Patent classifications
A61M5/178
INJECTION DEPTH INDICATION VIA INJECTION NEEDLE ILLUMINATION
A medical device includes a head having a base and a piercing member fluidly connected to the base. The medical device includes a tube having a proximal end, a distal end, a first central channel extending from the proximal end to distal end, and a longitudinal axis extending substantially centrally through the first central channel, the distal end of the tube being removably attached to the base. The medical device includes a plunger slidably disposed partly within the first central channel of the tube, the plunger defining a second central channel, and the longitudinal axis extending substantially centrally through the second central channel. In some examples, the medical device includes an optic assembly having a light source and a light pipe that is disposed partly within the second central channel and being configured to receive radiation emitted by the light source; and direct the radiation through the piercing member.
Dental needle vibration device
The Dental Needle Vibration Device comprises a vibrator motor device that may be formed onto a disposable dental or surgical needle, or may be reversibly coupled to a self-aspirating syringe. The Dental Needle Vibration Device couples to the disposable dental needle or self-aspirating syringe so that vibration motion from the vibrator motor is transmitted to the needle, improving control over the needle during vibration. The device is formed onto a disposable dental or surgical needle so that it does not rotate about the needle or move along the barrel of the needle. The device is coupled onto a self-aspirating syringe so that it is proximate to the needle in a fixed position so that it does not rotate about the syringe or move along the barrel of the syringe.
Accessory for an injection device including a pivotable cover
An accessory for an injection device having a needle cap. The accessory comprises a body portion comprising a recess adapted to receive the injection device and a cover coupled to the body portion. The cover is pivotally moveable between an open position in which the recess is exposed to receive the injection device, and a closed position in which the cover at least partially closes the recess to hold the injection device in the body portion. The accessory further comprises a cap remover comprising a grip adapted to hold the needle cap. The cap remover is moveable with respect to the body portion.
Vial Transfer and Injection Apparatus and Method
Drug delivery system, injection device, transfer apparatus, vial holder and method of administering and transferring are disclosed. The system may include transfer apparatus and an injection device. The transfer apparatus may have receiving stations for a drug source, such as a vial or vial holder, and for an injection device, and fluid flow pathways for transferring drugs from the source into the injection device. The injection device may include an expandable elastic bladder and an injection cannula that is movable between a plurality of positions.
Switch Assembly for an Electronic System of a Drug Delivery Device
The present disclosure refers to a switch assembly for an electronic system of a drug delivery device. The switch assembly includes a chassis supporting a PCBA including at least a first electrical contact, a second electrical contact, a third electrical contact and a fourth electrical contact and a ring with a ratchet profile. The chassis moves axially relative to the ring from a first axial position to a second axial position during a first switch operation mode. The chassis and the ring are configured such that the ring rotates relative to the chassis during a second switch operation mode. The first electrical contact and the second electrical contact are arranged such that upon axial movement of the chassis towards the ring during the first switch operation mode, an electrical connection between the first electrical contact and the second electrical contact is closed.
Delivery system and method for the effective, reliable and foolproof delivery of controlled amounts of a medical fluid
A method for performing a medical procedure requiring effective, reliable and foolproof delivery of controlled amounts of a medical grade gas to a patient includes providing a compressed gas cylinder having a weight with medical grade gas sealed therein of at least twelve grams and not greater than fifty grams. The method also includes connecting the compressed gas cylinder to an integrated compressed gas unit including a regulator valve assembly positioned between an outlet port and an inlet port, wherein the regulator valve assembly includes a press button actuator and regulator adjustment dial. A flow control system is secured to the compressed gas unit and the medical grade gas is delivered in precisely controlled amounts by actuating the compressed gas unit and operating the flow control system to deliver the medical grade gas to vasculature of the patient.
Delivery system and method for the effective, reliable and foolproof delivery of controlled amounts of a medical fluid
A method for performing a medical procedure requiring effective, reliable and foolproof delivery of controlled amounts of a medical grade gas to a patient includes providing a compressed gas cylinder having a weight with medical grade gas sealed therein of at least twelve grams and not greater than fifty grams. The method also includes connecting the compressed gas cylinder to an integrated compressed gas unit including a regulator valve assembly positioned between an outlet port and an inlet port, wherein the regulator valve assembly includes a press button actuator and regulator adjustment dial. A flow control system is secured to the compressed gas unit and the medical grade gas is delivered in precisely controlled amounts by actuating the compressed gas unit and operating the flow control system to deliver the medical grade gas to vasculature of the patient.
Stabilized formulations containing anti-IL-33 antibodies
The present invention provides pharmaceutical formulations comprising an antibody that specifically binds to human interleukin-33 (hIL-33). The formulations may contain, in addition to an anti-IL-33 antibody, a buffer, at least one amino acid, at least one sugar, or at least one non-ionic surfactant. The pharmaceutical formulations of the present invention exhibit a substantial degree of antibody stability after storage for several months and after being subjected to thermal and other physical stresses.
Device and method to locate site of intramuscular injection
Devices, kits and methods for determining the site of intramuscular injection in adult and child patients are disclosed. The device includes a top element and two legs that are configured to be fastened in a first position and a second position. When placed in the first position and second position, the device forms a substantially triangular region having a center that corresponds to the site of injection.
VIAL ADAPTOR ASSEMBLY FOR A CLOSED FLUID TRANSFER SYSTEM
A vial adaptor assembly, suitable for use with a vial containing a medicament and a syringe adaptor, which is in turn connectable to a syringe having a piston adapted for selectable displacement in a first direction for drawing fluid into the syringe and in a second direction for expelling fluid from the syringe, the vial adaptor assembly including: a vial connector for non-removable connection with the vial containing a medicament: a syringe adaptor connector for connection with the syringe adaptor; a pressure equalization chamber having a variable volume, which is scaled from the outside environment during use; a liquid pathway communicating between an interior of the vial containing the medicament and an interior of the syringe when the syringe adaptor is connected to the syringe adaptor connector and the syringe is connected to the syringe adaptor and the vial connector is connected to the vial containing the medicament; and a venting pathway communicating between the interior of the vial containing the medicament and an interior of the pressure equalization chamber, when the vial connector is connected to the vial containing the medicament, wherein the pressure equalization chamber and the venting pathway are mutually configured such that, when the syringe adaptor is connected to the syringe adaptor connector and the syringe is connected to the syringe adaptor and the vial connector is connected to the vial containing the medicament, substantially all of any of the medicament that becomes located within the pressure equalization chamber is removed therefrom via the venting pathway and returned to the interior of the vial by displacement of the piston of the syringe in the first direction.