The present invention provides devices to access the suprachoroidal space or sub-retinal space in an eye via a minimally invasive transconjunctival approach. The devices may also be used after a partial dissection, for example after dissection of the outer scleral layer of the eye, and using the device within the dissection to access the suprachoroidal space or the sub-retinal space.

The invention relates to a syringe with a visual indicator and retaining elements, which is used in the application of epidural anaesthesia. The syringe has the particularity of comprising a visual indicator located at the front end of a plunger that drives the fluid contained in the barrel, which visual indicator is an element in the form of a bellows comprising two discs with a membrane between the two discs, wherein the membrane can be deformed according to the pressure in the syringe. The syringe also comprises longitudinal lateral flanges on the body of the plunger, which have a surface with a plurality of teeth, wherein the plunger is rotatable relative to its axial axis, and wherein the teeth allow the plunger to be secured.

In some embodiments, a tube portion can be configured to be fluidically coupled to a patient access component. A source of pressurized fluid can be coupled to the tube portion and can be configured to deliver fluid to the tube portion at a source pressure. A fluid pressure regulating device can include an expandable reservoir and can be coupled to the tube portion such that the expandable reservoir is in fluidic communication with the tube portion. The fluid pressure regulating device can be configured such that, when fluid is delivered from the source of pressurized fluid to the lumen of the tube portion at the source pressure, the expandable reservoir of the fluid pressure regulating device can receive fluid such that the expandable reservoir of the fluid pressure regulating device expands and fluid is delivered from the lumen of the tube portion to the patient via the patient access component.

A method and apparatus are provided for use in locating a target region which is situated in the body of a subject, for example for the delivery of drugs. The system includes an assembly for controlling the flow of fluid from a fluid reservoir to a conduit, such as a needle. A sensor detects a characteristic indicative of the fluid pressure in the conduit. The system processes data from the sensor to detect the presence of a pulsatile waveform. A controller may control further operation of the system based on information regarding the presence of the pulsatile waveform and features of the waveform, such as amplitude.

A method and apparatus are provided for use in locating a target region which is situated in the body of a subject, for example for the delivery of drugs. The system includes an assembly for controlling the flow of fluid from a fluid reservoir to a conduit, such as a needle. A sensor detects a characteristic indicative of the fluid pressure in the conduit. The system processes data from the sensor to detect the presence of a pulsatile waveform. A controller may control further operation of the system based on information regarding the presence of the pulsatile waveform and features of the waveform, such as amplitude.

The present invention will provide a medical device that can properly regulate the working pressure of a highly pressurized gas for delivering therapeutic agents at a relatively constant flow rate during the entire course of infusion while also maintaining the integrity of the operating room and reducing risks involved with therapeutic agents. This is accomplished utilizing a pressure control assembly along with a syringe assembly or self-contained fluid chamber to administer therapeutic agents to patents in a controlled and safe manner by incorporating pressurized gas.

A gear-driven infusion assembly is provided which has a housing, a gear assembly coupled to the housing, a shuttle assembly slidably coupled to the housing and operably coupled to the gear assembly, and a tube enclosure connected to the housing. The tube enclosure is configured to house a primary drug closure. The gear assembly includes a spool assembly having a pinion gear and a drive spool. When the spring rotates the drive spool, the drive spool drives the pinion gear, and the gear assembly drives the shuttle assembly. When the gear assembly drives the shuttle assembly, the shuttle assembly slides longitudinally along the housing. The gear assembly may be spring driven such that a spring rotates the pinion gear about the drive spool. The primary drug closure may be a syringe. An overspeed protection device is also provided which has a spool assembly including a drive spool having a plurality of cams, a spring, and a pinion gear with spiral cam surfaces.

An injection device for dispensing of a liquid medicament is disclosed. The device includes an elongated housing extending in an axial direction to accommodate a cartridge, a drive member axially displaceable inside the housing and being in sealed engagement with a side wall of the housing, wherein the drive member has an abutment face to axially abut with a proximal end of a barrel of the cartridge to displace the cartridge from the undeployed position towards the deployed position, wherein the drive member has an outlet located distally from the sealed engagement and further has an inlet located proximally from the sealed engagement, wherein the inlet and the outlet are in flow connection with each other via a flow path extending through the drive member and wherein at least one flow restrictor is arranged across or in the flow path.

An injection device for dispensing of a liquid medicament is disclosed. The device includes an elongated housing extending in an axial direction to accommodate a cartridge, a drive member axially displaceable inside the housing and being in sealed engagement with a side wall of the housing, wherein the drive member has an abutment face to axially abut with a proximal end of a barrel of the cartridge to displace the cartridge from the undeployed position towards the deployed position, wherein the drive member has an outlet located distally from the sealed engagement and further has an inlet located proximally from the sealed engagement, wherein the inlet and the outlet are in flow connection with each other via a flow path extending through the drive member and wherein at least one flow restrictor is arranged across or in the flow path.

A method and apparatus are provided for use in locating a target region which is situated in the body of a subject, for example for the delivery of drugs. The system includes an assembly for controlling the flow of fluid from a fluid reservoir to a conduit, such as a needle. A sensor detects a characteristic indicative of the fluid pressure in the conduit. The system processes data from the sensor to detect the presence of a pulsatile waveform. A controller may control further operation of the system based on information regarding the presence of the pulsatile waveform and features of the waveform, such as amplitude.