub.1 is after the respective corresponding dialysate removal stroke commencement time t.sub.3 and before the respective corresponding dialysate removal stroke termination time t.sub.4.

A system and method are provided for controlling fouling and complement protein activation during separation of plasma from whole blood using a spinning membrane separator. The separator includes a pair of relatively rotating surfaces spaced apart to define a gap therebetween, with at least one of the surfaces comprising a membrane that allows plasma to pass therethrough but substantially prevents the passage of red cells. In accordance with the method, the membrane material and membrane fabrication technique are selected so as that the resulting membrane both resists fouling and complement protein activation. In a specific embodiment, the membrane is has a smooth surface and substantially linear pores. The pores have a nominal diameter of less than 2 microns (so as to exclude platelets) and preferably a diameter of from 0.6 microns to 0.8 microns, as may be obtained by use of track-etching. In addition, the membrane material preferably is polycarbonate, as it has been determined that polycarbonate does not activate complement proteins.

Embodiments of the present invention disclose a method of cosmetic or biomedical application of a device, comprising a self-contained syringe device comprising an inner syringe included within an outer syringe and wherein a filter is attached inside the outer syringe barrel; wherein the filter comprises a filter material that prevents premature filter collapse where the filter material is optionally coated to increase stiffness, and wherein liposuctioned adipose tissue is collected and purified inside the syringes.

The device for producing ultrapure water according to the reverse osmosis principle with a reverse osmosis filter which is subdivided by the RO membrane into a primary chamber and a secondary chamber, with a primary circuit through which raw water is supplied to the primary chamber and concentrate is discharged therefrom, and with a secondary circuit for supplying permeate to at least one consumer, preferably to a dialysis device, is characterized in that a means for detecting organic and/or inorganic deposits is arranged in or on the primary circuit and/or the secondary circuit and is connected to an evaluation means.

The present invention provides a porous non mechanical valve which retards or prevents the passage of bodily fluids and is resistant to being occluded or blocked by exposure to the surgical fumes or aerosols encountered during surgical procedures.

A waste collection unit for collecting waste material. First and second waste containers are supported on a portable cart. A control panel is configured to receive one or more inputs of selectively set vacuum levels in the first and/or second waste containers. A control system controls operation of vacuum regulators based on the input(s) to regulate levels of vacuums being drawn in each of the waste containers. Pressure sensors in communication with the control system may be positioned to monitor pressure in the waste containers. A back up port support on the portable cart may be provided to receive a vacuum line for coupling a vacuum manifold to a remote vacuum source not located on the portable cart. Container lamps may be coupled to the first and/or second waste containers and configured to illuminate the waste material within the waste containers to be viewed through transparent windows.