A wound therapy device is disclosed. The wound therapy device may include a housing for covering at least a portion of a wound and for sealing to a body surface of a patient. The housing may also include a liquid collector for retaining liquid therein and a vacuum connection for coupling to a vacuum source. The vacuum connection may be in gaseous communication with the liquid collector. The vacuum connection may be separated from the liquid collector by a liquid barrier.

A sedation device has a housing divided internally into a ventilator chamber and an associated evaporator chamber which overlap and are separated by a filter mounted between the chambers and forming a common gas-permeable dividing wall between the chambers. An inlet port is provided at one end of the ventilator chamber at a top of the housing for connection to a patient ventilator in use. An outlet port on the evaporator chamber can be connected via a breathing tube to a patient. An evaporator is mounted within the evaporator chamber for delivery of a volatile sedative into the evaporator chamber during use.

The invention relates to a blood treatment device for carrying out an extracorporeal blood treatment in which blood is guided in a blood guidance device having a main blood line and at least one secondary line, the latter being fluidically connected to the main blood line and the main blood line having a dialyzer and, downstream from the dialyzer, a blood treatment element, wherein the blood treatment device has a control device; and a pump configuration, which is equipped for generating blood flows in the main blood line and also in the at least one secondary line, wherein the control device is designed to operate the pump configuration in such a way that a first blood flow rate in the dialyzer is decoupled from a second blood flow rate in the blood treatment element. Furthermore, the invention relates to a blood guidance device for cooperation with the blood treatment device as well as for a blood treatment system.

One aspect of the invention relates to an intubation aid (10). The intubation aid (10) comprises an elongated main part (12), and the intubation aid (10) is provided with an operating device (26). The main part (12) is designed to be curved in a first region (18) of the main part (12), and the main part (12) is additionally designed to be curved in a second region (20) of the main part (12), said second region being separated from the first region (18) and being arranged adjacently to the free end (16) of the main part (12). The main part (12) additionally comprises a positioning device (24) which is designed to limit a translational displacement of a tube (46) placed on the intubation aid (10) in at least one direction. A second aspect of the invention relates to an intubation aid which can be placed on an endoscope.

Provided is a filtering facepiece respirator. The respirator includes a mask body having an anterior side portion, a posterior side portion, a middle portion, a first side portion, a second side portion, a top side portion, a bottom side portion and outer edge portions. The respirator further includes a primary port positioned at the anterior middle portion of the mask body and a detachable primary port adapter which is positioned over and engages the primary port. The respirator may further include an oxygen port and oxygen port adapter and a luer port and luer port adapter.

A device for preventing contamination of a positive-pressure connector (6) of an indwelling needle and a method based on same. The device comprises a shell (1), a connecting port (3) fixedly connected to the shell (1) and used for connecting to the positive-pressure connector (6), an air pressure balance hole (5) disposed opposite to the connecting port (3) and provided on the shell (1), and a filtering membrane (2) provided between the air pressure balance hole (5) and the connecting port (3). The device is simple in structure, adopts a structural design of the filtering membrane (2), can filter microorganisms, bacteria, viruses, dusts, and particulate pollution sources, and is used during indwelling of infusion intervals to prevent the positive-pressure connector (6) from being exposed to the air and maintain the aseptic state and positive-pressure condition of the positive-pressure connector (6) during indwelling.

An infectious aerosol capture mask (IACM) includes a face tent coupled to a suction tube adapter. The face tent includes a proximal opening configured to be disposed over the mouth and nose of a patient. The face tent further includes a distal opening with a smaller diameter than the proximal opening. A coupler is configured to secure the suction tube adapter to the distal opening of the face tent. The suction tube adapter includes a suction port configured to be coupled to a suction tube for active capture of infectious aerosol and left unconnected for passive capture of infectious aerosol. A viral filter is disposed between the suction port and the face tent to capture infectious aerosols expelled by the patient. The IACM further includes one or more one-way valves that are configured to permit airflow into the face tent.

Described herein is a respiratory care apparatus capable of performing multitude of therapy for secretion management and breath assistance therapy. The respiratory care apparatus comprises an electromechanical air router assembly (EARA) and an interfacing assembly. The EARA includes independent first and second pressure generating sources for assisted inhalation/insufflation and assisted exhalation/exsufflation process. The interfacing assembly includes a patient interface port and a patient interface tube. The and negative pressure at the patient interface port for assisted inhalation/insufflation and assisted exhalation/exsufflation processes respectively. The assisted inhalation/insufflation and assisted exhalation/exsufflation processes are carried out independently through separate conduits/passages to reduce contamination and infection. Further, the respiratory care apparatus comprises a garment which oscillates due to alternate positive and negative pressure generation and provides therapy to the patient.

A portable suction pump for aspirating secretions from a patient's artificial airway includes a peristaltic pump head, a suction tube extending from a patient through the peristaltic pump head, the suction tube having a tee-fitting conduit, and a collection container having a plurality of ports for collecting patient media. A clinician has an ability to increase or decrease vacuum levels without increasing or decreasing flowrate and/or an ability to increase or decrease the flow rate without increasing or decreasing the vacuum levels. The tee-fitting conduit extends to a vacuum sensor port connecting to a vacuum sensor in communication with a processor, the processor controlling a proportional valve employed to regulate the vacuum levels.

The present invention is a nebulizer, aerosol, filter or inhalant handheld system. The device is composed of a non-invasive respiratory circuit with a medication reservoir that has an inlet that is configured to be connected to a gas source. In some embodiments, they include of one or more valves located downstream of the medication reservoir. Some embodiments include one or more filters, such as a bacterial viral filter located on the end of the exhalation port. The valve functions to prevent backflow of exhaled air and/or potential pathogens into the atmosphere. The filter functions to significantly reduce the dispersion of aerosols exhaled into the atmosphere and prevent further spread of potential pathogens. Some embodiment may include one or more pivotable elements allowing some portions of the nebulizer to pivot relative to other members.