Abstract: An infusion system for infusing a medication in a patient, comprising a medication dose dispensing device and a control device for controlling the dispensing device. The infusion system can be configured in a non-operating configuration, in which the dispensing device and the control device are spaced apart from each other, and in an operating configuration, in which the dispensing device and the control device are temporarily proximity-coupled. The actuating rotor of the control device and the actuated rotor of the dispensing device have a common rotation axes, and the system can compensate or block the rotation of the control device with respect to the dispensing device.

Abstract: An infusion system for infusing a medication in a patient, comprising a medication dose dispensing device and a control device for controlling the dispensing device. The infusion system can be configured in a non-operating configuration, in which the dispensing device and the control device are spaced apart from each other, and in an operating configuration, in which the dispensing device and the control device are temporarily proximity-coupled. The actuating rotor of the control device and the actuated rotor of the dispensing device have a common rotation axes, and the system can compensate or block the rotation of the control device with respect to the dispensing device.

Abstract: An infusion system for infusing a medication in a patient, comprising a medication dose dispensing device and a control device for controlling the dispensing device. The infusion system can be configured in a non-operating configuration, in which the dispensing device and the control device are spaced apart from each other, and in an operating configuration, in which the dispensing device and the control device are temporarily proximity-coupled. The actuating rotor of the control device and the actuated rotor of the dispensing device have a common rotation axes, and the system can compensate or block the rotation of the control device with respect to the dispensing device.

Abstract: A device for delivering a medical fluid (4) comprising a body which houses: at least one containment tank (20) of a medical fluid, a fluid injection device (24) which interfaces with said containment tank (20) and is suitable to allow controlled delivery of a fluid through a cannula (32), an extraction device (40) of the cannula (32) from a retracted or rest configuration to an extracted or infusion configuration, activation means (44) which comprise a rotor (48), rotatable about a rotation axis (X-X) in an injection rotation direction (I) and in a control rotation direction (C), opposite each other.

Abstract: A medical device and system for the administration of a medical substance or for dosing body fluids comprising a rotor, rotating around an axis X-X, operatively connected to an injection device of said medical substance, and a rotor locking/unlocking device mechanically separate from the rotor and integral in rotation therewith. The locking/unlocking device comprises, in one piece, a disc, centered with respect to said axis X-X, from which a plurality of flexible fins radially unravel. The flexible fins are configured to flex around transverse hinges at a connection portion with the disc, and are angularly spaced so as to define gaps between adjacent pairs of fins which prevent interferences between adjacent fins in the respective flexing movement. The flexible fins are associated with ferromagnetic means for the operation of the same fins and locking/unlocking means of the rotation of the disc. The disc and fins are formed from a single plastic body.

Abstract: The present invention refers to a medical device for trans-dermal infusion of a medicament comprising a reservoir for holding a medicament to be infused, a pump for pumping medicament from the reservoir, wherein the device is assembled or adapted to be assembled in at least one pre-operational arrangement with or without the reservoir and is adapted to be rearranged from the at least one pre-operational arrangement into an operational arrangement comprising the reservoir. In particular, in the pre-operational arrangement without reservoir the pump is in a mechanically distressed condition preventing functional operation of the pump, and in the pre-operational arrangement comprising the reservoir the pump is in a mechanically distressed condition preventing functional operation of the pump and/or the reservoir is fluidically disconnected from the pump.

Abstract: Medical fluid-flow regulating devices are provided. Such medical fluid-flow regulating devices typically include a rotor and a flow-regulator element engaged or engageable with each other via a coupling that below a torque and/or fluidic-pressure threshold value allows the flow-regulator element to move upon rotation of the rotor and thereby regulate fluid flow. The medical fluid-flow regulating devices also include a blocking unit that above the torque and/or fluidic-pressure threshold value irreversibly blocks the rotor or the flow-regulator element or the coupling between the rotor and the flow-regulator element resulting in irreversible inactivation of the medical fluid-flow regulating device. Systems incorporating such medical fluid-flow regulating devices are also provided. Methods for detecting inactivation of such devices are also provided.

Abstract: A system for withdrawing blood from a body part that avoids formation of a drop of blood on the skin surface of the body part after blood removal. The system includes a collecting unit to withdraw blood, a lancing member configured for insertion into the body part and having a capillary to collect blood, and a pressure piece configured to apply pressure to the body part and having an actuator operably connected thereto. The pressure piece is movable relative to a support configured to exert pressure on the body part, and the actuator is configured to reduce the compressive force of the pressure piece after removing an amount of blood, whereby forming a drop of blood on the skin surface of the body part can be avoided.

Abstract: An infusion system for infusing a medication in a patient, comprising a medication dose dispensing device and a control device for controlling the dispensing device. The infusion system can be configured in a non-operating configuration, in which the dispensing device and the control device are spaced apart from each other, and in an operating configuration, in which the dispensing device and the control device are temporarily proximity-coupled. The actuating rotor of the control device and the actuated rotor of the dispensing device have a common rotation axes, and the system can compensate or block the rotation of the control device with respect to the dispensing device.

Abstract: System for trans-dermal delivery of doses of a medicament, comprising a delivery device to be placed in dermal contact with a patient, the delivery device comprising a reservoir for holding a medicament to be delivered, a trans-dermal injection element for delivering doses of the medicament to the patient, a control unit for controlling the delivery of the medicament when activated, the system further comprising a separate hand-held drive device to be temporarily placed in proximity of the delivery device when a dose of medicament is required, the drive device comprising an activation unit for activating the control unit of the delivery device.

Abstract: A rotor for medical flow-regulating devices is described. The rotor comprises a central body and a margin extending from the central body. The margin comprises at least one actionable section that is movable from a rest position to a stretched position with respect to the central body upon application of a force and is configured to resiliently return to the rest position upon removal of the force. A medical flow-regulating device comprising the rotor is also described. A system comprising the medical flow-regulating device and a hand-held activation device is also described. A method of manufacturing a rotor is also described.

Abstract: The present invention refers to a system for medical treatment comprising a medical device and a separate hand-held device. The medical device comprises an energy-receiving unit and the separate hand-held device comprises a housing and an energy-transfer unit to transfer energy to be used at least in part for performing medical treatment to the energy-receiving unit of the medical device when the energy-receiving unit and the energy-receiving unit are in an energy-transfer position. The system further comprises at least one position sensor adapted to detect at least when the energy-transfer unit and the energy-receiving unit are in the energy-transfer position. The system further comprises a controller for controlling the energy-transfer unit such that the transfer of energy needed for medical treatment from the energy-transfer unit to the energy-receiving unit is enabled only when the energy-transfer unit and the energy-receiving unit are in the energy-transfer position.

Abstract: A medical device and a system for medical treatment comprising the medical device are disclosed. The medical device comprises a fluidic conduit and/or is configured to be operatively coupled to a fluidic conduit. The medical device comprises a flow regulator for regulating the flow of a fluid in the fluidic conduit and at least two movable elements, which are passively displaceable as a function of a fluidic pressure change in the fluidic conduit or actively displaceable for regulating the flow of fluid in the fluidic conduit. The medical device further comprises at least one transponder circuit comprising at least one transponder element chosen from a capacitor, an inductor, a resistor, or combinations thereof, being arranged with respect to the movable elements such that the transponder circuit has a capacitance or inductance or resistance or resonant frequency or Q factor, which changes as a function of the displacement of the movable elements.

Abstract: Medical fluid-flow regulating devices are provided. Such medical fluid-flow regulating devices typically include a rotor and a flow-regulator element engaged or engageable with each other via a coupling that below a torque and/or fluidic-pressure threshold value allows the flow-regulator element to move upon rotation of the rotor and thereby regulate fluid flow. The medical fluid-flow regulating devices also include a blocking unit that above the torque and/or fluidic-pressure threshold value irreversibly blocks the rotor or the flow-regulator element or the coupling between the rotor and the flow-regulator element resulting in irreversible inactivation of the medical fluid-flow regulating device. Systems incorporating such medical fluid-flow regulating devices are also provided. Methods for detecting inactivation of such devices are also provided.

Abstract: A system for withdrawing blood from a body part that avoids formation of a drop of blood on the skin surface of the body part after blood removal. The system includes a collecting unit to withdraw blood, a lancing member configured for insertion into the body part and having a capillary to collect blood, and a pressure piece configured to apply pressure to the body part and having an actuator operably connected thereto. The pressure piece is movable relative to a support configured to exert pressure on the body part, and the actuator is configured to reduce the compressive force of the pressure piece after removing an amount of blood, whereby forming a drop of blood on the skin surface of the body part can be avoided.

Abstract: A rotor for medical flow-regulating devices is described. The rotor comprises a central body and a margin extending from the central body. The margin comprises at least one actionable section that is movable from a rest position to a stretched position with respect to the central body upon application of a force and is configured to resiliently return to the rest position upon removal of the force. A medical flow-regulating device comprising the rotor is also described. A system comprising the medical flow-regulating device and a hand-held activation device is also described. A method of manufacturing a rotor is also described.

Abstract: A microfluidic system having a microchannel for the capillary transport of a liquid, in particular a body fluid for analytical purposes. The microchannel is provided with a surface coating comprising at least one hydrophilic substance selected from the group consisting of polyacrylic acid, polyacrylate, dextran sulfate and chondroitin sulfate. The invention also concerns a coating method that is suitable for this.

Abstract: A medical device and a system for medical treatment comprising the medical device are disclosed. The medical device comprises a fluidic conduit and/or is configured to be operatively coupled to a fluidic conduit. The medical device comprises a flow regulator for regulating the flow of a fluid in the fluidic conduit and at least two movable elements, which are passively displaceable as a function of a fluidic pressure change in the fluidic conduit or actively displaceable for regulating the flow of fluid in the fluidic conduit. The medical device further comprises at least one transponder circuit comprising at least one transponder element chosen from a capacitor, an inductor, a resistor, or combinations thereof, being arranged with respect to the movable elements such that the transponder circuit has a capacitance or inductance or resistance or resonant frequency or Q factor, which changes as a function of the displacement of the movable elements.

Abstract: System for trans-dermal delivery of doses of a medicament, comprising a delivery device to be placed in dermal contact with a patient, the delivery device comprising a reservoir for holding a medicament to be delivered, a trans-dermal injection element for delivering doses of the medicament to the patient, a control unit for controlling the delivery of the medicament when activated, the system further comprising a separate hand-held drive device to be temporarily placed in proximity of the delivery device when a dose of medicament is required, the drive device comprising an activation unit for activating the control unit of the delivery device.