Abstract: A sterilization container has a valve arrangement that remains open in a venting phase and is then closed before a pressure difference is compensated for at a predetermined differential pressure. The valve remains closed until the container is opened for the purpose of withdrawing and using the sterilized instruments contained therein. The valve is actuated through a snap disk arrangement, the snap disks of which vault gradually into opposite directions at predetermined temperatures, thereby effecting a defined valve control. The snap disk arrangement is provided in a thermally isolated housing, which prevents a premature back-switching of certain snap disks that could be caused by a cooling-off as a result of the evaporation of condensate.

Abstract: A high-pressure reactor which has a hydraulically controlled pressure-relief valve. The mechanical design of the corresponding hydraulic system in combination with the control technology used facilitates particularly fast opening of the pressure-relief valve in the case of pressure or temperature jumps in the high-pressure reactor.

Abstract: A pressure cleaning vessel is connected to a vacuum chamber by way of a connecting pipe in the sterilizing and cleaning equipment that utilizes a supercritical fluid. The objects to be treated are impregnated, for a given period, in the supercritical fluid with which the pressure cleaning vessel has been filled. Thereafter, the connection between the pressure vessel and the vacuum chamber is opened so as to generate sudden bubbling within the vessel as a result of a large pressure difference. Thorough sterilization is achieved at the time when the supercritical fluid having penetrated into bacteria and viruses suddenly explodes and destroys these organisms instantly by vaporization and expansion.

Abstract: An apparatus for sterilizing a sealed enclosure (1) includes a fan (8) for circulating a gas through a preparation circuit (11) and through the enclosure. The preparation circuit includes an evaporation chamber (10) for dispensing a decontaminant gas and water vapor mixture into the circulating gas to flow therewith through the enclosure and to reach a concentration in the enclosure above the dew point for the ambient temperature in the enclosure and thereby to condense onto surfaces in the enclosure to sterilize such surfaces. A monitor (15) measures gas temperature and dew point/condensation are monitored (17, 18) in the enclosure. The resulting signals led to a control module (19) for controlling the rate of dispensing of the decontaminant gas and water vapor into the gas in the preparation circuit in response to the levels determined by said monitoring to provide a required level of condensation of the decontaminant gas and water vapor in the enclosure.

Abstract: Exemplary embodiments may include a sanitizing system and method including a chamber, a wet and dry heating system adjacent to the chamber, and a filtered air system to reduce the contaminants entering the system and to provide positive pressure to the chamber to reduce the likelihood of contaminants entering the system.

Abstract: In a process for sterilizing objects, the surfaces of the objects are dampened by condensating a steam compound of water and hydrogen peroxide. The steam compound reaches hereby the objects to be sterilized without any additional transport gas flow. Subsequent drying occurs by means of evacuation at a pressure below the boiling points of water and hydrogen peroxide.

Abstract: A self-contained, single manual step unit for thermally sterilizing dental and medical instruments is disclosed. The unit, which requires only activation of a single manual switch and which controls an autoclaving cycle by monitoring temperature of matter which changes states between solid and liquid at a predetermined temperature, provides an effective autoclaving instrument. In disclosed embodiments, each unit comprises a protective housing with a pressure containing releasible lid, a heated vessel and a cooling assembly. Thermal regulation and autoclaving timing is determined by mass and thermal characteristics of the matter and by an electrical control circuit comprised primarily of electric heaters and thermally controlled switches. Steam for autoclaving is provided by capsules or other water containers disposed within a well of the vessel at the beginning of an autoclaving cycle.

Abstract: A sterilizer including a sterilization chamber for receiving articles to be sterilized and a door supported on a horizontal pivot at an access opening of the sterilizer chamber. The door includes a seal plate and a resilient seal member supported on the seal plate wherein the seal member includes an annular lip extending transversely to the plane of the seal plate. The lip extends into the sterilizer chamber wherein pressure within the chamber exerts a force biasing an opposing surface of the lip into engagement with an inner surface of the chamber. The sterilizer door is movable between a fully closed and a fully open position and includes a mechanism for holding the door in a partially open position. In the partially open position, the lip extends into contact with a surface of the sterilizer chamber to thereby form a bridge between the door and chamber and prevent condensation from dripping down away from the chamber and door.

Abstract: A system for sterilizing or microbially deactivating instruments and devices. The system includes a circulation system for circulating a microbial deactivation fluid through a chamber for containing the instruments and devices. The chamber forms a portion of the circulation system. The system further includes a fluid over-flow/make-up air assembly. The fluid over-flow/make-up air assembly includes a manifold having an inner cavity that is in fluid communication with the circulation system, an overflow port in the manifold, and an overflow valve assembly disposed in the manifold allowing fluid flow from the cavity to the overflow port when a pressure in the cavity exceeds a pressure in the overflow port by a predetermined amount. A filter assembly is attached to the manifold. The filter assembly has a filter valve assembly in communication with the cavity.

Abstract: The system includes an enclosure for providing a closed volume for bactericide vapor. The enclosure has a container access opening formed therein for providing vapor communication between a container and the closed volume. A container interface assembly at the container access opening positions, locks and seals the container to the enclosure. A container door removal system is partially contained within the enclosure and is operably engaged with the enclosure and attachable to a container door of the container for separating the container door from the container. The container door removal system includes an actuator element located external to the enclosure. A vapor injection system is included having an inlet and an outlet for the bactericide vapor.

Abstract: A pressure regulating device for regulating the pressure exerted on a medical instrument in a reprocessor for microbially deactivating the medical instruments.

Abstract: A combination dryer and atomized medicinal liquid apparatus and shoe or boot drying attachment, wherein the apparatus accommodates the placement of a shoe and/or boot drying attachment on an upper surface thereon. The attachment rests upon the upper surface of the dryer and atomized medicinal apparatus covering the air discharge outlets and channeling the generated air through two vertically disposed tubes. The tubes have a fixed end adjacent the attachment and a free end with an opening for transmitting or transferring the air to a shoe or boot placed thereon. A support ring circumscribes the tubes and supports a shoe(s) or boot(s) placed thereon, thereby promoting efficient drying and/or treatment of the shoe or boot by the apparatus and attachment combination.

Abstract: A device for cleaning and sterilizing the inside of a chamber, including a supply of sterilizing liquid for said chamber and a device for inducing variations in the pressure, amplitude, frequency and the gradient of said variations in the sterilizing liquid, whereby said device is adapted in such a way that cavitation occurs inside the liquid, the device inducing said pressure variations include a liquid column between the chamber and a switching organ, whereby the chamber can be cyclically connected to a depression, whereby the value thereof is related to the amplitude or respectively to the atmospheric pressure.

Abstract: Apparatus for the treatment of material comprises a confined volume for receiving the material, and a source of gas at elevated pressure communicable with the interior of the volume. A suitable source of gas is an airgun, or other apparatus capable of releasing a volume of gas at elevated pressure such as at least 1000 psi. It is preferred that the source of gas is located within the confined volume. It is also preferred that the confined volume is a pressure vessel. Inlet an outlet valves will assist in loading and unloading material for treatment. Gate valves will further assist by closing when the volume is full. The invention is thus particularly useful in the destruction of chemical and biological agents, for the purification of contaminated water, and for the destruction of tropical and other larvae previously leading to diseases such as Nile Disease, malaria and the like.

Abstract: A self-cleaning system for delivering sanitized water to a workstation has a boiler which produces heat-sanitized water and steam. A diverter valve permits a fluid delivery line of the system to convey either sanitized water or steam to a workstation. The steam serves to sanitize the delivery line and workstation and removes biofilms therefrom.

Abstract: A pressure regulating device for regulating the pressure exerted on a medical instrument in a reprocessor for microbially deactivating the medical instruments.

Abstract: A heat sterilization process for small, washed, and bagged articles such as vial stoppers includes a conditioning or air removal phase prior to sterilization. During the air removal phase, a substantial majority of the liquid moisture is removed from the bagged articles by introducing brief periods of dry, warm air to the autoclave chamber. The air is introduced in short bursts at the point of greatest vacuum while pressure pulsing the chamber during the air removal phase. The air is heated and injected into the chamber through a supply valve which is rapidly opened and closed while the chamber is maintained within a preselected vacuum range between the pressure pulses. The result is a greatly reduced time for a complete sterilization and drying process.

Abstract: Apparatus and systems serve to collapse steam in effluent released from steam sterilizers and sterilizer systems. These systems include tanks or containers configured for receiving and holding fluids, for example, water, and include a fluid outlet and a port that receives the released effluent. A conduit extending into the tank from the effluent receiving port provides a path for the steam to the fluid in the tank, to collapse the steam.

Abstract: An apparatus for disinfecting and sterilizing dental handpieces includes a treating chamber with an internal holding stub which has through-channels for connecting exterior treatment fluid source elements to internal standard channels in and through the handpieces to through-flush treatment fluid through these channels from a socket end to a tip end of the handpiece. The treating chamber is laid-out as a pressure resistant autoclaving chamber provided with steam generation at elevated temperature and pressure. The through-channels of the holding stub are alternatively connectable through an outlet valve to the exterior atmosphere so as to enable back-flushing of pressurized steam from the treating chamber through the internal channels from the tip end to the socket end.

Abstract: An apparatus and methods for treating dentures at elevated pressured to enhance the effectiveness of the treatment employs a sealed pressure containment vessel. Denture cleaning, disinfecting, deorderizing, brightening, bleaching can be performed using this apparatus and method and the effectiveness of conventional active agents in removing plaque or the biolayer on the surface of the denture can be improved. Active agents can be forced into pores, fissures and microscopic openings in dentures to remove pathogens or contaminants that cannot be reached by conventional processes. The effectiveness of conventional effervescent denture treatment tablets can also be increased.

Abstract: A biosolids treatment system comprising a storage tank for containing a quantity of biosolids sludge, a system of disinfection piping within the storage tank comprised of a segment of inner biosolids piping having a plurality of holes spirally arranged at a desired spacing around its perimeter concentrically arranged with a segment of outer steam piping, delivery pumps for delivering a quantity of biosolids to the storage tank, biosolids pumps for delivering a flow of biosolids from the storage tank to the inner biosolids piping; and steam pumps for delivering a flow of steam to the outer steam piping and thereby injecting a flow of steam from the outer steam piping into the inner biosolids piping for thermally disinfecting the flow of biosolids in the inner biosolids piping. The system includes computerized controls for continuously and simultaneously monitoring and operating the biosolids and steam pump means.

Abstract: An autoclave 41 comprises a chamber 42 in which medical equipment, for example, an endoscope is stored, a steam feeder 43, a vacuum pump 44, and a control unit 45. The steam feeder 43 feeds steam to the chamber 42. The vacuum pump 44 depressurizes the inside of the chamber 42. The control unit 45 controls the steam feeder 43 and vacuum pump 44. The autoclave 41 executes a first depressurization process that includes a step of depressurizing the chamber 42, an autoclaving process which succeeds the first depressurization process and in which the chamber 42 is pressurized, and a second depressurization process that succeeds the autoclaving process and includes a step of depressurizing the chamber 42. The autoclave 41 thus autoclaves the medical equipment stored in the chamber. Even when the medical equipment is autoclaved, deterioration of the internal parts of the medical equipment deriving from humidity can be prevented.

Abstract: This invention relates to table top steam sterilizers, wherein a novel method of heat conservation within the sterilizer, using fixed vacuum chamber walls, is described. As well, the temperature of the sterilizer is more accurately regulated and stabilized by power application to a single heating coil with the use of a proportional controller, and by use of temperature, pressure and humidity sensors. The method also relates to a post-sterilization moisture evacuation process using a venturi. When this method is employed, the time required for the sterilization process is reduced.

Abstract: A combination dryer and atomized medicinal liquid apparatus for feet is provided having a housing with two slightly recessed footprints shaped concavities formed wihtin the top. A plurality of air discharge outlets discharge a pressurized stream of warm air in conjunction with an atomized stream of antifungal or other medicinal liquid upward onto the sole area of the user's feet.

Abstract: This invention relates to a sterilisation apparatus, comprising a sterilisation unit and a processing unit, wherein said processing unit is arranged to control a sterilisation process within said sterilisation unit. In accordance with the invention, said units are mechanically separated from each other, the units being interconnected by means of at least one of an information or medium exchange device.

Abstract: A metering valve for delivering liquids from a reservoir includes a rotatable valve plug having at least one well in the valve plug. The valve plug prevents direct communication across the valve. Rotating the valve plug transfers the liquid from the reservoir into the well on the valve plug. Rotating the valve plug further transfers the liquid in the well from the valve plug to the point of delivery. The rotation of the valve plug can be repeated to transfer more liquid. The metering valve can be used to deliver vaporizable germicides to a sterilization chamber. A single metering valve can be used to deliver varying amounts of vaporizable germicide to different sizes of sterilization chamber by rotating the valve plug an appropriate number of times. The valve plug can contain multiple wells to deliver large volumes of liquid quickly.

Abstract: The system includes an enclosure for providing a closed volume for bactericide vapor. The enclosure has a container access opening formed therein for providing vapor communication between a container and the closed volume. A container interface assembly at the container access opening positions, locks and seals the container to the enclosure. A container door removal system is partially contained within the enclosure and is operably engaged with the enclosure and attachable to a container door of the container for separating the container door from the container. The container door removal system includes an actuator element located external to the enclosure. A vapor injection system is included having an inlet and an outlet for the bactericide vapor.

Abstract: A method for continuous heat sterilization of liquid includes a continuous pre-heating step of preheating the liquid, a final heating step of heating the preheated liquid to reach a predetermined sterilizing temperature, a holding step of holding the liquid which has reached the predetermined sterilizing temperature for a predetermined period of time, and a cooling step of cooling the held liquid. The final heating step comprises the following steps (a) and (b): (a) a step of continuously pressurizing the liquid by a high pressure pump; and (b) a step of releasing the liquid continuously to a normal pressure within a time period of less than 10 seconds after the pressurizing step to thereby make the liquid reach the predetermined sterilizing temperature. An apparatus for automatically carrying out the method is provided. According to the continuous heat sterilization method and apparatus, scorch during the final heating step is dispensed with and accordingly, a long period of continuous operation is feasible.

Abstract: A self-contained, single manual step unit for thermally sterilizing dental and medical instruments is disclosed. The unit, which requires only activation of a single manual switch and which controls an autoclaving cycle by monitoring temperature of matter which changes states between solid and liquid at a predetermined temperature, provides an effective autoclaving instrument. In disclosed embodiments, each unit comprises a protective housing with a pressure containing releasible lid, a heated vessel and a cooling assembly. Thermal regulation and autoclaving timing is determined by mass and thermal characteristics of the matter and by an electrical control circuit comprised primarily of electric heaters and thermally controlled switches. Steam for autoclaving is provided by capsules or other water containers disposed within a well of the vessel at the beginning of an autoclaving cycle.

Abstract: A chemical vapor sterilization process is enhanced by concentrating a germicide via exploitation of the difference between the vapor pressures of the germicide and its solvent. A diffusion restriction can be placed into the diffusion path to assist this process and the path then opened to provide rapid diffusion of the thus concentrated germicide.

Abstract: This invention includes a novel method for safely, effectively and efficiently pooling of tissues for treatment prior to implantation into a recipient in need thereof. In one embodiment, the method includes perfusion of a porous implant which achieves efficient interpenetration of desired factors into and removal of undesirable factors from the pores of the implant, cleaning of the implant, efficient passivation of the implant (inactivation of pathogens, microorganisms, cells, viruses and the like and reduction in antigenicity thereof), and the novel implant produced by such treatment. The process presents a system wherein the rate of pressure cycling, the fact of pressure cycling, and the amplitude of pressure cycling, results in highly cleaned tissues and other implants for implantation.

Abstract: An automated endoscope reprocessor (10) includes a removable rack (12) for receiving a container (16, 16′). The container has a clamshell housing (20) having two mating portions (24, 26). The portions together define an internal pressurizable chamber (56) for receiving an endoscope head (22). The endoscope's connector cord (82) is carried through an outlet (80) to the chamber. The outlet is defined by channels (88, 90), one in each of the two housing portions (24, 26). A gasket assembly in the outlet provides a restricted fluid passage which allows a small portion of fluid to flow through the outlet when the connector cord is positioned therein. The gasket assembly (120) includes a number of resiliently flexible fins (126, 128, 130) positioned in each channel, each fin having a U-shaped slot (144, 146, 148). Pairs of fins overlap such that the slots together define openings (150) of diminishing size.

Abstract: A sterilant challenge device (1), for use in testing the efficiency of the air removal stage of a sterilization cycle in a sterilizer, includes a tube (2) of thermally-insulating material, the bore of which is closed at one end (3) and open at the other for the entry of sterilant. A plurality of thermally-conductive masses (4) is located around the tube (2) and thermally-separated from one another by air gaps (14), and a temperature sensor is located in an opening (16) in one of the masses adjacent the closed end of the tube. An outer casing (5) defines an air space around the thermally-conductive masses and thermally insulates the masses from the heat in the sterilizer.

Abstract: A pressure cleaning vessel 1 is connected to a vacuum chamber P by way of a connecting pipe in the sterilizing and cleaning equipment which utilizes a supercritical fluid. The objects to be treated is impregnated, for a given period, in the supercritical fluid with which the pressure cleaning vessel 1 has been filled. Thereafter, the connection between the pressure vessel 1 and the vacuum chamber P is opened so as to generate sudden bubbling within the vessel 1 as a result of a large pressure difference. Thorough sterilization is achieved at the time when the supercritical fluid having penetrated into bacteria and viruses suddenly explodes and destroys these organisms instantly by its power of vaporization and expansion.

Abstract: Autoclave construction and methods that can substantially reduce shipping costs for large autoclaves. In accordance with the invention, the autoclave body, the door and the hinge assembly for mounting the door to the autoclave body are manufactured as bolt together assemblies, with the autoclave body shipped without the door or hinge assembly attached thereto. This reduces the size and weight of the autoclave, reducing its shipping costs much more than the cost of shipping the door and hinge assembly, whether assembled together or shipped as two separate parts. Alternatively, the door may be welded to the hinge assembly and shipped as one part, the hinge assembly and door being readily assembled to the autoclave body at the destination by bolting the two parts together.

Abstract: A Waste Material Sterilizing and Size Reduction Apparatus A waste treatment apparatus and a method of treating waste using such an apparatus is described. The apparatus comprises a sealable vessel with an auger mounted therein. The vessel is adapted to receive the waste, and is then sealed. The application of steam to the waste which is rotated within the vessel using the auger effects a sterilizing of the waste material.

Abstract: A method of impregnating a polymeric medical device with an antimicrobial agent is disclosed. The method involves forming a solution by dissolving triclosan in a compressed fluid and contacting the polymeric medical device with the solution. After the solution has been infused into the polymeric medical device, the solution and the medical device are separated.

Abstract: An enclosure assembly (10, 10, 10) includes a framework (12) formed from structural members and a flexible transparent enclosure (14) which provides an enclosed space for isolation and or treatment of patients, equipment, and the like. A treatment material, such as hydrogen peroxide or other gaseous or vapor sterilant, may be fed to the enclosure to microbially decontaminate or otherwise treat the equipment. The enclosure is quickly assembled and disassembled after use, making it suitable for treatment of large pieces of equipment which are not readily moved or which are too large to be accommodated conventional sterilization equipment.

Abstract: The invention relates to a device for carrying out the process, which enables the disinfection of flat and enclosing surfaces using steam. In order to achieve this, a disinfection head 1, which exhibits a nozzle assembly 3 and a suction bell 6, is connected to a holder 2 such that it can move. The holder has an inlet hose 13 to enable the steam to be introduced into the disinfection head and an outlet suction hose 7. The inlet hose is connected to an initial evaporator cell 9 and the outlet suction hose is connected to a collection container 8. The initial evaporator cell, the collection is container, the suction pumps and the necessary valves and heating elements are joined together in a mobile unit 23.

Abstract: Pressurized web treatment systems include a moving web that passes through a pressurized treatment chamber having a sealing assembly with a leakage control system. Leakage control is achieved by the cooperative effect of localized leak detectors and leak reduction means that applies a local sealing force on the seal assembly responsive to a signal from the leak detectors such that increased sealing occurs in the vicinity of the leak. In particular, an air press for paper web dewatering has improved efficiency by virtue of the leakage control system, which features local leak detectors and local force generation means associated with a flexible seal assembly to reduce leakage at the edges of the stationary plenum of the air press. Local leak detection can be based on sonic measurement with microphones, detection of escaping tracer gas, optical signals, and other means.

Abstract: Methods and apparatus in which pressure provides precise control over the timing and preferably synchronization of chemical reactions, particularly enzymatic reactions.

Abstract: A sterilizing apparatus and method in which a sanitizing device detects pressure of steam rather than temperature. The pressure is related to a desired temperature, but detection of pressure means that temperature sensors do not need to be exposed to the steam. In addition, the steam can be fully saturated, and sterilization can be obtained without the need for a drying cycle. The liquid does not need to be reused in the apparatus, ensuring that biofilm contamination of articles can be substantially reduced.

Abstract: Ultraviolet radiation is used to disinfect air (105) in a flow tube (110), where the flow tube (110) includes total internal reflecting features (120) on a portion of its external surface and said ultraviolet radiation propagates through a portion of the flow tube via total internal reflection.

Abstract: Apparatus and methods are disclosed for decontaminating mail. The preferred embodiment includes a sealable container of sufficient size to hold one or more pieces of mail. A chamber, in gaseous communication with the container, holds a quantity of oxidizer material, and a heater is used to raise the temperature of the oxidizer to form a disinfecting gas that permeates the mail. The oxidizer material is preferably a liquid such as chlorine dioxide or hydrogen peroxide. The apparatus may further include a timer so that the oxidizer is heated for a desired period of time, a pressure relief valve, and/or an indicator responsive to the pressure within the container when sealed.

Abstract: Disclosed are a pressure heating method and a pressure heating apparatus which can prevent deformation of articles or deterioration of the quality of the articles due to supply of excessive pressure and heat. After performing pressurizing and heating processing of articles by supplying steam to a pressure vessel, the supply of steam is stopped and air is supplied to the pressure vessel to keep the internal pressure of the pressure vessel within the range not exceeding the maximum value of the internal pressure at the time of pressurizing and heating. A cooling water spray device on a circulation pipe is operated along with a turbo blower so as to condense it for gradual removal. After completing the removal of the steam, the articles are cooled by the operation of the cooling water jet unit. By avoiding an abrupt decrease in the pressure inside the pressure vessel through preventing an instant condensation of the whole steam, an excessive pre-load becomes unnecessary at the final stage of sterilization.

Abstract: Installation for the drying, heating, sterilization or disinfection of dry, moist or wet materials or materials in a moist environment and of liquids, particularly waste which may be infected, e.g., medical waste, in which the materials to be treated are introduced into a microwave-permeable vessel in a pressure-proof treatment space which can be acted upon by microwaves and sealed in a pressure-tight manner, wherein a plurality of magnetrons are coupled into the resonant space forming the treatment space in such a way that microwave dead spaces are prevented, wherein the physical parameters in the device are monitored and utilized for controlling the installation, and wherein added units are also provided for influencing the course of the process.

Abstract: The invention relates to an autoclave for medical appliances and instruments with a chamber (13) in which the appliances to be sterilized are located, with a steam generator (5) and a condensate collector (11), whereby the steam generator is connected with the chamber (13) by a steam pipe (9) and the condensate collector (11) is connected with the chamber (13) by a feed pipe (35) of the condensate.

Abstract: A product carrier for use in pressure processing substances is substantially fluidically closed, and is insulated, to prevent heat transfer from the product being treated to the cooler wall of the pressure vessel. The insulating material has compression heating properties, such that as the product is pressurized, the temperature of the insulation increases as does the temperature of the product and pressure media, thereby helping to prevent heat transfer from the product to the surrounding media and pressure vessel wall.

Abstract: A method for treating the liquid phase of contaminated materials that are disinfected or sterilized in a treatment chamber is provided, whereby a defined liquid collector area is provided in the treatment chamber. When the liquid in the collector area reaches a maximum level it is discharged into a collector tank and when the level of liquid in the collector area reaches a minimum level liquid is returned to the treatment chamber. When the liquid in the collector tank reaches a maximum level, liquid therefrom is returned to the treatment chamber in case the maximum level of liquid in the treatment chamber is not reached or said liquid is treated in an additional high-temperature disinfector unit to obtain purified liquid. A device that carries out the method is also provided. Using the method or device provided, contaminated solid materials with a high proportion of liquid can be disinfected or sterilized.

Abstract: The invention relates to a high-pressure device (1) having a cylindrical high-pressure vessel (3) and prestressing means in order to exert an axial pressure on the vessel. The vessel (3) can have been formed from a number of layers of composite material, such as glass, carbon or aramide fibers which are oriented in the peripheral direction and are embedded in a matrix of epoxy resin or polyurethane. By applying the axial prestress to the pressure vessel (3), the tangential stress is distributed more uniformly over the wall thickness of the high-pressure vessel (3), the stress decreasing at the inside of the wall and increasing at the outside thereof. As a result, the innermost fibers of a high-pressure vessel (3) made of composite material are subjected to appreciably less stress, which has a beneficial effect on the life of the high-pressure vessel (3), and all fibers of the wall are utilized effectively.