Abstract: A device mount for a mobile device includes an integrated power delivery management assembly that provides a convenient and versatile solution for connection between the mobile device and an external device, where the external device may or may not be compatible with USB Type-C Power Delivery protocols. The power delivery management assembly determines, by a power delivery detect circuit, a power delivery status of the external device and configures itself accordingly. When the external device is Power Delivery incapable, the power delivery management assembly facilitates USB Type-C Power Delivery protocol between the external device and the mobile device on behalf of the external device. When the external device is Power Delivery capable, the power delivery management assembly configures itself into a “pass-through” mode to allow the external device and the mobile device to negotiate USB Type-C Power Delivery.

Abstract: A gas filter device for a medical device that provides a gas to a patient including first and second gas filter elements; a body defining a cavity receives the first and second gas filter elements in series and spaced apart from, each other; first and second end walls at opposites ends of the cavity; a first coupler extending from the first end wall; a second coupler extending from the second end wall, wherein the first coupler and the second coupler define a flow channel in communication with the cavity.

Abstract: Cosmetic formulations and compositions customized and/or personalized for rejuvenation of skin and/or hair are described. The cosmetic formulations are customized and/or personalized to include an extract and/or one or more molecular components in amounts and ratios naturally produced by rejuvenated cells or by cells modified toward rejuvenation. These cells are of skin and/or hair origin that have been reprogrammed, in which the skin and/or hair cells, having been rejuvenated and/or modified from the original cell, are initially obtained from a subject for which a customized cosmetic composition is for, or from a subject representative of a person for which a customized cosmetic composition is for.

Abstract: Cosmetic formulations and compositions customized and/or personalized for rejuvenation of skin and/or hair are described. The cosmetic formulations are customized and/or personalized to include an extract and/or one or more molecular components in amounts and ratios naturally produced by rejuvenated cells or by cells modified toward rejuvenation. These cells are of skin and/or hair origin that have been reprogrammed, in which the skin and/or hair cells, having been rejuvenated and/or modified from the original cell, are initially obtained from a subject for which a customized cosmetic composition is for, or from a subject representative of a person for which a customized cosmetic composition is for.

Abstract: Cosmetic formulations and compositions customized and/or personalized for rejuvenation of skin and/or hair are described. The cosmetic formulations are customized and/or personalized to include an extract and/or one or more molecular components in amounts and ratios naturally produced by rejuvenated cells or by cells modified toward rejuvenation. These cells are of skin and/or hair origin that have been reprogrammed, in which the skin and/or hair cells, having been rejuvenated and/or modified from the original cell, are initially obtained from a subject for which a customized cosmetic composition is for, or from a subject representative of a person for which a customized cosmetic composition is for.

Abstract: A gas filter device for a medical device that provides a gas to a patient including first and second gas filter elements; a body defining a cavity receives the first and second gas filter elements in series and spaced apart from, each other; first and second end walls at opposites ends of the cavity; a first coupler extending from the first end wall; a second coupler extending from the second end wall, wherein the first coupler and the second coupler define a flow channel in communication with the cavity.

Abstract: A single use injector is a disposable injection device that is specifically optimized for production using the blow fill seal (BFS) manufacturing process and includes various mechanisms that render the device inoperable and facilitate its safe disposal after use. The single use injector incorporates an ampoule aseptically filled with a medication that is coupled to a hermetically sealed component system. The hermetically sealed component system incorporates various mechanisms that are actuated during the use of the injection device. The injection device is encased in a removable overtube that prevents contamination. upon removal of the overtube, the injection device is activated, by compression of a needle cap that irreversible punctures the ampoule in order to inject the medication through a needle. The injection device additionally incorporates a shield that deploys over the needle following injection of the medication into a patient.

Abstract: A single use injector is a disposable injection device that is specifically optimized for production using the blow fill seal (BFS) manufacturing process and includes various mechanisms that render the device inoperable and facilitate its safe disposal after use. The single use injector incorporates an ampoule aseptically filled with a medication that is coupled to a hermetically sealed component system. The hermetically sealed component system incorporates various mechanisms that are actuated during the use of the injection device. The injection device is encased in a removable overtube that prevents contamination. upon removal of the overtube, the injection device is activated, by compression of a needle cap that irreversible punctures the ampoule in order to inject the medication through a needle. The injection device additionally incorporates a shield that deploys over the needle following injection of the medication into a patient.

Abstract: A single use injector is a disposable injection device that is specifically optimized for production using the blow fill seal (BFS) manufacturing process and includes various mechanisms that render the device inoperable and facilitate its safe disposal after use. The single use injector incorporates an ampoule aseptically filled with a medication that is coupled to a hermetically sealed component system. The hermetically sealed component system incorporates various mechanisms that are actuated during the use of the injection device. The injection device is encased in a removable overtube that prevents contamination. upon removal of the overtube, the injection device is activated, by compression of a needle cap that irreversible punctures the ampoule in order to inject the medication through a needle. The injection device additionally incorporates a shield that deploys over the needle following injection of the medication into a patient.

Abstract: Cosmetic formulations and compositions customized and/or personalized for rejuvenation of skin and/or hair are described. The cosmetic formulations are customized and/or personalized to include an extract and/or one or more molecular components in amounts and ratios naturally produced by rejuvenated cells or by cells modified toward rejuvenation. These cells are of skin and/or hair origin that have been reprogrammed, in which the skin and/or hair cells, having been rejuvenated and/or modified from the original cell, are initially obtained from a subject for which a customized cosmetic composition is for, or from a subject representative of a person for which a customized cosmetic composition is for.

Abstract: A prefilled medical injection device with production specific elements is provided as a single use disposable injection device that is optimally suited for mass production through the Blow Fill Seal manufacturing process. The device utilizes a valve and a needle assembly fused to an insert. The valve and the needle assembly are positioned within the insert forming a conduit. The needle assembly is covered with a needle cap that is detachably coupled to protecting the needle assembly from contamination and a user from accidental needle stick. The insert is engaged to the bellows during the BFS manufacturing process and hermetically sealed by a paris on layer that covers exterior portion of the insert and the needle cap. The parison layer is formed and trimmed creating exterior features that facilitate the use of the prefilled medical injection.

Abstract: Devices and systems for vehicle monitoring, safety, and tracking are disclosed. Devices related to the present disclosure have a housing having at least one actuator, two or more flexible arms having attached video cameras, a processor positioned within the housing, the processor in electronic communication with each of the video cameras, a GPS receiver, and an accelerometer. The device can transmit and receive data wirelessly through a transceiver. A central server may be associated with one or more of the devices and allow users to track vehicle status remotely.

Abstract: A prefilled medical injection device with production specific elements is provided as a single use disposable injection device that is optimally suited for mass production through the Blow Fill Seal manufacturing process. The device utilizes a valve and a needle assembly fused to an insert. The valve and the needle assembly are positioned within the insert forming a conduit. The needle assembly is covered with a needle cap that is detachably coupled to protecting the needle assembly from contamination and a user from accidental needle stick. The insert is engaged to the bellows during the BFS manufacturing process and hermetically sealed by a parison layer that covers exterior portion of the insert and the needle cap. The parison layer is formed and trimmed creating exterior features that facilitate the use of the prefilled medical injection.

Abstract: A single use injector is a disposable injection device that is specifically optimized for production using the blow fill seal (BFS) manufacturing process and includes various mechanisms that render the device inoperable and facilitate its safe disposal after use. The single use injector incorporates an ampoule aseptically filled with a medication that is coupled to a hermetically sealed component system. The hermetically sealed component system incorporates various mechanisms that are actuated during the use of the injection device. The injection device is encased in a removable overtube that prevents contamination. upon removal of the overtube, the injection device is activated, by compression of a needle cap that irreversible punctures the ampoule in order to inject the medication through a needle. The injection device additionally incorporates a shield that deploys over the needle following injection of the medication into a patient.

Abstract: A prefilled medical injection device with production specific elements is provided as a single use disposable injection device that is optimally suited for mass production through the Blow Fill Seal manufacturing process. The device utilizes a valve and a needle assembly fused to an insert. The valve and the needle assembly are positioned within the insert forming a conduit. The needle assembly is covered with a needle cap that is detachably coupled to protecting the needle assembly from contamination and a user from accidental needle stick. The insert is engaged to the bellows during the BFS manufacturing process and hermetically sealed by a parison layer that covers exterior portion of the insert and the needle cap. The parison layer is formed and trimmed creating exterior features that facilitate the use of the prefilled medical injection.

Abstract: A removable collar of flexible, absorbent material fits over the neck of a bottle. The collar absorbs liquids that drip from the bottle. The material is initially shaped as an isosceles trapezoid. The collar is formed into a truncated, generally conical shape by overlapping two opposing vertices at each end of the shorter parallel edge of the trapezoid to form a point at a lower end of the collar to produce the appearance of a “cravat.” A vertex at the longer edge of the trapezoid overlaps a portion of the shorter edge of the trapezoid and is secured to the overlapped portion at a single point. The generally conical collar has an upper opening that expands to allow the collar to pass around the enlarged flange near the top of the bottle. The upper opening snaps back to an original size to fit against the neck of the bottle.

Abstract: Methods and associated structures for limiting the number of sessions presently active between a server process and client processes distributed over a number of computing devices on a network. The methods and associated structures serve to reduce resource hogging by a particular computing device on a network and thereby reduce opportunities for denial of service attacks on the security of a server node. The server process maintains a session log to record each presently active session between the server process and a computing node identified by a source identifier provided by the client with the establishment and termination of each session. When the number of such active sessions for a particular source identity exceeds the predetermined threshold further requests to establish new sessions associated with that same source identity are rejected by the server process.

Abstract: Methods and associated structure for allocating computing resources among the plurality of cgi-bin processes spawned by a Web server process such that high-priority customers receive priority in allocation of such computing resources for cgi-bin processes its bond on behalf of high-priority customers. The methods and structures of the present invention preferably utilize Hewlett-Packard's process resource monitor (“PRM”) scheduling features to define customer relationship levels as a parameter in the allocation of computing resources. Customer or user ID information associated with a requesting Web client process are associated with the process on behalf of the requesting client. PRM configuration information then mapped such user or customer ID information to a particular priority level for allocation of computing resources.

Abstract: A method, system and article for optimizing the processing of switch transactions and updating multiple switches of a communications network based on a single transaction is provided. When a switch is backlogged with transactions beyond a threshold quantity, those transactions heading to the backlogged switch are grouped together, placed in a file and sent to the switch as a single transaction. Some of the batched individual transactions may be dependent upon other switches as well. The present invention accommodates for multiple dependencies and responds with a success notification only when all portions of the original transaction are complete. In another aspect of the invention, where multiple switches require updating, such updating can be accomplished with only a single transaction. Switch identification information is included with the transaction permitting multiple switches to be updated from the single transaction.

Abstract: The invention provides a system and method for communicating to a customer device. Briefly described, one embodiment is an access portal configured to relay communications between a customer device and a server device comprising a first access port coupled to a communication system and configured to receive a first communication directed to the access portal from the customer device, the first communication identifying the access portal with an access portal identifier and further requesting content from the server device; a processor configured to map a server device identifier to the received first communication, the server device identifier identifying the server device; and a second access port configured to transmit the first communication with the mapped server device identifier onto a high quality of service communication system such that the first communication is directed to the server device coupled to the high quality of service communication system.