Saban Ventures Pty Limited

Michael Potas

Vladimir Berentsveig

Ron Weinberger

Brian Hingley

Sarah Nix

Tara Croft

A cover for a probe, such as an ultrasonic probe, the cover comprising a flexible elongate pouchand a mouth portionfor inserting the probeinto the pouch, the mouth portioncomprising sealing means to enable the mouth portion to be formed into sealing engagement with a proximal endof the probe. Also, a method of preventing a decontaminated ultrasonic probe from contamination comprising the step of, immediately after disinfection, inserting the ultrasonic probeinto a cover comprising a flexible elongate pouchand a mouth portionfor inserting the probeinto to pouch, the mouth portioncomprising a deformably rigid portion, and deforming the mouth portioninto a sealing engagement with a proximal endof the probe, wherein no undisinfected portion of the probeenters the pouch

Probe cover

A nebuliser cup for maintaining a safe level of liquid during nebulization, the cup comprising a liquid level sensor comprising: a first element sensing liquid at or below a position corresponding to a filled liquid level in the nebuliser cup; a second element electrically isolated from the first element and located at a position corresponding to a filled liquid level in the nebuliser cup; and wherein when the cup is not filled with a liquid to the filled liquid level, the first element, the liquid and the second element do not form an electrically coupled circuit; and when the cup is filled with a liquid to the filled to liquid level, the first element, the liquid and the second element together form an electrically coupled circuit.

Liquid level sensor

Methods for determining the amount of residual sterilant remaining on the surface of an object at the end of a disinfection process are described. One method of determining the amount of residual sterilant on a test piece after a sterilization regime in a sterilization space includes the steps of: placing a test piece having a predetermined surface area into the sterilization space; subjecting the test piece to the sterilization regime; collecting the residual sterilant from the test piece in a collector solution; and measuring the amount of residual sterilant in the collector solution.

Residual sterilant test method

A method of sterilizing an object comprising the steps of i) placing an article to be sterilized in a sterilization chamber; ii) providing a sterilizing mist (for example hydrogen peroxide solution) to the sterilization chamber, thereby to contact said article for a first duration; iii) providing a gas flow to said chamber for a second duration, thereby to displace, where present, said sterilizing mist and to remove, where present, condensed mist from said article; wherein the total reduction in micro organisms over a time period encompassing the first duration and the second duration is less than log; and wherein steps ii) and iii) are repeated at least once to achieve a predetermined sterilization parameter such as a predetermined sum total of contact time between the sterilizing mist and the article, a predetermined sum total of sterilizing mist provided to the sterilization chamber or a predetermined level of sterilization.

Sub-cycle based aerosol disinfection system

Methods for disinfecting or sterilizing an article are provided. One method includes vaporizing a solution comprising a biocide in a solvent having a first biocide:solvent ratio, directing a flow of the vapor to a first side of a membrane; directing an alternate flow of a gas to a second side of the membrane to increase the first biocide:solvent ratio on the first side to a second biocide:solvent ratio greater than the first biocide:solvent ratio thereby producing a concentrated vapor on the first side of the membrane, and contacting the article with the concentrated vapor for a time sufficient to disinfect or sterilize it.

Methods of disinfection or sterilization

A method of measuring density of a sterilant aerosol e.g. aqueous hydrogen peroxide, in a gas stream (such as a stream of air) for the purposes of measuring sterilant dosage comprising: passing a gas stream at flow rate past an electrically heated element and measuring a first cooling effect, passing an aerosol suspended in a gas stream at flow rate past an electrically heated element and measuring a second cooling effect and measuring the difference between the first cooling effect and second cooling effect and correlating the difference with aerosol density. The total dosage can thus be determined. A measured dosage of a sterilant aerosol can be delivered by way of a feedback loop to halt further delivery of sterilant aerosol when the amount of aerosol delivered reaches a predetermined dosage. The methods allow sterilization to be certified.

Growing community of inventors

Alexandria, Australia

Michael Potas