Patent classifications
A61J1/2075
MANIFOLD FOR AUTOMATIC DRUG COMPOUNDER
A manifold for control of fluid and/or vapor flow between a container and a pump cartridge for a compounder system is provided. One or more manifolds may be disposed in a magazine configured to secure and align the manifolds with a plurality of ports in the cartridge. Each manifold may include a needle having forward and rear openings to a central bore. A needle housing may include a slot configured to receive a push rod for actuating the needle forward and backward. In a forward, engaged position, the openings in the needle may be disposed on opposite sides of a sealing member of the manifold to form a fluid pathway through the manifold. In a rearward, disengaged position, both the forward and rear openings in the needle may be disposed on the same side of the sealing member to prevent fluid and vapor from flowing through the manifold.
Pressure-regulating vial adaptors
In certain embodiments, a vial adaptor comprises a housing configured to couple the adaptor with a vial, an access channel, a regulator channel, and a regulator assembly. The access channel is configured to facilitate withdrawal of fluid from the vial when the adaptor is coupled to the vial. The regulator channel is configured to facilitate a flow of a regulating fluid from the regulator assembly to compensate for changes in volume of a medical fluid in the vial. The regulator assembly can include a valve configured to transition between a closed configuration and an opened configuration.
RECEPTACLE FOR HOLDING AN ACTIVE SUBSTANCE AND CORRESPONDING CAP AND CONTAINER
A receptacle is designed for a chamber for an active substance. The receptacle includes two main elements. A first element is a transverse wall with a first main side facing an interior of the chamber, and a peripheral wall formed with the first main side of the transverse wall. A second element includes a bottom wall and a sheath extending from the bottom wall. The peripheral wall and the sheath surround one another and are in contact with each other so that the chamber is formed between the bottom wall, the transverse wall, the peripheral wall and/or the sheath. At least one ventilation groove is provided between the peripheral wall and the sheath form a ventilation channel connecting the chamber with the outside atmosphere.
MEDICAL FLUID TRANSFER AND INJECTION APPARATUS AND METHOD
Drug delivery system, injection device, transfer apparatus, vial holder and method of administering and transferring are disclosed which provide for passive warming of chilled injectable transferred through the transfer apparatus and into the injection device. The injection device may include a skin-facing surface including a skin boundary displacement extension or structure around a needle injection site to create a high pressure zone in the tissue. Radio frequency tracking and monitoring features for tracking patient compliance also may be provided.
MEDICINAL FLUID DELIVERY DEVICE
In some embodiments, a reconstitution or medicinal fluid delivery device includes a transfer engine including two fluidly connected spikes, each configured to pierce a container. A check valve may be disposed between the two spikes to allow unidirectional flow from one container to the other. Physical access to a fluid outlet may be obstructed by a housing until the reconstitution or medicinal fluid delivery device is actuated, whereupon physical access to the fluid outlet is permitted. The reconstitution or medicinal fluid delivery device may be placed on a flat surface and actuated with force applied in a single direction toward the flat surface.
Hollow Needle Assembly
A hollow-needle assembly is part of a transfer apparatus that serves for transferring a liquid between a storage container and a further use container. The hollow-needle assembly has a hollow needle having a pointed needle end. A liquid duct for transporting liquid through the hollow needle and out of the latter leads out via at least one liquid-duct opening in the region of the free needle end. An aeration gas duct that likewise leads out via a gas-duct opening in the region of the free needle end serves for transporting gas through the hollow-needle assembly. Duct paths of the at least one liquid duct and of the at least one aeration gas duct extend separately from one another. The ducts lead out adjacently to one another axially along the hollow needle and in a manner offset from one another in the circumferential direction. A needle separating edge that extends in the longitudinal direction of the hollow needle extends between in each case one liquid-duct opening and an adjacent gas-duct opening in the circumferential direction. This results in reliable ventilation and venting of the storage container via the hollow needle when liquid is transferred.
SYRINGE APPARATUS FOR TRANSFERRING LIQUIDS INTO AND OUT OF A VIAL HAVING A SEPTUM
An apparatus for transferring a chosen quantity of medication from a vial to a container under sterile conditions is described. The present invention further facilitates dissolving solid medications contained in the vial or diluting concentrated medications contained in the vial, and transferring the resulting solutions to the container. The container may be an intravenous infuser.
SHIELDING DEVICE USEFUL FOR MANIPULATING A RADIOACTIVE SOLUTION
The present disclosure relates to a device (1) for sampling and/or injection of a radioactive solution (S) in a vial (2), wherein the vial (2) comprises an opening closed by a puncturable closure member (3). The device (1) comprises a container (7) adapted to receive said vial (2) and a vial adaptor (4), said vial adaptor (4) having a longitudinal axis (L1), provided at a first end (41) with a hollow spike (42) adapted to pierce said puncturable closure member (3) when the vial adaptor (4) is mounted on the vial (2), and at a second end (43) with connection means (5) adapted for its removable connection to a syringe (6), the container (7) comprising: a container body (71) adapted to receive said vial (2), the container body (71) having an opening (711), and a vial adaptor support structure (72) configured for being mounted onto the opening (711) of the container body (71), and comprising retention means configured for enabling releasable retention of said vial adaptor (4) within said vial adaptor support structure (72), and wherein the vial adaptor support structure (72) and the container body (71) are made at least partially of a radioprotective material for providing protection against ionizing radiation.
Dispenser for dispensing pharmaceutical liquids
Dispenser for dispensing pharmaceutical liquid having a housing, a liquid reservoir arranged within the housing, an exit opening through which liquid is discharged into a surrounding atmosphere, an outlet channel connecting the liquid reservoir to the exit opening and having an outlet valve, openable in a pressure-dependent manner or actuatable manually, arranged in the outlet channel. With the valve closed, the outlet channel is subdivided into a first portion upstream of the outlet valve and a second portion downstream of the outlet valve. The housing is of antibacterial design in the region of surfaces which are intended to come into contact with the liquid, wherein it is exclusively surfaces in the region of the second portion and/or of an outer surface of the housing which have this antibacterial design.
Pressure-regulating vial adaptors
In certain embodiments, a vial adaptor comprises a housing configured to couple the adaptor with a vial, an access channel, a regulator channel, and a regulator assembly. The access channel is configured to facilitate withdrawal of fluid from the vial when the adaptor is coupled to the vial. The regulator channel is configured to facilitate a flow of a regulating fluid from the regulator assembly to compensate for changes in volume of a medical fluid in the vial. In some embodiments, the regulator assembly includes a flexible member configured to expand and contract in accordance with changes in the volume of the medical fluid in the vial. In some embodiments, the flexible member is substantially free to expand and contract. In some embodiments, the flexible member is not partly or completely located in a rigid enclosure.