93results about How to "Easy to decompress" patented technology

A service module incorporated within the network infrastructure intercepts packets communicated between a client and a server to determine whether the connection corresponds to an email service. If so, the service module breaks the connection by terminating the connection with the client at the service module and opening a separate connection between the service module and the server. Packets communicated between the client and the server may then be redirected to an email compression application that monitors messages communicated between the client and the server and processes the messages in accordance with the state of the email session. For messages corresponding to connection establishment, user authentication and other protocol-specific messages, for example, the email compression application may be configured to forward the messages to the originally intended destination. Messages corresponding to an email message data, however, are buffered within the email compression application. Once the entire message has been received, the email compression application may strip the message headers and any protocol-specific data, compress the data and attach new message headers corresponding to the compressed email message. The compressed and reformatted email message is then reinserted into the data stream for transmission to the intended destination. Because compression may occur between the server and client, compression may be performed without requiring special processing by the server before email messages are sent. Furthermore, because the email messages may be compressed in a format that can be readily decompressed using decompression libraries incorporated within the operating system of client devices, such as the CAB format or GZIP format, the client may decompress received email messages utilizing software already incorporated within the operating system of the client device, without requiring download or installation of special decompression software and / or coordination of compression / decompression of email messages with the server or sending party.

The present invention is directed to an expandable spinal fusion intervertebral implant that provides for maintaining and creating lordosis in the human spine that can be filled with biologics while in situ to encourage spinal fusion. A threaded rod that traverses an insertion / injection handle can be rotated to operate a screw within the interbody cage that displaces opposing vertical tapped sliding wedges, causing them to converge towards each other. Such contact causes the operation of a horizontal wedge that acts as a lift to expand the interbody cage to one of various dimensions in a preferred range. At its desired expansion, the spinal fusion implant of the present invention is sized to fit within the disc space between two vertebral bodies and fill all voids left while the vertical and horizontal wedges operate within, due to the biologics being contained within the interbody cage.

A video compression system is disclosed that is optimized to take advantage of the types of redundancies typically occurring on computer screens and the types of video loss acceptable to real time interactive computer users. It automatically adapts to a wide variety of changing network bandwidth conditions and can accommodate any video resolution and an unlimited number of colors. The disclosed video compression encoder can be implemented with either hardware or software and it compresses the source video into a series of data packets that are a fixed length of 8 bits or more. Sequences of one or more of these packets create unique encoding “commands” that can be sent over any network and easily decoded (decompressed) with either software or hardware. The commands include 3 dimensional copying (horizontal, vertical and time) and unique efficiencies for screen segments that are comprised of only two colors (such as text). Embodiments are also disclosed that improve the video compression depending on the popularity of pixel colors.

A spring retainer (60) for a syringe (10) that has a barrel (40), a plunger (20), a spring (90) and a retractable needle (50) that can couple with the plunger for spring-driven retraction of the coupled needle and plunger. The spring retainer has first (70) and second (80) body members that cooperate to releasably maintain the spring in a compressed state until the plunger is coupled to the retractable needle after depression of the plunger to deliver the fluid contents of the syringe. Depression of the plunger triggers rotational disengagement of the first and second body members to allow decompression of the spring which forces retraction of the needle into the barrel. Rotational disengagement of the first and second body members also assists rotation of the plunger into a final, inoperable position.

A spring retainer (60) for a syringe (10) that has a barrel (40), a plunger (20), a spring (90) and a retractable needle (50) that can couple with the plunger for spring-driven retraction of the coupled needle and plunger. The spring retainer has first (70) and second (80) body members that cooperate to releasably maintain the spring in a compressed state until the plunger is coupled to the retractable needle after depression of the plunger to deliver the fluid contents of the syringe. Depression of the plunger triggers rotational disengagement of the first and second body members to allow decompression of the spring which forces retraction of the needle into the barrel. Rotational disengagement of the first and second body members also assists rotation of the plunger into a final, inoperable position.

A retractable syringe (10) and plunger (20) therefore are provided, the syringe having a barrel (20), a retractable needle mount (40) to which is mounted or is mountable a needle (11), and a plunger (80), the plunger comprising an initially compressed spring (60), a means for engaging the retractable needle mount, an integrally formed plunger seal (22) and a removable controlling means (70) for facilitating control of the rate of retraction of needle mount when engaged with plunger. The needle mount is held in the barrel by a holding means which prevents inadvertent retraction of the needle mount when the plunger is withdrawn to fill the syringe. The holding means comprises a plurality of clips (196A, 196B, 196C) that may be integrally formed with the barrel or may be present on a cap mounted to the barrel. An ejector means (52) is also provided, whereby plunger depression can urge the ejector means to release the needle from the holding means and thereby allow retraction of the needle mount following decompression of the spring.

A pressure exchanger for transferring pressure energy from a relatively high-pressure fluid stream to another relatively low-pressure fluid stream is provided. A ducted rotor is positioned on a central axle between two end covers inside a pressure vessel with a coaxial inlet and outlet pair that is in communication with a pair of low pressure ports having inclination forming an inlet tangential velocity vector in the direction of rotor rotation and an outlet tangential velocity vector in opposite direction imparting a rotational momentum on rotor. A pair of high-pressure ports is adapted for flow without inclination and imparts no momentum to rotor and flow can be varied without impacting the rotor's RPM. The end covers have a sloped surface following a flat sealing area that increases the clearance in the direction of rotation causing increased outflow during depressurization and lower duct pressure before duct is exposed to low pressure port and furthermore causing increased inflow during the pressurization phase before duct is exposed to the high pressure port, which will dissipate pressure energy as opposed to producing cavitation or pressure waves with result wear and noise.

The present invention is directed to an expandable spinal fusion intervertebral implant and a method for surgically implanting said implant that provides for maintaining and creating lordosis in the human spine that can be filled with biologics while in situ to encourage spinal fusion. A threaded rod that traverses an insertion / injection handle can be rotated to operate a screw within the interbody cage that displaces opposing vertical tapped sliding wedges, causing them to converge towards each other. Such contact causes the operation of a horizontal wedge that acts as a lift to expand the interbody cage to one of various dimensions in a preferred range. In its expanded height, the overall length of the interbody cage is maintained. At its desired expansion, the spinal fusion implant of the present invention is sized to fit within the disc space between two vertebral bodies and fill all voids left while the vertical and horizontal wedges operate within, due to the biologics being contained within the interbody cage.

A retractable syringe (10) and plunger (20) therefore are provided, the syringe having a barrel (20), a retractable needle mount (40) to which is mounted or is mountable a needle (11), and a plunger (80), the plunger comprising an initially compressed spring (60), a means for engaging the retractable needle mount, an integrally formed plunger seal (22) and a removable controlling means (70) for facilitating control of the rate of retraction of needle mount when engaged with plunger. The needle mount is held in the barrel by a holding means which prevents inadvertent retraction of the needle mount when the plunger is withdrawn to fill the syringe. The holding means comprises a plurality of clips (196A, 196B, 196C) that may be integrally formed with the barrel or may be present on a cap mounted to the barrel. An ejector means (52) is also provided, whereby plunger depression can urge the ejector means to release the needle from the holding means and thereby allow retraction of the needle mount following decompression of the spring.

A retractable syringe includes a barrel, a collar mounted to the barrel, a retraction spring and a needle mount. The plunger includes a first plunger member and a second plunger member that are releasably coupled to initially compress the spring. The second plunger member further includes a seal to prevent fluid leakage between plunger and barrel. After depression of the plunger to deliver the syringe fluid contents, the first plunger member engages the needle mount with needle attached thereto and is rotatably uncoupled from the second plunger member to allow decompression of the retraction spring, which forces retraction of the first plunger member, needle mount and needle engaged therewith. The first plunger member and the collar include elements that co-operatively disable subsequent depression or withdrawal of the plunger. Following retraction of the first plunger member, the second plunger member and seal prevent refilling and re-use of the syringe.

A video compression system is disclosed that is optimized to take advantage of the types of redundancies typically occurring on computer screens and the types of video loss acceptable to real time interactive computer users. It automatically adapts to a wide variety of changing network bandwidth conditions and can accommodate any video resolution and an unlimited number of colors. The disclosed video compression encoder can be implemented with either hardware or software and it compresses the source video into a series of data packets that are a fixed length of 8 bits or more. Sequences of one or more of these packets create unique encoding “commands” that can be sent over any network and easily decoded (decompressed) with either software or hardware. The commands include 3 dimensional copying (horizontal, vertical and time) and unique efficiencies for screen segments that are comprised of only two colors (such as text). Embodiments are also disclosed that improve the video compression depending on the popularity of pixel colors.

The invention relates to a novel intraluminal tumor cryosurgery ablation catheter and an operation method thereof. The novel intraluminal tumor cryosurgery ablation catheter comprises a balloon, an air inlet pipeline, an air return pipeline, a vacuum pipeline, and an air inlet connector, an air return connector and a vacuum connector, which are respectively connected with near ends of the air inlet pipeline, the air return pipeline and the vacuum pipeline in seal mode, wherein the vacuum pipeline is located on the exteriors of the air inlet pipeline and the air return pipeline. The novel intraluminal tumor cryosurgery ablation catheter further comprises a buffer unit, wherein the buffer unit is arranged at the far end of the air inlet pipeline, and arranged in the balloon, the buffer unit is provided with a buffer air outlet, the near end of the buffer unit is connected with the far end of the air inlet pipeline or the air return pipeline in seal mode, the far end face of the balloon is in a concave shape, the far end of the buffer unit is connected with the far end of the balloon in seal mode, and a connection point between the far end of the buffer unit and the balloon is arranged at the middle of the concave portion of the far end of the balloon or in the far end of the balloon. The novel intraluminal tumor cryosurgery ablation catheter cooperates with an endoscope so as to adapt to complex cavity environments, and the far end of the balloon is large in contact area, and thereby guarantees a large freezing range.

Fixation devices and methods for stabilization of the lamina after laminoplasty are described. The device comprises of a plate with several holes that receive bone fasteners. The plate is curved at the ends to contour to the vertebral structure and has appendages to engage the displaced lamina in a fixed position. Alternatively, the plate has a bone fusion spacer in the middle to engage and fuse the lamina in the displaced position. Several methods of dynamically stabilizing the lamina after either the open door, double door or expansive laminoplasty technique are provided.

The invention provides an intelligent health sleep pillow. The intelligent health sleep pillow comprises a gesture detection part and an inflatable pillow part, wherein the gesture detection part comprises gesture detection sensors, and each gesture detection sensor comprises a sensor shell, a sensor circuit board arranged inside the sensor shell, and a button cell connected with the sensor circuit board; each sensor circuit board comprises a first single chip microcontroller unit MCU, a first bluetooth module connected with the input end of the first single chip microcontroller unit MCU, and a six-axis acceleration sensor connected with the input end of the first single chip microcontroller unit MCU; the inflatable pillow part comprises a pillow inner, a lifting air bag is arranged in the pillow inner, a flexible cushion plate is arranged above the lifting air bag, massage auxiliary air bags are arranged on the two sides above the flexible cushion plate, flexible massage cushion plates are arranged above the massage auxiliary air bags and the flexible cushion plate, and head massage combined air bags are arranged above the flexible massage cushion plates. The manual adjustment is not needed, the body sleep posture is intelligently identified, and the height of the pillow is automatically adjusted; and the intelligent health sleep pillow has the advantage of being accurate in detection, reliable in action, and high in intelligent degree.

A method for compressing a high dynamic range (HDR) texture. A first block of texels of the HDR texture in a red-green-blue (RGB) space may be transformed to a second block of texels in a luminance-chrominance space. The first block may have red values, green values and blue values. The second block may have luminance values and chrominance values. The chrominance values may be based on a sum of the red values, a sum of the green values and a sum of the blue values. The luminance values and the chrominance values may be converted to an 8-bit integer format. The luminance values may be modified to restore a local linearity property to the second block. The second block may be compressed.

The invention provides a pressure-stabilizing valve comprising a shell, a left end cover, a right end cover and a spool component. The shell comprises a left chamber, a right chamber and a valve hole provided between the left and right chambers; the peripheral wall of the right chamber is provided with a water inlet; the peripheral wall of the valve hole is provided with a water outlet; a junction of the right chamber and the valve hole is provided with a valve seat portion having an inner conical wall; the left end cover and the right end cover are hermetically connected to two ends of the shell, respectively; the spool component penetrates the valve hole of the shell and comprises a piston portion and a sealing portion; the piston portion is limited in the left chamber of the shell and hermetically slides in the axial direction; the sealing portion can be hermetically abutted to the inner conical wall. Through relieved changes in area of water passing between the sealing portion and the inner conical wall along with gradual increase of water pressure, the water from the water inlet to the water outlet is well pressure-relieved, pressure-stabilized and flow-stabilized, especially when a water resource is under the high pressure 50 PSI (pounds per square inch) to 100 PSI.

A kit for evacuating a collection of fluid from the subdural space of a patient is disclosed, and includes a subdural evacuating port device having a proximal end and a distal end. The subdural evacuating port device has a tubular portion with a lumen extending between the proximal and distal ends. An exterior surface of the proximal end of the tubular portion has self-tapping threads formed thereon for cutting threads into a skull. Retaining elements are located on the exterior surface of the tubular portion adjacent to the distal end for engaging an interior surface of a conduit with a flexible wall to releasably retain the conduit on the distal end of the tubular portion. A pair of wings extend outwardly from the tubular portion in opposite directions. The kit also includes elements for performing placement of the subdural evacuating port device in the patient.

A replaceable forehead liner for the continuous positive airway pressure machine, which includes a base, a support, and a locking member. The base has a plurality of flexible pads and a connecting member for bridging the flexible pads. The support has a plurality of support pillars and a support plate connecting the support pillars. The support pillars, the support plate, and the flexible pads form a hollow area, and each support pillar has a hollow hole. The hollow area and holes make the support pillars elastic and compressible. The locking member forms off the surface of the support pillars and the support plate, with the locking member being wider than the side of the hollow area. The locking member has a locking portion for engaging to the clipping portion of the CPAP mask. Functionally, the replaceable forehead liner is more secured and improves pressure relief for the user.

A novel probe design is presented that increases a probe tolerance to stress fractures. Specifically, what is disclosed are three features increase stress tolerance. These features include a various union angle interface edge shapes, pivot cutouts and buffers.

Embodiments of the invention provide an encrypted compressed file processing method and apparatus. The method comprises the steps of obtaining an original file selected by a target user; and performing encryption compression on the original file to obtain a compressed file, recording file information of the compressed file, and after triggering operation of storing the file information of the first compressed file by the target user is obtained, sending the file information of the first compressed file and a target user name to a server, thereby enabling the server to store the file information of the first compressed file in a corresponding information library according to the target user name. The storage of a password of the compressed file is finished, so that the decompression of thefile after the password is forgotten subsequently is facilitated.

The present invention combines into a single housing a multiplicity of features that may be used separately or together to facilitate stress reduction in the user. A central computer receives inputs and sends signals to facilitate activation of a visual display as well as an audio output. Several power supply options are provided. A pulse sensor may be attached to the user to sense their pulse rate. The audio input provides a soothing noise such as a beating sound, the frequency of which may be adjusted, for example, 30 to 120 beats per minute. A voice synthesizer may speak directions to the user such as, for example, instructing the user to breathe in and out at a certain rate. A timer and speed control permit ready adjustment of the frequency of beats as well as the frequency during which voice synthesizer messages are provided. A microphone and tape recorder allow the user to tape record their own stress reducing instructions. A visual display includes an arc made up of a multiplicity of LEDs and a display of the heart rate. The audio output may include a speaker and a volume control.

It consists of an equipment (1) for passive stretching of the structures of the spine; constituted by auto-portable structure (2) endowed of superior moto-reducer set (3) with pulley (4) passible of moving, upwards or downwards, an one-line connection element (5) to be fastened to a garment (V) placed in the spill of the hip of the user, with central catch (6), being such moto-reducer set (3) activated by remote control (7) and course limited by sensor (S).

An aerosol dispenser, an outer container for an aerosol dispenser and a preform for an outer container. The aerosol dispenser, outer container and preform each have a neck, which in turn has a crimp ring, to receive a valve cup clinched thereto. The crimp ring has slots which act as vents therethrough. The vents may be exposed to pressurized propellant and product due to deformation of the neck during undue internal pressurization. The cross section of the vents diverge in the downward direction to provide both flow area and for product and propellant and adequate area for the valve cup to be corrugatedly clinched to the crimp ring.

Fixation devices and methods for stabilization of the lamina after laminoplasty are described. The device comprises of a plate with several holes that receive bone fasteners. The plate is curved at the ends to contour to the vertebral structure and has appendages to engage the displaced lamina in a fixed position. Alternatively, the plate has a bone fusion spacer in the middle to engage and fuse the lamina in the displaced position. Several methods of dynamically stabilizing the lamina after either the open door, double door or expansive laminoplasty technique are provided.