Abstract: A synchronous machine (100) includes a housing, a shaft (106) to mount a three-phase rectifier (124), main motor (116) and a rotating transformer (RT) (108). The main rotor (110) is concentrically and co-axially mounted on shaft (106), and main stator (112) is concentrically and co-axially assembled over main rotor (110). Main rotor (110) includes Direct Current field windings and main stator (112) includes Alternating Current poly-phased distributed windings. Further, the RT (108) includes an RT rotor (120) and RT stator (122). RT rotor (120) and RT stator (122) may include AC poly-phase distributed windings and second predefined number of poles. Further, RT rotor (120) may be configured to be rotatably coupled on first end (106A) of shaft (106). The RT stator (122) may be configured to concentrically and co-axially assembled over RT rotor (120).

Abstract: A disinfecting cap configured to engage an open female luer connector includes a housing having an open first end, a second end, and at least one sidewall extending between the first end and the second end. The cap also includes an absorbent support or sponge disposed in the housing configured to contain a cleaning solution for cleaning and/or disinfecting portions of the open female luer connector engaged to the cap. The cap further includes a plug disposed in the housing configured to prevent ingress of the cleaning solution into a lumen in the open female luer connector.

Abstract: A device, system, and method for aseptic skin treatment and disinfection of medical connectors comprising a pad soaked with a disinfectant material, the pad having a distal face and a proximal face, a handle associated with the proximal face of the pad, the handle configured for grasping by a user to assist in manipulation of the pad for pressing and scrubbing the distal face of the pad against a surface of the skin. According to one design, an opening extends through a portion of the distal face of the pad and at least partially into a body of the pad. The opening can receive at least an end portion of the medical connector therein to disinfect the end portion of the medical connector. Alternatively the pad can be formed from a soft material capable of deforming about the end portion of the medical connector.

Abstract: A disinfecting assembly for a prefilled flushing syringe. The disinfecting assembly includes a scrubbing cap and a disinfecting cap. The scrubbing cap includes a chamber adapted to receive a needle-free connector of an intravenous (IV) catheter. A scrubber and a disinfectant are contained within the chamber of the scrubbing cap. The disinfecting cap includes a chamber adapted to receive the needle-free connector of the IV catheter. A compressible sponge and disinfectant are contained within the chamber. The disinfecting cap is removably connected to the scrubbing cap. A tip cap, adapted to connect to and cover a syringe tip of the syringe, extends from one of the disinfecting cap and the scrubbing cap or a housing connecting the disinfecting cap and the scrubbing cap. Also, a prefilled flushing syringe including the disinfecting assembly and a method of using the prefilled flushing syringe to disinfect a needle-free connector and catheter.

Abstract: A cap configured to engage connectors of different types includes a housing having a an open first end, a second end, a sidewall extending between the first end and the second end, and an opening extending through the sidewall. The cap further includes a flexible sleeve disposed in the housing having a first end, a second end, and a sleeve sidewall extending between the first end and the second end. The cap further includes: a lock connected to the housing configured to move through the opening of the housing to press against the sleeve sidewall, which causes the sleeve sidewall to directly or indirectly press against a portion of the connector to secure the connector in the housing; and an absorbent member disposed in the flexible sleeve configured to contain a cleaning solution for cleaning and/or disinfecting portions of the connector engaged to the cap.

Abstract: A cap configured to engage a male connector includes a housing having an open first end, a second end, and at least one sidewall extending between the first end and the second end. The cap also includes an outer absorbent support disposed in the housing defining a recess and a socket disposed in the recess of the outer absorbent support configured to engage the male connector for retaining the male connector within the housing. The cap also includes an inner absorbent support disposed in the socket configured to contain a cleaning solution for cleaning and/or disinfecting portions of the male connector engaged to the cap.

Abstract: A needle cover includes a needle shield, a mount coupled to the needle shield, and a disinfecting pad coupled to the mount. The disinfecting pad is fixedly coupled to the needle shield with an adhesive, and wherein the disinfecting pad is a porous material impregnated with a disinfectant. The disinfecting pad is a precut foam having a plurality of columnar structures.

Abstract: A modular medical dressing includes a layered dressing arrangement having a dressing layer with a first surface and a second surface, a release layer releasably adhered to the first surface, and a backing layer releasably adhered to the second surface. The modular medical dressing further includes a pre-defined tearable portion formed on the layered dressing arrangement. The pre-defined tearable portion is tearable from the layered dressing arrangement to reduce a surface area of the layered dressing arrangement. The pre-defined tearable portion may have a plurality of first tear lines connected to define a first tearable portion. At least a portion of the release layer is configured for use as securement tape for securing a catheter to an anatomical structure.

Abstract: Described are DNA molecules which can be transcribed into an mRNA harbouring novel UTR sequences combining the advantages of being extremely short and at the same time allowing for high translation efficiencies of RNA molecules containing them. Further, described are vectors comprising such a DNA molecule and to host cells comprising such a vector. Moreover, described are corresponding RNA molecules containing such UTRs. Further, described is a pharmaceutical composition comprising the described RNA molecule and optionally a pharmaceutically acceptable carrier as well as to the use of the described UTRs for translating a coding region of an RNA molecule into a polypeptide or a protein encoded by said coding region.

Abstract: Techniques for ripple-type control of networked physical systems such as power systems, water systems, and others are provided. As one example, a device includes at least one processor configured to determine, for a first controllable device in a system, based on a measurement of an output parameter and a minimum output parameter value, an output violation value for the first device. The processor is further configured to determine, based on a present input value for the first device, the output violation value, and an assistance requisition value corresponding to a second device, a target input value for the first device. The processor is further configured to cause the first controllable device to modify operation based on the target input value and a maximum input value for the first controllable device.

Abstract: A syringe includes a barrel having first and second ends, with the barrel defining an interior space and a stopper positioned therein, the stopper moveable within the interior space relative to the barrel, a plunger connected to the stopper, and a collar having threads configured to engage threads of a medical connector. The collar is at least partially received by the barrel, with one of the barrel and the collar defining a slot and the other of the barrel and the collar having a pin received within the slot. The collar has a connection position where the collar is fixed relative to the barrel when the syringe is being connected to the medical connector, a disconnection position where the collar is fixed relative to the barrel when the syringe is being disconnected from the medical connector, and a reuse prevention position wherein the collar is rotatable relative to the barrel.

Abstract: A skin preparation device including a body member, a fluid retention member operatively connected to a distal end of the body member, and a tip extending radially from an outer surface of the fluid retention member.

Abstract: A syringe includes a barrel having a proximal end, a distal end having a distal tip defining a channel, and a sidewall extending between the proximal end and the distal end. The syringe also includes a tip cap removably connected to the distal tip of the barrel restricting fluid flow from the channel. The tip cap includes a connector configured to receive the distal tip of the barrel forming a friction engagement with the distal tip, a cap shield connected to and extending about the connector, and a release tab extending proximally from the cap shield that secures the tip cap to the barrel. A prefilled flushing syringe including a predetermined volume of a fluid disposed within the barred of the syringe, as well as methods for expulsion of fluid from the syringe and of assembling the syringe and tip cap are also disclosed herein.

Abstract: A cap configured to engage a male connector and a female connector includes a first housing for the female connector having a closed bottom, an open top, and a sidewall extending between the bottom and the top, and a first absorbent support disposed in the first housing configured to contact portions of the female connector. The cap also includes a removable second housing for the male connector disposed in the first housing. The second housing includes a bottom, a top, and a sidewall extending between the bottom and the top with an outer surface of the sidewall of the second housing engaged to an inner surface of the sidewall of the first housing. The cap also includes a second absorbent support disposed in the removable second housing configured to contact portions of the male connector.

Abstract: A cap configured to engage different types of female connectors includes a housing having a closed bottom, an open top, and a sidewall extending between the top and the bottom with threads on an inner surface of the sidewall. The cap also includes a sleeve disposed in the housing with threads engaged to the threads of the housing configured to rotate relative to the housing, thereby moving the sleeve through the housing, and a gripper disposed at least partially in the sleeve having at least one flexible leg pressed radially inward by the sleeve as the sleeve moves through the housing. The cap also includes an absorbent support disposed in the gripper configured to clean and/or disinfect portions of the female connector.

Abstract: As described herein, a system, method, and computer program are provided for proactive 5G leg estimation. During an initial access procedure by a user equipment on a 4G leg of a 4G-LTE network, an eNodeB of the 4G-LTE network computes a parameter for the user equipment. Further, the eNodeB of the 4G-LTE network conditionally allows an addition of a 5G leg to the 4G-LTE network for the user equipment, based on the parameter computed for the user equipment.

Abstract: A system for driver risk analysis includes and/or interfaces with: a processing subsystem, a set of sensors, and a set of models and/or algorithms. Additionally or alternatively, the system can include and/or interface with any or all of: a software platform, a set of client applications, a set of user devices, and/or any other components. A method for driver risk analysis can include any or all of: collecting a set of data; analyzing the set of data to determine a set of features; analyzing the set of data to produce a set of driver risk outputs; and triggering a set of actions based on the set of driver risk outputs. Additionally or alternatively, the method can include any or all of: determining eligibility criteria associated with a set of end entities; modifying any or all of the collection of data and/or the analysis of data and/or the driver risk outputs based on the eligibility criteria; training and/or updating a set of models and/or algorithms; and/or any other processes.

Abstract: An integrated disinfection device is described syringe assembly having two integrated disinfection units assembled to a syringe for disinfecting and sterilizing corresponding medical connectors, specifically access ports of corresponding medical connectors. The integrated disinfection unit includes a first cup and a second cup. The first cup having a chamber containing a first absorbent material, a first disinfectant or an antimicrobial agent in the first cup, and a first peelable seal. The second cup having a chamber containing a second absorbent material, a second disinfectant or an antimicrobial agent in the second cup, and a second peelable seal. A threaded connection is disposed on the bottom exterior surface of the first cup having threads that are sized and pitched to engage threads of a luer lock collar on the distal end of the syringe barrel to allow the first cup to be connected to the syringe assembly.

Abstract: A syringe with an integrated vein finder is disclosed, which illuminates a potential venipuncture site of a patient and identifies a vein that is suitable for venipuncture with the syringe, for blood collection or intravenous drug administration. The syringe portion of the system includes a syringe barrel and a pointed-tip needle projecting from the distal end of the barrel for venipuncture. An illumination module is coupled to the syringe barrel; it has an illumination source that projects an electromagnetic beam into an illumination zone distal the syringe's pointed tip, for illuminating and identifying a subcutaneous vein. The integrated vein finder and syringe system is operable by a sole clinician, such as a phlebotomist, who can easily manipulate the syringe and illuminate the venipuncture site with one hand, without assistance of another clinician.

Abstract: Fluid connector systems including first and second connector portions couplable together to form a fluid pathway therethrough, and can resist fluid flow through the connector when the connector portions are separated from each other. A connector portion can include a connector housing, a luer portion, and a deformable valve member. The deformable valve member is disposed within the connector housing and includes a spherical portion extending partially through a valve opening of the connector housing. The spherical portion defines a slit, and the deformable valve member is configured to selectively prevent fluid flow from the housing volume through the valve opening and to deform to expand the slit and permit fluid flow from the housing volume through the valve opening.