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1485 results about "Sterilization process" patented technology

A sterilization process is a combination of the sterilizer (including the sterilizer agent), the process, the load, the loading pattern and the wrapping (system).

Food product surface sterilization apparatus and method

InactiveUS20040052702A1Increase temperatureReduce food product temperature changeFood preservationIndirect heat exchangersUnsafe conditionUltraviolet
An apparatus is disclosed for the micro-organism surface sterilization of foods using, a "germicidal" such as light waves (e.g., ultraviolet), and in some cases in combination with (or replaced by) one or more of sound waves and ozone. The surface sterilizer apparatus may include a plurality of germicidal (e.g., ultraviolet) emitters for surface sterilization of foods that are, e.g., rotated in a drum or rotated via a screw auger. Assemblies of emitters for the germicidal may be constructed to be watertight (i.e., withstand a high pressure, heated water spray), and movable relative to the drum or screw conveyor for easy cleaning and maintenance. The apparatus may also include a controller (e.g., programmable logic controller) for controlling the sterilization process so that the apparatus does not endanger personnel nearby, and so that the food is properly sterilized. The controller may vary the amount of germicidal used, the rate that food traverses the apparatus, the inclination of the apparatus, and terminate sterilization processing when an unsafe condition is detected. The apparatus may be used in-line with other food processing equipment for the real-time sterilization of food. The controller may also communicate with food processing components upstream of the apparatus for controlling the flow of food to the surface sterilizer
Owner:C & S EQUIP COMPANY

Sterilization method and apparatus

A method of sterilizing an article by sequentially exposing the article to hydrogen peroxide and ozone is disclosed. The article is exposed under vacuum first to an evaporated aqueous solution of hydrogen peroxide and subsequently to an ozone containing gas. The exposure is carried out without reducing the water vapor content of the sterilization atmosphere, the water vapor content being derived from the aqueous solvent of the hydrogen peroxide solution and from the decomposition of the hydrogen peroxide into water and oxygen. The complete sterilization process is carried out while the chamber remains sealed and without removal of any component of the sterilization atmosphere. For this purpose, the chamber is initially evacuated to a first vacuum pressure sufficient to cause evaporation of the aqueous hydrogen peroxide at the temperature of the chamber atmosphere. The chamber is then sealed for the remainder of the sterilization process and during all sterilant injection cycles. Keeping the chamber sealed and maintaining the hydrogen peroxide and its decomposition products in the chamber for the subsequent ozone sterilization step results in a synergistic increase in the sterilization efficiency and allows for the use of much lower sterilant amounts and sterilization cycle times than would be expected from using hydrogen peroxide and ozone in combination.
Owner:STRYKER CORP

Sterilization container capable of providing an indication regarding whether or not surgical instruments sterilized in the container were properly sterilized

A sterilization container for sterilizing at least one surgical instrument. The container includes at least one sensor for measuring an environmental characteristic of the container during the sterilization of the instrument. The measure of the environmental characteristic is supplied to a processor. The processor compares the measurement of the container environment to a validated measurement for the sterilization process. If the measured environmental characteristic is at least equal to the validated sterilization process measurement, the processor presents an indication that the surgical instruments was properly sterilized.
Owner:STRYKER CORP

Method of sterilizing a medical procedure kit containing a medical adhesive

A medical procedure kit incorporates one or more surgical tools necessary to perform at least part of a medical procedure, along with a container having a quantity of a medical adhesive. Medical adhesives are useful as an alternate or an adjunct to surgical sutures and / or staples in wound closure, as well as for covering and protecting surface wounds such as lacerations, abrasions, burns, stomatitis, sores, minor cuts and scrapes, and other wounds. As such, the inclusion of such an adhesive into a composite medical procedure kit can be of great assistance to a medical doctor or surgeon by providing in single kit form, tools necessary to complete many medical procedures, without having to use multiple procedure kits. The adhesive may be independently sterilized and wrapped from the other surgical tools of the resultant kit, and then associated into kit form, or assembled and sterilized together as a unitary kit. When the adhesive is incompatible with sterilizing procedures of the other components of the kit, the adhesive may be pre-sterilized and protected by a sterilization barrier that shields the adhesive from exposure to the sterilization process used to sterilize other tools of the procedure kit. The adhesive is preferably a 1,1 -disubstituted ethylene monomer, such as an alpha-cyanoacrylate.
Owner:CLOSURE MEDICAL

Method and apparatus for validation of sterilization process

An apparatus, system and method for verifying the achievement of a desired sterility assurance level (SAL) for components manipulated within a low-energy electron beam sterilization chamber. The components are preferably pre-sterilized and connected together in an assembly fashion which creates and maintains the sterility of the connection by subjecting the components to low-energy (less than 300 KeV) electron beam radiation. The verification is completed by measuring the sterilization dose delivered to a sensor, also known as a dosimeter, positioned within the sterilization process to simulate the components.
Owner:BAXTER INT INC

Vapor phase decontamination process biological indicator evaluator resistomer (BIER) vessel

A BIER vessel evaluates biological indicators for sterilization processes. By flowing gaseous sterilant, such as vaporized hydrogen peroxide, through a chamber (12) before, during, and after introducing the indicators, the indicators are instantaneously exposed to preselected steady state conditions, allowing accurate and reproducible evaluation of the indicator response. A door (32) to an opening (30) in the chamber opens for introducing the indicators to the chamber without appreciably disturbing the steady state conditions therein. After a preselected time, the biological indicators are removed and evaluated for remaining biological activity.
Owner:AMERICAN STERILIZER CO

Supercritical carbonic anhydride wall-breaking method for melissa powder

ActiveCN101268815ARemove the effect of active ingredientsImprove permeabilityFood shapingFood preparationExhaust valveAdditive ingredient
The invention discloses a method using supercritical carbon dioxide to perform bee pollen broken-face. Bee pollen is put in an extraction plant of supercritical carbon dioxide, to react for a certain time in supercritical carbon dioxide liquid at the proper pressure and temperature, a vent valve is opened to rapidly empty carbon dioxide, so that a pollen cell expands acutely due to larger pressure difference of the inside and the outside, thereby cracking. The method has the advantages that the operation is simple and convenient, the cost is low, the whole process is performed below 50 DEG C, the broken-face time does not exceed 30 minutes, the influence of the product by thermotropy is reduced, so that the active ingredient is preserved completely, at the same time, bacillus can be killed, the unification of the broken-face and the sterilization processes is realized, the broken-face ratio of the pollen cell is high, but the percentage of damage is low, and the inclusion still exists in a cracked pollen wall under the dry condition, thereby favoring the preservation of the nutritious content.
Owner:陕西康泰莱生物医药工程有限公司
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