Abstract: A surgical fixation tool (10) includes at least one fixation member (12) which protrudes from a leg (16) of a proximal grasping portion (20). The at least one fixation member (12) includes a needle (28) with a sharp distal tip (29). The needle (28) protrudes distally from a support structure (30) that includes one or more sloped support surfaces (34, 36) that are sloped with respect to a needle shaft (27).

Abstract: A needle protection assembly, adapted to protect a tip of a hypodermic needle, comprising a shield adapted, in a protected operative orientation of the needle protection assembly, to shield the tip of the hypodermic needle, a locking element including at least one slot, the slot including at least three surfaces corresponding to three operative orientations of the shield, at least one slot engaging element, functionally associated with the shield, the slot engaging element being disposed within the slot of the locking element and movable relative thereto, between the surfaces, so as to transition the shield between the three operative orientations, and at least one biasing element, adapted for axial biasing of the shield, wherein the three operative orientations include a storage operative orientation, an injection operative orientation, and a needle protection operative orientation.

Abstract: A needle protection assembly, adapted to protect a tip of a hypodermic needle, comprising a shield adapted, in a protected operative orientation of the needle protection assembly, to shield the tip of the hypodermic needle, a locking element including at least one slot, the slot including at least three surfaces corresponding to three operative orientations of the shield, at least one slot engaging element, functionally associated with the shield, the slot engaging element being disposed within the slot of the locking element and movable relative thereto, between the surfaces, so as to transition the shield between the three operative orientations, and at least one biasing element, adapted for axial biasing of the shield, wherein the three operative orientations include a storage operative orientation, an injection operative orientation, and a needle protection operative orientation.

Abstract: A method for monitoring blood vessels, the method including using a system for monitoring blood vessel functionality to look, listen and feel blood vessel functionality by imaging a patient's body to obtain blood vessel geometry, imaging a patient body to obtain a shape of a location of the patient's body using image analysis, and analyzing vibrations of the patient's body at a location of the patient's body which includes the blood vessels. A method for monitoring blood vessel functionality, the method including illuminating one or more blood vessels through a patient's skin, capturing at least one image of the blood vessels, analyzing the at least one image, and calculating a parameter associated with blood vessel functionality based upon the image analysis. Related apparatus and methods are also described.

Abstract: A syringe assembly, comprising a syringe barrel having a forward end and a rearward end and being arranged along a longitudinal axis; a restricting element, moveably supported onto a portion of the syringe assembly and positionable in one of an injection disabling position and an injection enabling position in different operative orientations of the syringe assembly; a plunger rod assembly displaceable within the syringe barrel and operatively coupled with the restricting element; the plunger rod assembly having a restricting feature adapted to cooperate with the restricting element, such that when the restricting element in the injection disabling position, the plunger rod assembly is permitted to be displaced axially forwardly only up to a certain longitudinal extent relative to the syringe barrel and when the restricting element is in the injection enabling position, the plunger rod assembly is permitted to be further displaced axially forwardly relative to the syringe barrel.

Abstract: A manipulating device includes a hollow tube having a tube wall formed with distal cutouts that define at least one deformable member in the tube wall and proximal cutouts that define an actuator in the tube wall connected to the at least one deformable member. Movement of the actuator deforms the at least one deformable member from a first orientation to a second orientation.

Abstract: Provided is a device for injection into an interlayer of an organ of a subject. The device includes a needle having a size transitional portion terminating in a sharp needle distal tip. The device also includes an elongated tissue separator that is shiftable in the needle lumen. An actuator shifts the tissue separator in the needle lumen between a first position, in which the separator distal tip is fixedly positioned proximally to the needle distal tip, and a second position in which the separator distal tip is fixedly positioned a predetermined distance distally from the needle distal tip.

Abstract: A method for monitoring blood vessel functionality, the method including illuminating one or more blood vessels through a patient's skin, capturing at least one image of the blood vessels, analyzing the at least one image, and calculating a parameter associated with blood vessel functionality based upon the image analysis. A method for replacing a physical examination performed by medical staff for monitoring blood vessel functionality in dialysis patients, the method including producing at least one image of a patient organ instead of manually manipulating the patient's organ, analyzing the at least one image, and classifying the patient's status to be one of suitable for dialysis or at risk for dialysis. Related apparatus and methods are also described.

Abstract: Systems and devices for interfacing between a medicinal vial, a hypodermic needle, and an injection device such as a syringe, comprising a valve, functionally associated with said vial adaptor, said injection device port, and said needle, said valve having a first orientation wherein said injection device port is in fluid flow communication with said vial adaptor and a second orientation wherein said injection device port is in fluid flow communication with said hypodermic needle, wherein rotation of said injection device port between a first position and a second position thereof, drives transition of said valve from said first orientation to said second orientation.

Abstract: The invention provides a safe auto-needle device for injection, comprising: a main housing and a syringe-support receiving a disposable prefilled syringe terminating in a needle covered by a needle sheath (NS). The speed of depressing of the syringe plunger is manually controllable by a user. In a first embodiment, a locking mechanism is present, for preventing premature advancement of the needle. A second embodiment comprises an interlock, for preventing depressing of a plunger, prior to advancement of the syringe-support to a needle penetration location. Additional components include a drive mechanism; and a needle shield moveable between: a needle covered position; a partially exposed position, to a fully extended needle safe position. The invention also discloses a needle sheath (NS) remover.

Abstract: A needle protection assembly, adapted to protect a tip of a hypodermic needle, comprising a shield adapted, in a protected operative orientation of the needle protection assembly, to shield the tip of the hypodermic needle, a locking element including at least one slot, the slot including at least three surfaces corresponding to three operative orientations of the shield, at least one slot engaging element, functionally associated with the shield, the slot engaging element being disposed within the slot of the locking element and movable relative thereto, between the surfaces, so as to transition the shield between the three operative orientations, and at least one biasing element, adapted for axial biasing of the shield, wherein the three operative orientations include a storage operative orientation, an injection operative orientation, and a needle protection operative orientation.

Abstract: Systems and devices for interfacing between a medicinal vial, a hypodermic needle, and an injection device such as a syringe, comprising a valve, functionally associated with said vial adaptor, said injection device port, and said needle, said valve having a first orientation wherein said injection device port is in fluid flow communication with said vial adaptor and a second orientation wherein said injection device port is in fluid flow communication with said hypodermic needle, wherein rotation of said injection device port between a first position and a second position thereof, drives transition of said valve from said first orientation to said second orientation.

Abstract: A safe auto-needle device for injection, comprising: a main housing; a syringe-support for receiving a disposable prefilled syringe; said syringe comprises: a piston; a proximal end; and a distal end terminating in a needle covered by a needle sheath (NS); a drive mechanism for advancing said syringe-support distally towards an injection site; a tubular needle shield; moveable from: a needle covering position, to partially exposed, to needle irreversibly concealed; said generally tubular needle shield comprising a distal end for contacting an injection site, and a proximal end; a spring urging distal movement of said needle shield; and said needle shield comprising a spring seat; an NS remover, designed to mate with and irreversibly grip said NS, for removal of said NS prior to injection; a locking mechanism preventing premature advancement of said needle; a plunger rod for engaging said piston, wherein depressing of said plunger is manually controllable; wherein in use of said device, said NS remover is r

Abstract: The present disclosure provides for improved bone implantation and stabilization assemblies, and improved systems/methods for deploying and/or undeploying such bone implantation and stabilization assemblies. More particularly, the present disclosure provides for improved devices, systems and methods for stabilizing bones and/or bone segments. In exemplary embodiments, the present disclosure provides for improved devices, systems and methods for deploying bone implantation and stabilization assemblies into bone tissue (e g., spinal structure, vertebrae, cancellous bone, cortical bone, etc.) in order to stabilize bones and/or bone segments.

Abstract: An implant (300) for repair of a spinal inter-vertebral disc, constituted of a first section and a second section, each having: a support member section (110); a proximal support member secured to the proximal end of the support member section and arranged to extend proximally thereof, the proximal support member (170) arranged in a deployed configuration to distend in the direction of the first face (130) of the support member section (110); and a pair of one inter-annulus support members (170), each of the pair of inter-annulus support members optionally exhibiting a plurality of stacked layers, arranged so as to cooperating under ejection forces to act as a single layer, the support member section of the first section secured to the support member section of the second section such that the second face of the first section faces the second face of the second section.

Abstract: An implant (300) for repair of a spinal inter-vertebral disc, constituted of a first section and a second section, each having: a support member section (110); a proximal support member secured to the proximal end of the support member section and arranged to extend proximally thereof, the proximal support member (170) arranged in a deployed configuration to distend in the direction of the first face (130) of the support member section (110); and a pair of one inter-annulus support members (170), each of the pair of inter-annulus support members optionally exhibiting a plurality of stacked layers, arranged so as to cooperating under ejection forces to act as a single layer, the support member section of the first section secured to the support member section of the second section such that the second face of the first section faces the second face of the second section.

Abstract: An implant (10) arranged as a tubular member (20) with a longitudinal axis (80). The tubular member exhibits a proximal end (100) and a distal end (110), the distal end arranged to extend to within the inner region of an annulus. Inter-annulus support members (30) are arranged radially about the tubular member, and connected proximally of the distal end, thus defining an axial support member (120) between the connection to the tubular member and the distal end. Proximal securing members are further provided arranged radially about the tubular member and removed proximally from the connection point of the inter-annulus support members. The inter-annulus support members are connected to the axial support member such that ejection forces are opposed by a concavingly curved link member between the axial support member and the inter-annulus support members.

Abstract: The present disclosure provides for improved bone implantation and stabilization assemblies, and improved systems/methods for deploying and/or undeploying such bone implantation and stabilization assemblies. More particularly, the present disclosure provides for improved devices, systems and methods for stabilizing bones and/or bone segments. In exemplary embodiments, the present disclosure provides for improved devices, systems and methods for deploying bone implantation and stabilization assemblies into bone tissue (e g., spinal structure, vertebrae, cancellous bone, cortical bone, etc.) in order to stabilize bones and/or bone segments.

Abstract: A closed blood sampling system within a pressure monitoring line having a control valve that enables a clearance reservoir to be isolated from the pressure column when no samples are being taken. The valve is a stopcock-like device that includes a rotating valve member and attached control handle with clear visible and tactile indicators for the mode of operation. The rotating valve member has a number of internal and circumferential channels for connecting or disconnecting select ports in the core of the valve. By isolating the clearance reservoir, the quality of the pressure signal is improved such that the sampling line can be lengthened for greater convenience in the intensive care or operating room. The valve may also incorporate a blunt cannula sampling site therewithin.

Abstract: A closed blood sampling system within a pressure monitoring line having a control valve that enables a clearance reservoir to be isolated from the pressure column when no samples are being taken. The valve is a stopcock-like device that includes a rotating valve member and attached control handle with clear visible and tactile indicators for the mode of operation. The rotating valve member has a number of internal and circumferential channels for connecting or disconnecting select ports in the core of the valve. By isolating the clearance reservoir, the quality of the pressure signal is improved such that the sampling line can be lengthened for greater convenience in the intensive care or operating room. The valve may also incorporate a blunt cannula sampling site therewithin.