Abstract: A colored seal system, method, and apparatus. The colored seal system includes a barrel having a delivery end and an open end. The barrel includes multiple markings. The barrel markings include at least measurements and multiple fill indicators. The colored seal system includes a colored seal slidably positioned within the barrel for moving a delivery agent. The colored seal is visible within at least one of the fill indicators.

Abstract: Improved apparatus for use with medication in fluid form, which is particularly beneficial for medications having a relatively high viscosity. The disclosed syringe adapter has an opening that is relatively large, as compared to a conventional needle, and thus affixing the disclosed syringe adapter to a syringe improves syringeability of higher-viscosity medications. Some embodiments feature a lateral extension that prevents inserting the syringe adapter too far into a medicine bottle, and some embodiments feature a component that assists in firmly grasping. When the disclosed syringe adapter is affixed to a pistol-grip or tab-handled syringe, the medication withdrawn into the pistol-grip syringe can be more easily administered from the syringe barrel. In some embodiments, the syringe adapter will be replaced with a needle prior to injecting the medication, while in some other embodiments, the needle is affixed to the in-place syringe adapter for the injection.

Abstract: A system for automatically injecting a substance. The system includes an injecting device, which includes an injecting cartridge, a biasing mechanism and a latch. The injecting cartridge includes a syringe having a needle and a plunger, and an injecting mechanism for moving the syringe and pushing the plunger of the syringe. The injecting cartridge includes a needle and a plunger, and an injecting mechanism for moving the syringe and pushing the plunger of the syringe. The biasing mechanism pivots the injecting cartridge from a storage position into an injecting position. The latch is moveable from a holding position for holding the biasing mechanism in the storage position to a release position for releasing the biasing mechanism. The system may further comprise sensors to measuring physical signs of a user. The system may also include controller to control the automatic injection of the substance.

Abstract: A high-slidability syringe has high safety and sealability over a long period of time. The syringe includes a gasket having a lower sliding resistance to a syringe barrel. The syringe includes: a syringe barrel; a gasket adapted to be press-fitted in the syringe barrel and used in a sliding manner in the syringe barrel; and a piston rod with the gasket attached to a front end thereof. The gasket includes: a gasket main body that is formed of a rigid plastic having resistance to a drug solution to be loaded into the syringe barrel and has a recessed groove formed in a sliding contact surface thereof adapted to slidably contact an inner circumferential surface of the syringe barrel; and a sliding contact ring that is fitted in the recessed groove.

Abstract: The present disclosure relates to a cap for an injection device. The injection device comprises a body for holding a syringe having a needle extending from an end thereof. The cap is removably attachable to the body. The cap comprises an actuator and a needle shield to cover said needle. The cap further comprises a coupling between the actuator and the needle shield. The coupling is configured such that when the cap is attached to the body of an injection device axial movement of the actuator away from the body causes rotation of the needle shield relative to the body.

Abstract: Provided is an iontophoresis device. An iontophoresis device according to an embodiment of the present invention includes a power supply unit configured to supply power; two electrodes configured to supply current to a user's skin when brought into contact with the skin, thereby allowing an ionic drug or an active ingredient applied to the user's skin to permeate the skin by an electrical repulsive force; and a control unit configured to adjust an output value of a voltage or a current applied to the electrodes according to the user's skin condition, thereby allowing the user to feel a uniform intensity of electrical stimulation.

Abstract: The invention provides methods and apparatus for injecting a medicine, especially a highly viscous medicine. Conventional methods and apparatus for injecting viscous medicines suffer from a variety of problems such as excessive force during the initial needle insertion and initial injection. In an inventive method, during the initial phase of the injection, energy is stored in a torsion spring that is subsequently released during a later stage of the injection. The present invention also provides for an improved autoinjector; especially via the use of a combination compression and torsion spring that powers the injection through controlling force applied to a plunger via a screw flange or nut having pins that ride in a prescribed path down the length of the autoinjector.

Abstract: The present disclosure relates to an injection device. The injection device comprises a body for holding a syringe that has a needle at one end and a cap that is removably attached to the body. The cap has a needle shield to cover said needle. The injection device further comprises an actuator member and a translating member. The actuator member is pivotally coupled to one of the cap or body. The translating member is connected to the actuator member and is configured such that pivotal movement of the actuator member relative to said one of the cap or body causes movement of the translating member relative to the body to urge the needle shield away from the body.

Abstract: An injection needle includes a needle hub and a needle tube. The needle hub is connected to a safety protective cover by an elastic flip mechanism. Two symmetrically-distributed needle hub hooks are provided on a side wall of the needle hub. Two symmetrically-distributed protective cover snaps are provided in a hollow inner cavity of the safety protective cover. The two protective cover snaps cooperates with the two needle hub hooks. Protective cover snap stoppers are provided on outer sides of the two protective cover snaps. The injection needle employs the two needle hub hooks disposed on the side wall of the needle hub and cooperate with the two protective cover snaps disposed in the inner cavity of the safety protective cover.

Abstract: Vitreoretinal instruments and methods related thereto are disclosed herein. The disclosure describes various example vitreoretinal instruments having various aspirating port configurations. A vitreoretinal instrument may include a handle and a cannula coupled to the handle. The cannula may include a straight portion and a curved portion. The curved portion may be configurable between a straight configuration and a curved configuration. The curved configuration may include a first curved portion having a curvature defined by a first radius. The curved configuration may include a second curved portion having a curvature defined by a second radius different from the first radius. The curved portion may further include one or more ports formed in the curved portion.

Abstract: An example system for administrating a liquid medication includes a syringe assembly including a barrel portion containing liquid medication, a plunger portion sealingly engaged with the barrel portion to form a chamber for expelling the liquid medication from the barrel portion, and a needle. A ring is positioned about the plunger portion of the syringe assembly, wherein the ring limits movement of the plunger portion in an axial direction as the plunger portion is moved in the axial direction to administer a first dose of the liquid medication. The ring is configured to be modified to allow the plunger to move further in the axial direction to administer a second dose of the liquid medication.

Abstract: A method to dispense medication using one or more fillable medical dispensers by providing the medical dispenser with a first predetermined medication dosage sufficient for a first predetermined dispensing period, wherein the first dispensing period ends on a first repetitive day of the week for ease of remembrance by a user; providing the medical dispenser with a second predetermined medication dosage sufficient for a second predetermined dispensing period, wherein the dispensing period ends on a second repetitive day of the week for ease of remembrance; and installing the medical dispenser at least twice a week at a repetitive weekly replacement schedule.

Abstract: A catheter, including a catheter body and a connector, can be adapted to a syringe for nasal flushing treatment. The catheter body is made of a soft material and has a flat closed distal end, a transitional segment having a flat closed segment and a lumen-containing oval segment, a circular normal segment and an open end on the opposite side of the flat closed distal end as well as multiple side-holes disposed near the closed end so that the catheter can be operated by patient to insert into a slit space of nasal cavity smaller than the diameter of the circular normal segment.

Abstract: A device includes: a first member comprising a first-member-side power transmission part; and a second member comprising a second-member-side power transmission part configured to be attachable to and detachable from the first member, the second member being a part of a medicinal-liquid administering device. The first-member-side power transmission part and the second-member-side power transmission part are configured to be engaged with each other for administering a medicinal liquid into a living body. The second member is configured to open a housing covering the first-member-side power transmission part to engage the second-member-side power transmission part with the first-member-side power transmission part at a time of attaching the first member to the second member.

Abstract: A catheter assembly includes: a catheter; a hollow inner needle that is removably disposed in the catheter and has a lumen through which a guide wire is insertable; a needle hub that is fixed to a proximal end portion of the inner needle; and a guide member that is attachable to a proximal end portion of the needle hub and configured to guide the guide wire towards the inner needle.

Abstract: An enema device and a method for using the same are disclosed. The enema device includes a non-plastic container and a liquid delivery tube. The non-plastic container is made of glass, stainless steel, or ceramic. The non-plastic container includes a bottom wall and an annular sidewall extending upwardly from the peripheral of the bottom wall, wherein the bottom wall has a bottom planar surface. The liquid delivery tube is in fluid communication with a containing chamber of the non-plastic container. Therefore, harmful effects to the human body from plasticizer can be prevented.

Abstract: A balloon catheter includes a shaft, and a balloon provided outside the shaft. A drug is provided on an outer surface of the balloon, and the balloon has at least a straight tube part. A change ratio of an outer diameter of the straight tube part, (D28?D24)/D24, is 1.1% or less. D24 is the outer diameter of the straight tube part when an internal pressure of 2.43 MPa (24 atm) is applied, and D28 is the outer diameter of the straight tube part when an internal pressure of 2.84 MPa (28 atm) is applied.

Abstract: The present disclosure relates to an administration mechanism for a medicament delivery device having a movable sleeve, and a delivery member cover having a distal end portion configured to receive the movable sleeve. The delivery member being configured to be linearly displaceable between a first position and a second position relative to the movable sleeve, wherein the distal end portion has an end face defining a guide surface and the movable sleeve has a radially outwards extending first follower structure configured to cooperate with the guide surface when the delivery member cover is moved from the first position towards the second position, causing the movable sleeve to rotate.

Abstract: A method for the fail-safe termination of in vivo drug delivery from an implantable drug delivery system, the method comprising: providing an implantable drug delivery system comprising: a housing having a reservoir for containing a drug, and a port for dispensing the drug to a patient; and an emergency deactivation unit disposed between the reservoir and the port, the emergency deactivation unit comprising a composite structure comprising a biocompatible ferromagnetic mesh open to fluid flow and a hydrophobic meltable material, the hydrophobic meltable material comprising at least one hole therein for enabling a fluid to pass through the hydrophobic meltable material; implanting the implantable drug delivery system within a patient; enabling the drug to flow from the reservoir, through the at least one hole in the hydrophobic meltable material and out the port; and when drug flow is to be terminated, applying a magnetic field to the composite structure, such that a current is induced in the ferromagnetic mes

Abstract: The present invention is related to a vaginal drug delivery device and to a vaginal diagnostic device that comprises a first and second rigid member, wherein the first and/or second rigid member comprises a reservoir holding a medicament to be delivered, an opening, and a pump for pumping said medicament out of said opening, and/or wherein the first rigid member and/or second rigid member comprises a diagnostic device for performing an intravaginal diagnosis or measurement therefor. The device further comprises a first flexible member and flexible part, wherein at least one of the first flexible member and the flexible part is at least partially elastic having an elasticity such that the device can be squeezed from an extended shape to a collapsed shape. The device is pre-biased to assume the extended shape when little to no external force is being applied thereto.