Abstract: A needle shield removal assembly includes a needle shield gripper configured to operatively engage a needle shield, and a gripper holder, wherein the needle shield gripper is secured to the gripper holder via a connection interface, wherein the connection interface is formed by a holder interface feature engaging a gripper interface feature, wherein the gripper holder has an opening configured to receive the needle shield gripper and/or the needle shield, wherein the holder interface feature is offset from the opening, wherein the gripper holder defines a receiving space within which the needle shield gripper is received, wherein the receiving space has an axial extension, and wherein the needle shield gripper and the gripper holder are adjusted to one another to reduce mechanical contact of a) the gripper holder and a bent region of the needle shield gripper and/or b) the gripper holder and an edge of the needle shield gripper.

Abstract: A drug delivery device is proposed which comprises: a housing defining an interior; a reservoir which is adapted to contain a drug or contains a drug, the reservoir being retained in the interior; and a closure part which is secured relative to the housing and has to be disconnected from the housing to get access to the reservoir within the interior, wherein the closure part is secured relative to the housing by a connection, wherein the connection comprises a welded connection, and wherein the welded connection is formed between two join partners, i.e. a first join partner and a second join partner. Further, a method for manufacturing a drug delivery device is disclosed as is a use associated with drug delivery devices.

Abstract: A drug delivery device comprises a housing and a mechanical assembly, which is at least partially accommodated in the housing. The mechanical assembly comprises a predetermined breaking member, which is configured to be damaged when forcefully separated from the housing.

Abstract: A drug delivery device (1) is provided comprising a housing (2), a cartridge holder (3) which is adapted and arranged for receiving a cartridge (4) for holding a plurality of doses of a drug (5), wherein the cartridge holder (3) is removable from the housing (2) to enable an exchange of the cartridge (4), a piston rod (9) adapted and arranged to be moved from an initial position towards an end position for dispensing a dose of drug (5) from the device (1) and to be moved from the end position back towards the initial position to perform a reset operation of the device (1), and at least one resilient member (20, 25). The at least one resilient member (20, 25) is in direct mechanical contact with the piston rod (9) and the resilient member (20, 25) is adapted and arranged to prevent an unintentional movement of the piston rod (9) towards the initial position due to mechanical cooperation with the piston rod (9).

Abstract: A drug delivery device comprises a housing and a mechanical assembly, which is at least partially accommodated in the housing. The mechanical assembly comprises a predetermined breaking member, which is configured to be damaged when forcefully separated from the housing.

Abstract: A drug delivery device (1) is provided comprising a housing (2), a cartridge holder (3) which is adapted and arranged for receiving a cartridge (4) for holding a plurality of doses of a drug (5), wherein the cartridge holder (3) is removable from the housing (2) to enable an exchange of the cartridge (4), a piston rod (9) adapted and arranged to be moved from an initial position towards an end position for dispensing a dose of drug (5) from the device (1) and to be moved from the end position back towards the initial position to perform a reset operation of the device (1), and at least one resilient member (20, 25). The at least one resilient member (20, 25) is in direct mechanical contact with the piston rod (9) and the resilient member (20, 25) is adapted and arranged to prevent an unintentional movement of the piston rod (9) towards the initial position due to mechanical cooperation with the piston rod (9).

Abstract: A drive assembly for a medication delivery device is provided, comprising a piston rod which is movable from a start position to an end position for medication delivery and resettable from the end position to the start position. The drive assembly further comprises a guide member, being in engagement with the piston rod, and an impeding element for impeding a movement of the guide member during a reset of the piston rod and thereby impeding the reset of the piston rod. Furthermore, a medication delivery device comprising the drive assembly is disclosed.

Abstract: A drive assembly for a drug delivery device is disclosed. The drive assembly is connectable with a cartridge holder and comprises a housing, a piston rod, the piston rod being movable in a distal direction for drug delivery, and a guide nut, the guide nut being rotatable relative to the housing around an axis of the assembly and provided for guiding the piston rod. A locking means is provided which is enabled to take an engaged state in which the locking means is engaged with the guide nut in order to prevent rotation of the guide nut and to take a disengaged state in which the locking means is disengaged from the guide nut in order to allow rotation of the guide nut. Moreover, a coupling means is provided, the coupling means being rotatable relative to the housing around the axis of the assembly for interaction with the locking means in order to change between the engaged state and the disengaged state of the locking means.

Abstract: A method for analyzing formation fluid in a subterranean formation is disclosed, wherein the method includes the steps of: adding a scavenger compound to an analytical reagent to form a reagent solution; collecting an amount of formation fluid into a formation tester, wherein the formation tester includes at least one fluids analyzer comprising at least one probe, at least one flow line, at least one reagent container, and at least one spectral analyzer, wherein the fluids analyzer is configured such that the collected formation fluid is fed through the at least one flow line to the at least one spectral analyzer; mixing an amount of the collected formation fluid with an amount of the reagent solution to form a mixture; and analyzing the mixture downhole.

Abstract: Methods and related apparatuses and mixtures are described for spectroscopic detection of hydrogen sulfide in a fluid, for example a formation fluid downhole. A reagent mixture is combined with the fluid. The reagent mixture includes metal ions for reacting with hydrogen sulfide forming a metal sulfide, and a capping agent that limits growth of the insoluble metal sulfide species by electrosteric or steric stabilization. The particle growth is one of chemical reaction or significant aggregation, and the capping agent further functionalizes the reagent mixture to exhibit properties outside the natural characteristics of the metal sulfide species to allow for spectroscopic detection of the metal sulfide species. The combined mixture and fluid is then spectroscopically interrogated to detect the presence of the metal sulfide thereby indicating the presence of hydrogen sulfide in the fluid. The mixture also includes chelating ligands for sustaining thermal endurance of the mixture under downhole conditions.

Abstract: A drive assembly for a medication delivery device is provided, comprising a piston rod which is movable from a start position to an end position for medication delivery and resettable from the end position to the start position. The drive assembly further comprises a guide member, being in engagement with the piston rod, and an impeding element for impeding a movement of the guide member during a reset of the piston rod and thereby impeding the reset of the piston rod. Furthermore, a medication delivery device comprising the drive assembly is disclosed.

Abstract: A drive assembly for a drug delivery device is disclosed. The drive assembly is connectable with a cartridge holder and comprises a housing, a piston rod, the piston rod being movable in a distal direction for drug delivery, and a guide nut, the guide nut being rotatable relative to the housing around an axis of the assembly and provided for guiding the piston rod. A locking means is provided which is enabled to take an engaged state in which the locking means is engaged with the guide nut in order to prevent rotation of the guide nut and to take a disengaged state in which the locking means is disengaged from the guide nut in order to allow rotation of the guide nut. Moreover, a coupling means is provided, the coupling means being rotatable relative to the housing around the axis of the assembly for interaction with the locking means in order to change between the engaged state and the disengaged state of the locking means.

Abstract: Methods and related apparatuses and mixtures are described for spectroscopic detection of hydrogen sulfide in a fluid, for example a formation fluid downhole. A reagent mixture is combined with the fluid. The reagent mixture includes metal ions for reacting with hydrogen sulfide forming a metal sulfide, and a capping agent that limits growth of the insoluble metal sulfide species by electrosteric or steric stabilization. The particle growth is one of chemical reaction or significant aggregation, and the capping agent further functionalizes the reagent mixture to exhibit properties outside the natural characteristics of the metal sulfide species to allow for spectroscopic detection of the metal sulfide species. The combined mixture and fluid is then spectroscopically interrogated to detect the presence of the metal sulfide thereby indicating the presence of hydrogen sulfide in the fluid. The mixture also includes chelating ligands for sustaining thermal endurance of the mixture under downhole conditions.

Abstract: A method for analyzing formation fluid in a subterranean formation is disclosed, wherein the method includes the steps of: adding a scavenger compound to an analytical reagent to form a reagent solution; collecting an amount of formation fluid into a formation tester, wherein the formation tester includes at least one fluids analyzer comprising at least one probe, at least one flow line, at least one reagent container, and at least one spectral analyzer, wherein the fluids analyzer is configured such that the collected formation fluid is fed through the at least one flow line to the at least one spectral analyzer; mixing an amount of the collected formation fluid with an amount of the reagent solution to form a mixture; and analyzing the mixture downhole.

Abstract: A linearized thermal and optical model of an optical integrated circuit can be used to temperature-stabilize one or more optical elements of the circuit using active temperature regulation. To stabilize a single optical element, a temperature sensor and a heater can be provided proximate to the grating. Thermal and optical coefficients can be then used to select an appropriate temperature set-point for the temperature controller that receives readings from the sensor and determines the power dissipated in the heater. Multiple optical elements can be stabilized individually, using the same process and lumping cross-heating factors together with other environmental factors. Alternatively, multiple AWG's can be stabilized using fewer sensors than optical elements, by stabilizing one of the optical elements in the same manner as in the case of a single optical elements, and determining power dissipated in the heaters of the remaining optical elements based on the linearized model.

Abstract: A linearized thermal and optical model of an optical integrated circuit can be used to temperature-stabilize one or more optical elements of the circuit using active temperature regulation. To stabilize a single optical element, a temperature sensor and a heater can be provided proximate to the grating. Thermal and optical coefficients can be then used to select an appropriate temperature set-point for the temperature controller that receives readings from the sensor and determines the power dissipated in the heater. Multiple optical elements can be stabilized individually, using the same process and lumping cross-heating factors together with other environmental factors. Alternatively, multiple AWG's can be stabilized using fewer sensors than optical elements, by stabilizing one of the optical elements in the same manner as in the case of a single optical elements, and determining power dissipated in the heaters of the remaining optical elements based on the linearized model.

Abstract: A linearized thermal and optical model of an optical integrated circuit can be used to temperature-stabilize one or more optical elements of the circuit using active temperature regulation. To stabilize a single optical element, such as an arrayed waveguide grating (AWG), a temperature sensor and a heater can be provided proximate to the grating. Thermal and optical coefficients can be then used to select an appropriate temperature set-point for the temperature controller that receives readings from the sensor and determines the power dissipated in the heater. Multiple AWG's can be stabilized individually, using the same process and lumping cross-heating factors together with other environmental factors. Alternatively, multiple AWG's can be stabilized using fewer sensors than AWG's, by stabilizing one of the AWG's in the same manner as in the case of a single AWG, and determining power dissipated in the heaters of the remaining AWG's based on the linearized model.

Abstract: A linearized thermal and optical model of an optical integrated circuit can be used to temperature-stabilize one or more optical elements of the circuit using active temperature regulation. To stabilize a single optical element, such as an arrayed waveguide grating (AWG), a temperature sensor and a heater can be provided proximate to the grating. Thermal and optical coefficients can be then used to select an appropriate temperature set-point for the temperature controller that receives readings from the sensor and determines the power dissipated in the heater. Multiple AWG's can be stabilized individually, using the same process and lumping cross-heating factors together with other environmental factors. Alternatively, multiple AWG's can be stabilized using fewer sensors than AWG's, by stabilizing one of the AWG's in the same manner as in the case of a single AWG, and determining power dissipated in the heaters of the remaining AWG's based on the linearized model.

Abstract: The invention relates to an optical device which carries multiple optical signals where the optical device has a plurality of distal waveguides some of which may be configured to control insertion loss among the multiple optical signals.

Abstract: An optical integrated circuit (OIC) or optical apparatus upon which a waveguide-grating router (WGR) device is fashioned is provided, where the circuit is configured to optimize a passband for each channel transmitted on an output waveguide. The WGR has two or more waveguides of varying widths optically coupled to a slab waveguide. The widths can be configured to facilitate producing a substantially uniform frequency-limited bandwidth, a substantially uniform wavelength-limited bandwidth, a substantially uniform isolation value, and/or a substantially uniform value for insertion loss between the output waveguides, which in turn facilitates producing optical data communication devices with more consistent transmission parameters and higher quality. In addition to various widths, the shape of the delivering end of a slab waveguide can be fashioned to further improve the consistency and quality of such parameters.