Patent classifications
A61M2205/36
INJECTION DEVICE STORAGE CONTAINER
An injection device storage container includes a case configured to contain at least one injection device for delivering a medicament; and a hanger arrangement coupled to the case and configured to suspend the case from a supporting wall; wherein the case includes an upper panel having an opening formed therein through which the at least one injection device can be dispensed, and wherein the opening is arranged such that, when the case is suspended from the supporting wall, the at least one injection device is dispensed in a horizontal orientation through the opening.
CONTROLLED POROSITY DEVICES FOR TISSUE TREATMENTS, METHODS OF USE, AND METHODS OF MANUFACTURE
In various embodiments, a device is provided comprising a balloon configured to expand to an expanded state in response to introduction of a fluid at a first pressure, wherein the fluid perfuses through the balloon above a second pressure, the second pressure being the same or greater than the first pressure. In various embodiments, a method comprising fabricating a balloon configured to expand to an expanded state in response to introduction of a fluid at a first pressure, wherein the fluid perfuses through the balloon above a second pressure, the second pressure being at or greater than the first pressure, disposing the balloon on an elongate member having a lumen, placing the lumen in fluid communication with an interior volume of the balloon.
METHOD OF HEAT SANITIZATION OF A HAEMODIALYSIS WATER CIRCUIT USING A CALCULATED DOSE
A method of sanitizing liquid for use in a medical device, the method comprising the steps of providing a medical device defining a water circuit with a volume of liquid, sensing the temperature of the volume of liquid with a sensor, heating the volume of liquid from an initial temperature to exceed a threshold temperature, maintaining the volume of liquid above the threshold temperature, determining a time-temperature value for the volume of liquid periodically once the threshold temperature has been exceeded, calculating a cumulative time-temperature value and providing an output signal once the cumulative time-temperature value has reached a level indicative of a sanitizing dose. A medical device and a liquid sanitizer are also disclosed.
A SYSTEM AND A METHOD FOR PRODUCING MICROBIOLOGICALLY CONTROLLED FLUID
A method and a system (10a) comprising an integrated water purifying apparatus (110) with a pre-filter circuit (402) including a particle filter and an activated carbon filter arranged to produce pre-treated water; a fluid circuit (404) arranged to receive pre-treated water from the pre-filter circuit (402), the fluid circuit (404) includes an RO-pump (450) and a Reverse Osmosis, RO, device, (301) arranged to produce purified water; a heating device (302) arranged to heat purified water from the RO device (301) to a temperature above 65°; the water purifying apparatus (110) is further arranged to heat disinfect the fluid circuit (404) using the heated purified water. The system (1) further comprises a line set (40) connected to the purified water outlet connector (128) at a water line connector (68) of the line set (40), wherein the line set (40) includes at least one sterile sterilizing grade filter (70a, 70b) arranged to filter the purified water into sterile purified water.
COATED ANESTHETIC CONTAINER FOR AN ANESTHETIC DISPENSER AND MANUFACTURING PROCESS
A coated anesthetic container for an anesthetic dispenser includes an anesthetic tank, which is capable of receiving a liquid anesthetic (Nm), as well as a refill unit for refilling liquid anesthetic (Nm). The anesthetic tank includes a wall and a coating on the inner surface of the wall. A wall of the refill unit is connected in a fluid-tight manner to the wall of the anesthetic tank. A coating is applied at least to the inner surface of the wall of the anesthetic tank. This coating is made of an alloy of nickel and phosphorus. The nickel portion is in a range of 80 wt.% to 97 wt.%, and the phosphorus portion is in a range of 3 wt.% to 15 wt.%. A process is provided for manufacturing such an anesthetic container.
STEAM THERAPY EQUIPMENT FOR GOOD HEALTH AND WELLNESS
A steam therapy equipment including a vessel for heating a mixture of water and organic materials, a compressor to inject pressurized air into the vessel producing pressurized steam. The pressurized steam is conducted into the equipment via one or more valves. The therapy equipment is formed from at least one panel and may include a supporting frame. The therapy equipment includes a temperature sensor to measure the temperature inside the therapy equipment when pressurized steam is admitted via the valves. A patient enters the equipment and is exposed to the pressurized steam, causing dilation of the skin pores of the patient, whereby toxins are removed from the patient. One or more applicators may conduct pressurized steam to specific portions of the body of the patient. The patient may be provided with a portion of the mixture to consume as part of the steam therapy treatment.
Breathing assistance apparatus
A breathing assistance apparatus and method of controlling a breathing assistance apparatus is disclosed. Particularly, the breathing assistance apparatus is controlled such that it has a drying cycle to enable drying of the tubing that supplies gases to a user and prevent the harboring of pathogens within the tube. The drying cycle is preferably operated automatically by internal controllers in the apparatus. However, it may be manually activated by pressing a button on the apparatus. The drying cycle is preferably activated at the end of a user's treatment session.
Breathing assistance apparatus
A breathing assistance apparatus and method of controlling a breathing assistance apparatus is disclosed. Particularly, the breathing assistance apparatus is controlled such that it has a drying cycle to enable drying of the tubing that supplies gases to a user and prevent the harbouring of pathogens within the tube. The drying cycle is preferably operated automatically by internal controllers in the apparatus. However, it may be manually activated by pressing a button on the apparatus. The drying cycle is preferably activated at the end of a user's treatment session.
Pump cassette and methods for use in medical treatment system using a plurality of fluid lines
A fluid handling cassette, such as that useable with an automated peritoneal dialysis (APD) cycler device or other infusion apparatus, may include a generally planar body having at least one pump chamber formed as a depression in a first side of the body and a plurality of flowpaths for a fluid that includes a channel. A patient line port may be arranged for connection to a patient line and be in fluid communication with the at least one pump chamber via at least a first one of said flowpaths, and an optional membrane may be attached to the first side of the body over the at least one pump chamber. In one embodiment, the membrane may have a pump chamber portion with an unstressed shape that generally conforms to the depression of the at least one pump chamber in the body and is arranged to be movable for movement of the fluid in a useable space of the at least one pump chamber. One or more spacers may be provided in the at least one pump chamber to prevent the membrane from contacting an inner wall of the at least one pump chamber. The patient line, a drain line, and/or a heater bag line may be positioned to be separately occludable in relation to one or more solution lines that are connectable to the cassette.
Methods and systems for waste gas detection in an anesthetic vaporizer
Systems and methods are provided for detecting and sequestering waste anesthetic gases released by an anesthetic vaporizer. In one embodiment, a method for an anesthetic vaporizer installed in an anesthesia machine includes detecting an emission of waste anesthetic gases (WAGs) from the anesthetic vaporizer, and responsive to detecting the emission of WAGs, performing at least one of scavenging the WAGs and outputting an alert.