Abstract: The invention is an accessory configured to be fitted to an electrical surgical device and provide suction at a surgical site in which the electrical surgical device is being used. In particular, the accessory is in the form of a suction collar configured to be releasably coupled to the electrical surgical device, generally adjacent to a working end thereof, and provide suction to minimize the accumulation of excess steam, fluid, and/or debris from the surgical site during the treatment procedure. The suction collar is further configured to apply a sufficient suction force to a patient's skin surrounding the surgical site to aid in stabilizing the electrosurgical device in place and maintain the working end to the electrosurgical device within the surgical site during the procedure.

Abstract: A bodily fluid collection system includes a reduced pressure treatment unit for providing reduced pressure to a fluid collection system through a canister having a container with an inlet adapted to be fluidly coupled to the fluid collection system, an outlet adapted to be connected to a source of reduced pressure, and an absorptive lamination disposed within the container. The absorptive lamination may be formed from a plurality of absorptive layers and wicking layers interleaved between the absorptive layers that collectively manifold bodily fluids from a tissue site into and throughout the absorptive lamination to trap and collect the bodily fluids. The container expands as the absorptive lamination swells with the bodily fluid being collected.

Abstract: Disclosed herein is a fully implantable artificial heart. The use of flat helical springs to align and reciprocate a bellows structure allows the bellows to pump blood, the multiple solenoids with floating magnetized rods and permanent magnet assemblies held by the flat helical springs provide the power. The artificial heart pumps blood with virtually no friction and no parts to wear out. The use of solenoids advantageously move blood in a gentle, controllable manner.

Abstract: The systems, devices, and methods presented herein use a blood pump to obtain measurements of cardiac function. The system can quantify the functioning of the native heart by measuring certain parameters/signals such as aortic pressure or motor current, then calculate and display one or more cardiac parameters and heart function parameters, such as left ventricular pressure, left ventricular end diastolic pressure, or cardiac power output. These parameters provide valuable information to a user regarding current cardiac function, as well as positioning and function of the blood pump. In some embodiments, the system can act as a diagnostic and therapeutic tool.

Abstract: Systems and methods for cleaning and disinfecting a medical therapy device that delivers any one of hemodialysis, hemodiafiltration and hemofiltration. The system has a base module that has at least one segment of a controlled compliant flow path and at least one pair of jumpered ports configured on the base module. One or more components have connections connectable to the jumpered ports of the base module to provide for fluid communication between the segment of the controlled compliant flow path in the base module and a flow path defined by the one or more components. The base module is connected to the one or more components that define a flow path configurable for carrying out in part at least one function performed during any one of hemodialysis, hemodiafiltration or hemofiltration.

Abstract: A dialysis system for determining an amount of total chlorine in a partially purified water sample is disclosed. The system includes a water machine that produces at least partially purified water including an at least partially purified water sample and a dialysis machine that provides a dialysis treatment to a patient. The dialysis machine receives the at least partially purified water from the water machine to prepare dialysis fluid for the dialysis treatment. The system also includes a total chlorine detector configured to receive the at least partially purified water sample, at a first time apply a source voltage to the at least partially purified water sample, and at a second time stop applying the source voltage to the at least partially purified water sample and instead monitor a sensed electrical parameter to determine an amount of total chlorine in the at least partially purified water sample.

Abstract: A personalized chronic care system including (i) a sensor; (ii) a data receiving device separate from the sensor and configured to receive data directly or indirectly from the sensor; (iii) a data analytics device separate from the sensor and including at least one algorithm configured to analyze the sensor data and provide an analyzed data outcome; and (iv) at least one output device separate from the sensor and in communication with the data analytics device, the at least one output device configured to receive and communicate the analyzed data outcome to a health care provider.

Abstract: A dialysis machine, in particular a peritoneal dialysis machine, with one or more of the following components: at least one receptacle, in particular a bag, to receive fresh or used dialysate, at least one tubing set to conduct a liquid, in particular dialysate, at least one patient catheter for the uptake and/or discharge of dialysate into or from the patient's abdominal cavity, whereby at least one of the components is provided with at least one sensor designed to measure at least one parameter value of the dialysate and which is also designed to transmit the parameter value to at least one receiver.

Abstract: Various types of a medical device are described which is used as an implantable renal replacement therapy (an implantable artificial kidney). This device removes toxins and excess water from blood of patients with kidney failure or end stage renal disease. Additionally, other configurations of the device can be used as an external (extracorporeal) device.

Abstract: An extracorporeal system for lung assist includes a housing which includes a blood flow inlet in fluid connection with a pressurizing stator compartment, a fiber bundle compartment in fluid connection with the pressurizing stator compartment via a flow channel within the housing, and a blood flow outlet in fluid connection with the fiber bundle compartment. An impeller is rotatably positioned within the pressurizing compartment for pressurizing blood entering the pressurizing stator compartment from the blood flow inlet. The system further includes a fiber bundle positioned within the fiber bundle compartment. The fiber bundle includes a plurality of hollow gas permeable fibers. The plurality of hollow gas permeable fibers is adapted to permit diffusion of gas between blood and an interior of the hollow gas permeable fibers. The plurality of hollow gas permeable fibers is positioned such that blood flows around the plurality of hollow gas permeable fibers when flowing through the fiber bundle compartment.

Abstract: An irrigation system for a surgical instrument includes an irrigation tube arranged to convey an irrigation fluid and an irrigation clip structurally arranged to receive a portion of the irrigation tube. The irrigation clip includes a proximal portion, a distal portion, a body portion, and an arm portion. The arm portion is structurally configured to selectively attach the irrigation clip to the surgical instrument and to bias the irrigation clip toward the surgical instrument with a biasing force. The irrigation clip includes a tube locking portion structurally arranged to cooperate with the surgical instrument to engage the outer surface portion of the irrigation tube to inhibit rotation and axial displacement of the irrigation tube relative to the irrigation clip in response to the biasing force.

Abstract: A syringe packaging system that includes a packaging member defining a first compartment, a second compartment, and a third compartment that are in gaseous communication theretogether is disclosed. The first compartment is structured to receive a syringe barrel therein, the second compartment is structured to receive a plunger rod therein, and the third compartment is structured to receive an oxygen absorber therein. With the packaging member enclosing the syringe barrel, the plunger rod, and the oxygen absorber, the oxygen absorber is adapted to draw oxygen from within the syringe barrel and to absorb oxygen contained within at least one of the first compartment, the second compartment, and the third compartment of the packaging member. The syringe packaging system of the present disclosure also allows for reduced storage space of a syringe assembly.

Abstract: A fluid infusion apparatus (100) used for administering a medication to a patient comprises: a reservoir (101) used for storing infusion fluid; a plunger (102) located within the reservoir (101) and limiting the infusion fluid together with the reservoir (101), wherein the plunger (102) is configured to be movable along the reservoir (101); an injection button (103) operatively and synchronously moving with the plunger (102) and configured to be operable; and a displacement limiting mechanism arranged parallel to the reservoir (101), and configured to limit the plunger (102) to move for a predetermined distance within the reservoir (101) when the injection button (103) is operated, thus dispensing a predetermined amount of the fluid stored in the reservoir (101). Implementing the above apparatus reduces the overall size of the apparatus and simplifies the setting process of the injection amount, thus facilitating the administration for users.

Abstract: A medical fluid bag rack for hanging bags containing medical fluid that includes at least one base section; at least two support arms which extend from the base section; and at least one bag rack arm. The at least one bag rack arm extends from the base section or from one of the support arms. Also disclosed are methods for manufacturing the fluid bag rack and devices.

Abstract: A method for managing use of a disposable with an infusion pump is provided. The method can include adding validity information about a particular set of disposables to a list of disposables. Subsequent to adding the validity information, the method can include modifying the validity information about the particular set of disposables on the list of disposables. The method can include an infusion pump reading identifying information from a disposable, and can include determining whether the disposable is valid for use, based at least in part upon comparison of the identifying information read from the disposable by the infusion pump with the validity information about the particular set of disposables on the list of disposables. The method can also include the infusion pump making a determination of whether to deliver or not deliver an infusate based at least in part upon the determining whether the disposable is valid for use.

Abstract: The invention relates to a method for detecting an occlusion in an infusion line (200) during an infusion process comprising the steps of receiving a periodically measured value of a force (F) that is applied by a pumping device (1) to push a liquid through the infusion line (200) and that is indicative of the pressure (P) in the infusion line (200), and subtracting from the measured force value (F) a frictional force component (F0), that is indicative of a true frictional force, for correcting the measured force value (F) by the true frictional force. The method is characterized in that the value of the frictional force component (F0) is periodically updated throughout the infusion process by applying an equation that comprises a term that takes into account the measured force (F).

Abstract: Disclosed herein are devices, systems, and methods that automate the identification of the start and end of a fluid bolus and calculate the volume of fluid given during the challenge. A flow measurement device is used to measure fluid flow in a conduit (e.g., IV tubing) and an algorithm is used to determine a start time and the stop time of a fluid bolus. In addition, the volume of fluid given during the bolus is calculated. Advantageously, this provides accurate and automatic collection of the start time of the fluid bolus, the income of the fluid bolus, and the volume of the fluid bolus. Historically, these data are estimated by the clinician used to assess the hemodynamic response to the fluid bolus.

Abstract: A system allows for collection and re-use of a fluid medium derived from diverting at least some of the fluid medium of an injection. The system comprises a sterile container, an injector, a delivery catheter, a flow diverter assembly and a diversion reservoir assembly. The delivery catheter is in communication with a selected site within a patient's body. The flow diverter assembly is disposed in a flow path between the injector and the delivery catheter and is configured to divert at least a portion of a medium of the injection from the flow path. The diversion reservoir assembly has a reservoir chamber fluidly coupled to the flow diverter assembly The reservoir chamber is configured to receive the diverted portion of the fluid medium to allow re-use by the medium injector of the diverted portion.

Abstract: Power and control systems for a drug delivery device allow for the activation, control of, and communication with the drug delivery device. The power and control system allows for a delay between device activation, and optionally needle insertion, and commencing drug delivery. The delay may be for a predetermined time. In addition, the power and control system may communicate with one or more external sensors and devices. The inputs from the sensors and devices may automatically, or on demand, adjust the delivery parameters of the device. The power and control systems may control a drive system that delivers a fluid at a variable rate or profile, allowing for the delivery to be tailored to maximize the effectiveness of the treatment.

Abstract: The present disclosure provides systems that include a flow probe that senses fluid flow or mass flow of fluid delivery to a patient. Based at least in part on the sensed fluid or mass flow, the flow probe provides flow-related data (e.g., volume or mass flow rate) that the system uses to derive a volume of fluid being delivered. The fluid can be delivered from an IV bag, another in-line port, or a combination of the two. The disclosed systems provide fluid volume and/or fluid rate for display to a clinician and an informative understanding of what volume of fluid/mass a patient has received.

Abstract: Provided are a biosensor and a method for forming the same, a glucose control system, a method for forming the glucose control system, and a method for controlling glucose using the glucose control system. The biosensor comprises at least one sensor comprising a sensing unit, a bridge unit connected to the sensing unit, and an electrode unit connected to the bridge unit, wherein the sensing unit comprises a graphene layer. The method for forming the biosensor that comprises at least one sensor comprising a sensing unit, a bridge unit connected to the sensing unit and an electrode unit connected to the bridge unit, comprises forming a lower insulation layer, forming a conductive electrode layer on the lower insulation layer, forming a graphene layer on the conductive electrode layer and forming a reaction layer on the graphene layer.

Abstract: Methods, system and devices for monitoring a plurality of parameters associated with a closed loop control operation including continuously monitoring a physiological condition and automatic administration of a medication, detecting an adverse condition associated with the monitored physiological condition or the medication administration deviating from a predetermined safety level of the closed loop control operation, and initiating a non-zero pre-programmed medication delivery rate are provided.

Abstract: An automatic administration instrument includes a syringe and a partition wall in the syringe which partitions the syringe into different rooms for respectively holding plural kinds of drug solutions or a drug and a drug solution. A partition-wall driver displaces the partition wall and an injection needle is connected to the syringe. A body cap attached to the administration instrument body so as to cover the injection needle. The syringe, the partition wall, and the body cap are configured such that displacing the partition wall dissolves or mixes the drug solutions or the drug and the drug solution in a state that the injection needle is covered by the body cap.

Abstract: An automatic administration instrument includes a syringe and a partition wall in the syringe which partitions the syringe into different rooms for respectively holding plural kinds of drug solutions or a drug and a drug solution. A partition-wall driver displaces the partition wall and an injection needle is connected to the syringe. A body cap attached to the administration instrument body so as to cover the injection needle. The syringe, the partition wall, and the body cap are configured such that displacing the partition wall dissolves or mixes the drug solutions or the drug and the drug solution in a state that the injection needle is covered by the body cap.

Abstract: An automatic administration instrument includes a syringe and a partition wall in the syringe which partitions the syringe into different rooms for respectively holding plural kinds of drug solutions or a drug and a drug solution. A partition-wall driver displaces the partition wall and an injection needle is connected to the syringe. A body cap attached to the administration instrument body so as to cover the injection needle. The syringe, the partition wall, and the body cap are configured such that displacing the partition wall dissolves or mixes the drug solutions or the drug and the drug solution in a state that the injection needle is covered by the body cap.

Abstract: An automatic administration instrument includes a syringe and a partition wall in the syringe which partitions the syringe into different rooms for respectively holding plural kinds of drug solutions or a drug and a drug solution. A partition-wall driver displaces the partition wall and an injection needle is connected to the syringe. A body cap attached to the administration instrument body so as to cover the injection needle. The syringe, the partition wall, and the body cap are configured such that displacing the partition wall dissolves or mixes the drug solutions or the drug and the drug solution in a state that the injection needle is covered by the body cap.

Abstract: An automatic administration instrument includes a syringe and a partition wall in the syringe which partitions the syringe into different rooms for respectively holding plural kinds of drug solutions or a drug and a drug solution. A partition-wall driver displaces the partition wall and an injection needle is connected to the syringe. A body cap attached to the administration instrument body so as to cover the injection needle. The syringe, the partition wall, and the body cap are configured such that displacing the partition wall dissolves or mixes the drug solutions or the drug and the drug solution in a state that the injection needle is covered by the body cap.

Abstract: An automatic administration instrument includes a syringe and a partition wall in the syringe which partitions the syringe into different rooms for respectively holding plural kinds of drug solutions or a drug and a drug solution. A partition-wall driver displaces the partition wall and an injection needle is connected to the syringe. A body cap attached to the administration instrument body so as to cover the injection needle. The syringe, the partition wall, and the body cap are configured such that displacing the partition wall dissolves or mixes the drug solutions or the drug and the drug solution in a state that the injection needle is covered by the body cap.

Abstract: An autoinjector having a body (1) adapted to receive a reservoir containing fluid and including a piston (P) and a needle. The body (1) has a distal portion, a middle portion, and a proximal portion, the middle portion including at least one middle window (12) making it possible, before use, to see 100% of the fluid contained in the reservoir and, after injection, to see the piston (P). The middle window (12) has an external shape of an arrow that points towards the proximal portion. The proximal portion (121) of the middle window (12) includes a triangular end portion, forming the point of the arrow, the base of the triangular end portion, remote from the point, forms the widest portion of the middle window (12).

Abstract: The present invention relates to an injection device. The injection device comprises a body (11) for holding a syringe that has a needle (17) at one end and a cap (21) that is removably attached to the body. The cap (21) has a needle shield to cover said needle. The injection device further comprises a gear assembly comprising a first rotary gear (29) and a first linear gear (28) to engage with the first rotary gear. The gear assembly is configured such that rotation of the first rotary gear drives the first linear gear to urge the needle shield away from the body. An actuator is provided that is configured to rotate the first rotary gear.

Abstract: Apparatus configured to assist a user in correctly positioning the apparatus on a drug delivery device, the apparatus comprising: attachment means for attaching the apparatus to the drug delivery device; an imaging arrangement for capturing at least one image of a portion of a delivery device; a processor for processing the captured at least one image to determine a position of the apparatus relative to the drug delivery device and to determine a manner in which the apparatus should be moved in order to correctly position the apparatus on the drug delivery device; and a display for displaying an indication of the manner in which the apparatus should be moved in order to correctly position the apparatus on the drug delivery device.

Abstract: A medicament injection device comprising a main body configured to receive a medicament cartridge sealed by a penetrable barrier; a cap assembly having an inner needle part and an outer needle part, wherein the inner needle part is movable in a proximal direction with respect to the outer needle part, a needle carrier carrying a needle, the needle carrier being releasably coupled to the inner needle part, wherein, when the inner needle part is displaced in the proximal direction, the inner needle part causes the needle carrier to be displaced axially in the proximal direction; and wherein, subsequent to the axial displacement of the inner needle part, the cap assembly is separable from the main body by movement of the cap assembly in a distal direction.

Abstract: An injection device comprises a housing containing a cartridge, a needle holder including an injection needle, and a cap. The cap is removably engaged with the housing. The injection device also comprises a translating mechanism configured such that linear distal movement of the cap causes proximal movement of the needle holder such that the injection needle pierces the cartridge.

Abstract: An auto-injector for delivering a liquid medicament comprising: a housing arranged to contain a syringe and a piston for sealing the syringe and displacing the medicament, the housing having a proximal end and a distal end intended to be applied against an injection site, wherein the syringe comprises: a plurality of plunger elements arranged along a length of the syringe between the proximal end of the housing and the piston, each of the plurality of plunger elements having a longitudinal axis; and a cord arranged to connect the plurality of plunger elements, wherein the plunger elements are configured to become aligned along their axes to push the piston towards the distal end to displace the medicament when the cord is acted on by a driving force.

Abstract: Systems, devices, and techniques are disclosed for administering and tracking medicine to patients and providing health management capabilities for patients and caregivers. In some aspects, a system includes an injection pen device including a dose setting mechanism, a dispensing mechanism, and an electronics unit to generate dose data associated with a dispensing event of a dose of the medicine dispensed from the injection pen device and time data associated with the dispensing event; a mobile device in wireless communication to receive and process the dose data; and a software application configured to determine a recommended dose based on health data and contextual data associated with a user of the injection pen device, the software application including a learning dose calculator module to adaptively calculate the recommended dose of the medicine based on time-relevant and circumstances-relevant data specific to the user of the injection pen device.

Abstract: A supplementary device is configured to be attached to a drug delivery device. The supplementary device comprises a non-contact sensor configured to output signals indicative of the position of a moveable component within the drug delivery device. The supplementary device further comprises a processor configured to receive the signals output from the non-contact sensor. This processor is additionally configured to determine, based on the signals, whether the drug delivery device is in a pre-activation state or a post-activation state.

Abstract: The present disclosure relates to a medicament delivery device (1) comprising: a main housing (3) arranged to accommodate a medicament container, an activation button (5) linearly displaceable from a first position relative to the main housing (3) to a second position, whereby a medicament administration procedure for expulsion of medicament from the medicament container is initiated, a first sensor (15) arranged to detect a medicament administration procedure initiated by the activation button (5), a storage unit (19) containing remaining dose data, and processing circuitry configured to update the remaining dose data based on detection of a medicament administration procedure by the first sensor (15), wherein the medicament delivery device (1) is arranged to enable presentation of the remaining dose data.

Abstract: A syringe assembly includes a housing having a cavity for receiving an associated fluid. A plunger assembly includes a piston and a shaft connected thereto for selectively dispensing the associated fluid from the housing through a dispensing opening. A container receives the housing and plunger assembly. The container has a first opening at a first end that selectively receives a cap thereon and covers the dispensing opening when the cap is secured to the container, and second opening at a second end that opens to the plunger assembly shaft.

Abstract: The present invention relates to a pen injecting device for delivering a liquid medicament comprising a pen body, a needle received in a first end of the pen body, an inner needle shield removeably located over the needle to enclose the needle, an outer needle shield removeably located over the inner needle shield to enclose the inner needle shield and a pen cap removeably attached to the first end of the pen body so as to enclose the outer needle shield. The pen cap comprises an arm depending from an inside surface of the cap and extending away from the first end of the pen body toward the inner and outer needle shields, the arm having a sharp end so that, as the cap is removed from the body, the sharp end of the arm grips the inner or outer needle shield to retain it in the cap and expose the needle.

Abstract: An auto-injector device comprises a cap removal mechanism which comprises a retractable component which is slidably mounted within a housing of the device, and a cap-removal actuator to push the retractable component out of the housing to remove a cap from the device; a dispense mechanism which comprises a driving element to expel a medicament from the device; and a dispense button which activates the cap removal mechanism when pressed a first time, engages with the dispense mechanism when released, and activates the dispense mechanism when pressed a second time. The dispense mechanism comprises an engaging element configured to engage with the dispense button when the dispense button has been pressed for a first time and released.

Abstract: A medicament injection device includes a main body having a cartridge receiving part configured to hold a medicament cartridge; a needle holder holding a needle; a needle sleeve at least partially surrounding the needle holder and needle and axially movable relative to the main body; a removable transverse blocking member separating the cartridge receiving part and the needle holder; and a compressed spring arranged between the needle holder and a distal end of the needle sleeve so that, upon removal of the blocking member, the spring is released, thereby causing the needle carrier to move axially towards cartridge receiving part.

Abstract: A medicament delivery device is presented having a medicament container having an attached medicament delivery member; a housing where the medicament container is movable between a retracted and an extended position in which the medicament delivery member extends from the housing; a drive unit that advances the medicament container from its retracted position to its extended position to expel the contents through the medicament delivery member; and a medicament container holder for carrying the medicament container as it is advanced, the medicament container holder having a proximal end through which the medicament delivery member extends and a holding member releasably connected to the drive unit and attached to the medicament container holder.

Abstract: The present invention relates to an injector for preventing accidental needle sticks comprising:—a cylinder extending along a longitudinal axis, an inner wall and an outer wall, the cylinder having an outlet at an outlet end opposite an actuating end and a finger grip on the outer wall, which finger grip is positioned between the outlet end and the actuating end,—a piston having a piston body and a deformable sealing element, which deformable sealing element abuts the inner wall of the cylinder at an abutting interface and seals an annular gap between the piston body and the inner wall of the cylinder when the piston is inserted in the cylinder,—a needle guard for mounting on the outside of the cylinder from the outlet end or the actuating end, which needle guard comprises a barrel with a mounting end opposite an operating end, the barrel having a slot for receiving the finger grip of the cylinder when the needle guard is mounted on the cylinder, which slot extends from the mounting end towards the operating

Abstract: A syringe needle shield includes a first part and a second part. The first part is connected to the second part by a pivotable first connection portion. The second part is pivotable on the first connection portion toward the first part, and a needle hob is clamped between the first and second parts. The first and second parts are securely connected to each other by the first snapping portion which cannot be unlocked from each other. The first part is connected to a needle shield by a flexible plate. The shield receives a push force from its back so as to move from a first position to a second position. When the shield is located at the second position, a restriction portion is fixedly engaged with an engaging portion.

Abstract: An injection device comprising: a housing arranged to contain a medicament cartridge; a needle holder holding an injection needle; a generally tubular needle sleeve fixed with respect to the needle holder and axially movable with respect to the housing; and a gear assembly comprising a rotary gear fixed to the needle holder, a first gear rack disposed on the needle sleeve and a second gear rack disposed on the housing, wherein the gear assembly is arranged so that movement of the needle sleeve in a proximal axial direction causes movement of the needle holder in the proximal axial direction.

Abstract: A medicament injection device comprising: a main body configured to receive a medicament cartridge, a needle sleeve axially movable with respect to the main body, a needle holder holding a needle, and a displacement element coupled to the needle holder and disengageably coupled to the needle sleeve; wherein, upon axial displacement of the needle sleeve by a predefined distance in a proximal direction, the needle carrier and needle are displaced axially in a proximal direction.

Abstract: The present disclosure illustrates a protective sleeve for a syringe. The protective sleeve includes a hollow pipe body and an outer sleeve. The pipe body includes a channel passing therethrough axially, and a connection part formed at a side thereof and configured to combine with the preset syringe. The outer sleeve is movably and extendably mounted on the pipe body. A hollow body of the outer sleeve includes a through hole passing through axially and configured for insertion of the pipe body, and a covering part formed at an end thereof. After the syringe is injected already, the outer sleeve can be extended outwardly to make the covering part completely cover a needle of the syringe, thereby preventing the needle from being exposed out of the outer sleeve to stab person. As a result, the protective sleeve of the present can improve safety in using syringe.

Abstract: There is provided a protected needle assembly. The assembly includes an outer barrel receiving a needle therethrough. The assembly includes an inner barrel resiliently biased to extend about the needle in a protected needle mode. The inner barrel is retractable into the outer barrel in a first instance to deploy the needle. The assembly includes a locking mechanism actuated upon the inner barrel moving towards the protected needle mode once more. The locking mechanism is configured to inhibit further retraction of the inner barrel thereafter.

Abstract: A needle assembly has a needle hub that has a body to which are formed two plates at opposite sides thereof in a parallel relationship. The plates have respective upper edges and lower edges that lie substantially along respective planes, so that the needle hub may be stably placed onto a surface by means of the respective edges. A partition is formed orthogonally proximate to the front ends of the parallel plates. The partition and the parallel plates together provide upper and lower three point stable supports for the needle hub. A notch at the partition provides a guided line of sight to the tip of the needle for the user. The connector at the proximal portion of the needle hub has a non-conventional configuration that allows it to mate only with a counterpart special connector of a fluid conveying device that has a complementary non-conventional configuration.

Abstract: A needle house (115) having a distal end which is removably connected to a source of injectable fluid (110) and a proximal end (80) for contacting a patient, as well as to an injection apparatus comprising the needle housing. The needle housing comprises a) a hollow needle through which the injectable fluid is deliverable to the patient, the needle having a proximal end for insertion into body tissue of the patient, and (b) a chamber (75) having an open proximal end, the chamber surrounding at least part of the needle and extending proximally beyond the proximal end of the needle to the open proximal end. The open proximal end of the chamber is deformable and is moveable relative to the needle from a position in which the chamber extends proximally beyond the proximal end of the needle to a position in which the proximal end of the needle extends proximally through the open proximal end of the chamber.