121 results about "Disposable Needle" patented technology

A needle assembly including a cover, an inner shield, a needle and a hub assembly is provided. After use, the cover is placed over the distal (patient) end of the needle and the inner shield can be used to cover the proximal (non-patient) end of the needle. The inner shield comprises flexible extensions above its open end to secure the inner shield over the proximal end of a needle in the needle assembly. A needle hub is also provided that eliminates adhesive bumps at the base of the needle and further distributes needle angular bending along an irregular surface, which facilitates proper insertion technique and effective needle length. The hub further includes stanchions or castellations on its edge such that when the patient uses proper injection techniques, the edges of the hub leave a distinctive impression in the skin of a user for a short period of time.

A needle assembly that has a flexible shield movable between (i) a first position, where the flexible shield is uncompressed, and (ii) a second position, where the flexible shield is compressed and an administering member located within the flexible shield, where at least one of the administering member and the flexible shield is axially movable with respect to the other of the administering member and the flexible shield in an unlocked position prior to and during usage of the needle assembly, and the at least one of the administering member and the flexible shield is no longer axially movable with respect to the other of the administering member and the flexible shield in a locked position. Prior, during and after use of the needle assembly, the needle is never exposed. After a single usage of the needle assembly, the needle is locked within the flexible shield and cannot be reused.

In an aspect, a medication delivering injector which includes a housing having opposing proximal and distal ends and an accessible internal cavity for inserting and removing a medicament container such as a syringe. The injector is designed to hold and manipulate a medication delivery device such as a large variety of standard and non-standard medical syringes with fixed or attached needles, assembled such that centrally located is a cylinder containing a liquid medicament and attached either permanently or removably to the distal end of the cylinder, is a hypodermic needle or cannula in fluidic communication with the cylinder. The needle can be from one-half inches to one-and-one-half inches in length in the illustrated embodiment and other sizes are possible by changes in scale of the injector. At the proximal end of the cylinder is an opening with an inserted seal or bung with an attached rod thus constituting a plunger. The central medicament containing cylinder could also be a standard medicament cartridge. Hereinafter, both are referred to as a “syringe”. A lid or access cover which, in an open position permits insertion and removal of the syringe into / from the housing in a horizontal fashion thus providing ease of loading. The syringe is inserted with the needle end toward the distal end of the housing and the plunger toward the proximal end of the housing. A movable carriage is disposed in the proximal end of the housing and slides in the axial direction forwards and rearwards such that a syringe, whose proximal end is gripped by the carriage, so moves with the carriage such that the needle exits the housing at the distal end of the housing and pierces the tissue of the patient prior to dispensing of the medicament, and then is retracted after the medicament has been dispensed by retraction of the carriage. Attached to the carriage is an actuator which pushes on the syringe plunger causing the medicament contained within the syringe cylinder to be dispensed through the needle into the patient's tissue. In one embodiment suitable for both removable needle and fixed needle syringes, the proximal end of the syringe including the syringe finger flange is gripped by an elastomeric flange grip which resides within the carriage, while the syringe distal end resides in and is supported by a “syringe guide” which is attached to the carriage and thus moved with it. In another embodiment which is so made to accommodate syringes with removable needles and their safe disposal, the syringe flange at the proximal end of the cylinder is gripped by an elastomeric flange grip which resides in the carriage as described above, while the syringe distal end is supported by a needle which resides in a removable disposable needle shield. The needle guide is biased toward the carriage and thus, the syringe body is compressed and guided as the carriage moves forward and rearward.Both the movement of the carriage and the actuator are controlled by servo motors which are controlled by electronics and a microcontroller so operating such that speeds and accelerations are controlled smoothly and gently so as to avoid the stop / start motion of motors controlled by limit switches and simple electronics or the vibration and abruptness such as result from injectors powered by compressed springs or gas. Furthermore, the forces are adaptive to the loads imposed and the requirements necessary for the proper dispensation of medicaments with high viscosity or sensitivity to shear forces.The housing, approximately midway between proximal and distal ends, is affixed by a hinge such that the device can be folded in half to provide for a more compact device to be stored and transported.On the distal end of the housing are electrical sensor pads in communication with the microcontroller such that contact with the patient's skin and the angle at which the injector is held against the skin and the steadiness with which the injector is being held can be ascertained. Within the housing are a haptic vibrator and an audio speaker, both producing a vibration which is variable in pitch in such a manner that biofeedback is provided to the injector user as to the pressure, angle and steadiness with which they are holding the injector against the skin. This facilitates the action of injection oneself in the gluteus muscle where visual feedback isn't available to the patient.Multiplexed onto the electrical sensor pads, is a TENS (Transcutaneous Electrical Nerve Stimulation) generator which is operational (at the user's choice) just before and during the injection to interrupt or quench the pain of tissue perforation often accompanied with needle injections.Contained on the surface of the housing such as on the access cover, is a display such that user menus, device state, directions, and battery charge status, etc. are displayed. Also contained on the surface of the housing, on the proximal half, are buttons which control the menus and selections that are shown on the display. These selections provide for the user to set such parameters as hypodermic insertion speed and medicament dispensing speeds, the preferred mode of user biofeedback which can include: speech mode (which can be accompanied by musical themes and ringtones, plus variable pitch tone and haptic vibration), MP3 mode (which has speech muted but includes musical ringtones and variable pitch tone and haptic vibration), and haptic mode (which is haptic vibration and audio tone queues needed for injector position biofeedback and readiness), plus mute mode (which provides no audio but the haptic vibration remains), and none, which provides no vibrational biofeedback, yet the display information always remains available.Also contained on the surface of the housing on the distal half, is an “injection initiate” button which causes the sequences required for performance of an injection to occur if said button is “enabled”.Contained within the electronics and its operating program is the ability to audibly play pre-recorded human speech in any language such that: directions in the form of consecutive steps which are required to load the medicament container (syringe) into the device, consecutive steps to perform an injection, steps to remove and properly dispose of parts, to alert of device status and menu choices, etc. can be played through the audio speaker. Also contained within the electronics and program is the ability to play musical ringtones as a distraction during the needle insertion and injection or when a scheduled injection alarm is reached, or calming human voice exhibiting bedside manner during the needle insertion and injection.Also contained within the electronics and software is a real-time clock-calendar which can store a patient's injection schedule and play a musical ringtone as an alarm as each scheduled injection becomes due. Also contained within the electronics and software are the ability to communicate with a personal computer through a USB port, which can also charge the injector's rechargeable battery. The battery in one embodiment, consists of three AAA batteries which can be rechargeable or non-rechargeable. The USB port in combination with an application running on the personal computer, is used to download the injection schedule into the real-time clock-calendar and to download ringtones and musical themes of the user's choice and to download foreign language sets for the pre-recorded human language feature.The injector can be further equipped with the capability to aspirate the tissue by drawing back on the plunger thus creating a vacuum into which fluids will flow. These fluids enter the syringe cylinder where they can be checked for the presence of blood by optical absorption in the red spectrum. This information is useful in the instances where intramuscular injections are to be given with drugs whose ‘Full Prescribing Information’ instructs the patient to aspirate and check for blood in the syringe which indicates that the puncture of a vein has occurred, and if so detected, to abort the injection and then re-inject into a different location.

A single-use needle cover configured to obscure, protect, or hide at least a portion of a needle from view before, during, and / or after an injection and / or aspiration procedure is disclosed. In some embodiments, the cover includes a housing at least partially containing the needle and configured to couple to a syringe, wherein the housing includes an axis and a guide member. In some embodiments, a sleeve has a plurality of tracks configured to slidingly receive the guide member, wherein the sleeve is configured to retract, extend, and rotate with respect to the housing. In some embodiments, after the sleeve has been retracted and extended one time, a first locking member inhibits further retraction of the sleeve and a second locking member inhibits rotation of the sleeve.

A single use needle-like probe contains optical fibers to deliver and collect light at the distal tip of the needle-like probe. The single use needle-like probe may connect to a handpiece that may contain sensors to monitor how the probe is being used. Sensors within the handpiece may, e.g., include a force sensor and a position sensor that detect the depth of the probe in tissue. The handpiece may be connected through a cable to a control unit that may include light sources, optical detectors, control electronics and one or more microprocessors to analyze the data collected.

The invention discloses a disposable adjustable injection device for insulin injection. The device comprises a protection cover, a disposable syringe needle, an injection refill sleeve, a main deviceshell, an injection refill and an adjusting assembly, a second boss is arranged at one end of the main device shell, and the injection refill sleeve is installed on the outer portion of the second boss; a threaded groove is formed in one end of the injection refill sleeve, an outer thread of the second boss is in mutual threaded connection with the threaded groove, and a first boss is arranged atthe other end of the injection refill sleeve; the outer portion of the first boss is in threaded connection with the disposable syringe needle, a steel needle is inserted in the disposable syringe needle, and the injection refill is installed in the injection refill sleeve; the protection cover sleeves the outer portion of the injection refill sleeve, the adjusting assembly is arranged at the other end of the main device body shell, a fixed sleeve is installed in the main device body shell, and one end of the fixed sleeve protrudes outward to form a flange part. The device has the advantages that the operation is simple, the waste is avoided, and the safety performance is good.

A needle dispensing system including a pen-type hypodermic syringe having a threaded end that is suitable for mating with a needle assembly having a threaded portion that is complementary to the threaded end of the syringe and located within a closed pod. A hand tool is provided for controlling the pod that includes a collet sized so as to releasably grip a portion of the closed pod for opening. The hand tool also includes a radiused guard that helps to prevent inadvertent needle sticks during use, and a biased release button the actuation of which causes the opened pod to be released from the collet. A hand tool is also provided for controlling a container holding a disposable needle assembly that includes a housing that supports a collet that is sized so as to releasably grip a portion of the container for opening, and a biased release button the actuation of which causes the opened pod to be released from the collet.

A transabdominal needle introducer for the repair of large ventral incisional hernias comprises a handle connected to a long tubular shaft and a disposable needle cartridge at its distal end. The handle has a round knob or head, and a needle pusher to extrude the needles out. The long tubular shaft contains two metal rods disposed inside thereof, one to change the angle of the cartridge, and the other one to extrude the needles. At the proximal end of the tubular shaft there is a rotatable cylindrical control provided with a spiral groove that moves a metal rod destined to pivot the needle cartridge. The second metal rod inside the shaft is assigned to extrude the needles and is connected to a flexible resilient wire that protrudes at the distal end of the tubular shaft and is provided at its distal end with an oval tip that engages a piston-type pusher inside the needle cartridge. There are two straight needles inside the cartridge that are attached to a single strand of suture at each end, and they can be extruded by action of the needle pusher.

A single-use needle cover configured to obscure, protect, or hide at least a portion of a needle from view before, during, and / or after an injection and / or aspiration procedure is disclosed. In some embodiments, the cover includes a housing at least partially containing the needle and configured to couple to a syringe, wherein the housing includes an axis and a guide member. In some embodiments, a sleeve has a plurality of tracks configured to slidingly receive the guide member, wherein the sleeve is configured to retract, extend, and rotate with respect to the housing. In some embodiments, after the sleeve has been retracted and extended one time, a first locking member inhibits further retraction of the sleeve and a second locking member inhibits rotation of the sleeve.

A method of removing lesions by implanting a radioactive seed at the location of the lesion, locating the lesion with the radioactive seed, and removing the lesion with the radioactive seed. A kit is also provided by the present invention for use in removing lesions by implanting a radioactive seed at the location of the lesion, locating the lesion with the radioactive seed, and removing the lesion with the radioactive seed. Other embodiments of the invention include: a disposable needle preloaded with radioactive seed(s); and radioactive seeds comprising hooks to ensure proper localization of the seed(s) in the patient.

A needle assembly including a cover, an inner shield, a needle and a hub assembly is provided. After use, the cover is placed over the distal (patient) end of the needle and the inner shield can be used to cover the proximal (non-patient) end of the needle. The inner shield comprises flexible extensions above its open end to secure the inner shield over the proximal end of a needle in the needle assembly. A needle hub is also provided that eliminates adhesive bumps at the base of the needle and further distributes needle angular bending along an irregular surface, which facilitates proper insertion technique and effective needle length. The hub further includes stanchions or castellations on its edge such that when the patient uses proper injection techniques, the edges of the hub leave a distinctive impression in the skin of a user for a short period of time.

The invention provides a description of a method and a device suitable for producing a cell suspension spray with living cells, and the produced cell preparation, suitable for grafting to a patient. In contrast to other methods, the spraying is performed through a disposable needle which is inserted into a disposable air tube; which provides a cell distribution avoiding spray nozzles. Small suspension droplets are provided instead of cell nebulization. By using medical grade sterile Luer-lock disposables from medical routine praxis, biocompatibility and easy application is addressed. In applying the method and / or in using the device, cells suitable for grafting to a patient are dispersed in a solution and sprayed with the device for distribution over the recipient graft site.

A transabdominal needle introducer for the repair of large ventral incisional hernias comprises a handle connected to a long tubular shaft and a disposable needle cartridge at its distal end. The handle has a round knob or head, and a needle pusher to extrude the needles out. The long tubular shaft contains two metal rods disposed inside thereof, one to change the angle of the cartridge, and the other one to extrude the needles. At the proximal end of the tubular shaft there is a rotatable cylindrical control provided with a spiral groove that moves a metal rod destined to pivot the needle cartridge. The second metal rod inside the shaft is assigned to extrude the needles and is connected to a flexible resilient wire that protrudes at the distal end of the tubular shaft and is provided at its distal end with an oval tip that engages a piston-type pusher inside the needle cartridge. There are two straight needles inside the cartridge that are attached to a single strand of suture at each end, and they can be extruded by action of the needle pusher.

A disposable needle hair transplanter includes: a plunger structure having an outer barrel defining a passage, a plunger assembly having at least one push needle movable within the passage of the outer barrel, and a hair transplantation depth controller drivingly connected with the plunger assembly via a link; a needle having a needle seat connected with the outer barrel and at least one needle tube in which a hair follicle is loadable, the hair transplantation depth controller serving to restrict the depth by which the needle tube is thrust into the scalp; and a hair follicle depth controller having a cylindrical structure fitted around the needle seat and a shaft tube connected with the cylindrical structure and coaxially disposed around the needle tube. The hair transplantation depth controller is disposed around the shaft tube and movable along the shaft tube toward or away from the scalp.

The invention discloses a method for measuring trace chloridion and sulfate radical in loprazolam samples by ion chromatography and belongs to the field of analytic chemistry. The method includes the followings steps of preparing and analyzing Cl- and SO42- mixed standard solution and obtaining a linear equation of concentration and peak area, pretreating the loprazolam samples, feeding the treated loprazolam samples to an ion chromatography by a disposable needle type filter, utilizing 3.6mmol / L sodium carbonate as leacheate and analyzing and measuring the content of the chlorodion and the sulfate radical according to the obtained linear equation, wherein a chromatographic column adopted in the ion chromatography is a high-capacity chromatographic column, the inner diameter of filler of the chromatographic column is 5 micrometers, the temperature of a column temperature box is set to be 45 DEG C, sampling input quantity is 100 microliters, applied curb current is 40mA, and flow velocity is 0.8ml / min. The method is quick and simple, high in accuracy, convenient and easy to operate and applicable to quality control in the process of production of loprazolam, the integral analyzing process can be completed within 25min, and the detection requirements of the fine chemical industry are met.

A semi-automatic “fixed” dose injection device is disclosed containing a reservoir of medicament, where a trigger controls the unwinding of a torsional spring to cause a predetermined injection of medicament from the reservoir through a disposable needle.

Needles are widely used in interventional radiology. Each medical application requires a specific needle type. The same holds for the photonic needles which analysis depends on the type of application the clinician aims for. Therefore, it is relevant to have the X-ray machine recognize the type of needle that is being used and to load the required software for the tissue analysis. It is therefore proposed to have a data link established between the imaging modality used for the acquisition of the patient anatomy (X-ray, CT, MR or US) and the system that processes optical data from the needle, so that the information from this imaging modality can be used to guide the processing. In a preferred embodiment the selection is made by reading out the code present in the disposable needle when it is connected to the console.

A tattooing apparatus for marking animals includes a “U” shaped pliers and a disposable needle carrier that contains plurality of needles that are arranged in desired patterns to be pressed onto animals tissue using tattoo ink. The needle carrier is made of one-piece molded part that can quickly connect into the opening of pliers handle by means of snug fit to be used for purpose of animal tattooing.

Disclosed is a disposable needle filter apparatus with a universal truncated syringe-receiving neck to enable the filtration of fluids / solutions aspirated into a needle-bearing syringe. The apparatus includes a needle seal stopper and needle stop to create a substantially airtight chamber to facilitate fluid aspiration through an enclosed filter and into the syringe. In an alternative embodiment, the filter apparatus includes an extended syringe-receiving neck configured to receive a specifically sized syringe / needle combination. In a further embodiment, the receiving neck is constructed as a modular unit to allow for interchangeable necks to accommodate different needle and syringe sizes with different cross-sectional diameters. In a yet further embodiment, the neck is constructed with stepped tapered segments of serially larger cross-sectional diameters to accommodate differently sized syringes. In a still further embodiment, the apparatus includes an accessory needle secured to the apparatus inlet.

The invention discloses a wart cutting device for the dermatology department and relates to the technical field of medical equipment. The device comprises a thin rod, two cutter bodies are rotatably and symmetrically arranged on the upper portion of the surface of the thin rod, and a sleeve is arranged on the upper portion of the surface of the thin rod and located below the cutter bodies; a push-pull device is arranged at the bottom of the left side of the outer wall of the thin rod, a half frame is welded to the bottom of the right side of the outer wall of the thin rod, and a mobile rod isslidingly inserted in an inner cavity of the sleeve; the top of the mobile rod is rotatably connected with the two cutter bodies, a pull ring is welded to the bottom of the mobile rod and clamped by using U-shaped clamping plates, limit bolts and check pawls are alternately and tightly screwed and separated from ratchet wheels, coiling cylinders are rotated, nylon ropes, clamping discs and limit screws are used for clamping a piston rod of a disposable needle tubing to move, and medical spraying for hemostasis and wart residue suction are completed. The wart cutting device is convenient to use, replace, disassemble, assemble and sterilize and high in practicability.

A disposable needle for syringes and infusions includes a tubular needle body (1), one end of which consists of a pyramid needle tip (2), a conical needle tip (4) or the combination of a pyramid needle tip and a conical needle tip, a through-hole (3) communicating with the inner hole of the needle body (1) is provided on the tubular needle body (1) and the conical needle tip (4), or on the other part. The said conical needle tip (4) is solid, hollow or locally hollow. A manufacture of the said needle is also provided.

Provided is a blood collecting pen. The blood collecting pen is a shell which comprises a pen holder, a back cover, buttons and an adjusting device, and the shell is internally provided with a blood collecting device, a needle retreating device and a disposable needle; the blood collecting pen is characterized in that the disposable needle is directly inserted into a needle sleeve so as to lock the blood collecting device and the needle retreating device, a protective cap is unscrewed, and a blood collecting button is pushed once so as to unlock the blood collecting device; the needle quickly penetrates into skin so as to complete blood collection, wherein the depth of penetration into the skin is adjusted by the adjusting device, and then a needle retreating button is pushed once so as to unlock the needle retreating device; the disposable needle is taken out of the blood collecting pen so that an entire blood collection procedure can be completed, or a holder retreating needle is pushed so as to directly drive the needle out of the blood collecting pen, so that the blood collection procedure is completed.

The invention relates to a disposable syringe medical treatment apparatus. The disposable syringe medical treatment apparatus comprises a main box, a needle cylinder separating device and a needle head cutting device, the needle cylinder separating device is installed at the upper end of the main box, and the needle head cutting device is installed at the rear end of the main box. The disposable syringe medical treatment apparatus can solve the problems that by means of an existing damaging type syringe, a needle cylinder needs to be manually separated from a needle head, then the needle headis pinched off, when the syringe is separated, all parts need to be separated after the syringe is manually limited, when the needle head is separated, the chance is that the potential safety hazard is caused when the hand is punctured by the needle head due to misoperation, the manual separating efficiency is low, a piston part in the needle cylinder needs to be manually taken out, since the needle cylinder is small in size, manual separation is not easy, when the needle head is pinched off, since the needle head is fine and small, manual pinch-off is not easy, the time consumed in the process is long, the labor intensity is large, and the efficiency is low; the functions of targetedly separating a disposable needle cylinder and cutting the needle head can be achieved.

A method of removing lesions by implanting a radioactive seed at the location of the lesion, locating the lesion with the radioactive seed, and removing the lesion with the radioactive seed. A kit is also provided by the present invention for use in removing lesions by implanting a radioactive seed at the location of the lesion, locating the lesion with the radioactive seed, and removing the lesion with the radioactive seed. Other embodiments of the invention include: a disposable needle preloaded with radioactive seed(s); and radioactive seeds comprising hooks to ensure proper localization of the seed(s) in the patient.

In an aspect, a medication delivering injector which includes a housing having opposing proximal and distal ends and an accessible internal cavity for inserting and removing a medicament container such as a syringe. The injector is designed to hold and manipulate a medication delivery device such as a large variety of standard and non-standard medical syringes with fixed or attached needles, assembled such that centrally located is a cylinder containing a liquid medicament and attached either permanently or removably to the distal end of the cylinder, is a hypodermic needle or cannula in fluidic communication with the cylinder. The needle can be from one-half inches to one-and-one-half inches in length in the illustrated embodiment and other sizes are possible by changes in scale of the injector. At the proximal end of the cylinder is an opening with an inserted seal or bung with an attached rod thus constituting a plunger. The central medicament containing cylinder could also be a standard medicament cartridge. Hereinafter, both are referred to as a “syringe”. A lid or access cover which, in an open position permits insertion and removal of the syringe into / from the housing in a horizontal fashion thus providing ease of loading. The syringe is inserted with the needle end toward the distal end of the housing and the plunger toward the proximal end of the housing. A movable carriage is disposed in the proximal end of the housing and slides in the axial direction forwards and rearwards such that a syringe, whose proximal end is gripped by the carriage, so moves with the carriage such that the needle exits the housing at the distal end of the housing and pierces the tissue of the patient prior to dispensing of the medicament, and then is retracted after the medicament has been dispensed by retraction of the carriage. Attached to the carriage is an actuator which pushes on the syringe plunger causing the medicament contained within the syringe cylinder to be dispensed through the needle into the patient's tissue. In one embodiment suitable for both removable needle and fixed needle syringes, the proximal end of the syringe including the syringe finger flange is gripped by an elastomeric flange grip which resides within the carriage, while the syringe distal end resides in and is supported by a “syringe guide” which is attached to the carriage and thus moved with it. In another embodiment which is so made to accommodate syringes with removable needles and their safe disposal, the syringe flange at the proximal end of the cylinder is gripped by an elastomeric flange grip which resides in the carriage as described above, while the syringe distal end is supported by a needle which resides in a removable disposable needle shield. The needle guide is biased toward the carriage and thus, the syringe body is compressed and guided as the carriage moves forward and rearward.Both the movement of the carriage and the actuator are controlled by servo motors which are controlled by electronics and a microcontroller so operating such that speeds and accelerations are controlled smoothly and gently so as to avoid the stop / start motion of motors controlled by limit switches and simple electronics or the vibration and abruptness such as result from injectors powered by compressed springs or gas. Furthermore, the forces are adaptive to the loads imposed and the requirements necessary for the proper dispensation of medicaments with high viscosity or sensitivity to shear forces.The housing, approximately midway between proximal and distal ends, is affixed by a hinge such that the device can be folded in half to provide for a more compact device to be stored and transported.On the distal end of the housing are electrical sensor pads in communication with the microcontroller such that contact with the patient's skin and the angle at which the injector is held against the skin and the steadiness with which the injector is being held can be ascertained. Within the housing are a haptic vibrator and an audio speaker, both producing a vibration which is variable in pitch in such a manner that biofeedback is provided to the injector user as to the pressure, angle and steadiness with which they are holding the injector against the skin. This facilitates the action of injection oneself in the gluteus muscle where visual feedback isn't available to the patient.Multiplexed onto the electrical sensor pads, is a TENS (Transcutaneous Electrical Nerve Stimulation) generator which is operational (at the user's choice) just before and during the injection to interrupt or quench the pain of tissue perforation often accompanied with needle injections.Contained on the surface of the housing such as on the access cover, is a display such that user menus, device state, directions, and battery charge status, etc. are displayed. Also contained on the surface of the housing, on the proximal half, are buttons which control the menus and selections that are shown on the display. These selections provide for the user to set such parameters as hypodermic insertion speed and medicament dispensing speeds, the preferred mode of user biofeedback which can include: speech mode (which can be accompanied by musical themes and ringtones, plus variable pitch tone and haptic vibration), MP3 mode (which has speech muted but includes musical ringtones and variable pitch tone and haptic vibration), and haptic mode (which is haptic vibration and audio tone queues needed for injector position biofeedback and readiness), plus mute mode (which provides no audio but the haptic vibration remains), and none, which provides no vibrational biofeedback, yet the display information always remains available.Also contained on the surface of the housing on the distal half, is an “injection initiate” button which causes the sequences required for performance of an injection to occur if said button is “enabled”.Contained within the electronics and its operating program is the ability to audibly play pre-recorded human speech in any language such that: directions in the form of consecutive steps which are required to load the medicament container (syringe) into the device, consecutive steps to perform an injection, steps to remove and properly dispose of parts, to alert of device status and menu choices, etc. can be played through the audio speaker. Also contained within the electronics and program is the ability to play musical ringtones as a distraction during the needle insertion and injection or when a scheduled injection alarm is reached, or calming human voice exhibiting bedside manner during the needle insertion and injection.Also contained within the electronics and software is a real-time clock-calendar which can store a patient's injection schedule and play a musical ringtone as an alarm as each scheduled injection becomes due. Also contained within the electronics and software are the ability to communicate with a personal computer through a USB port, which can also charge the injector's rechargeable battery. The battery in one embodiment, consists of three AAA batteries which can be rechargeable or non-rechargeable. The USB port in combination with an application running on the personal computer, is used to download the injection schedule into the real-time clock-calendar and to download ringtones and musical themes of the user's choice and to download foreign language sets for the pre-recorded human language feature.The injector can be further equipped with the capability to aspirate the tissue by drawing back on the plunger thus creating a vacuum into which fluids will flow. These fluids enter the syringe cylinder where they can be checked for the presence of blood by optical absorption in the red spectrum. This information is useful in the instances where intramuscular injections are to be given with drugs whose ‘Full Prescribing Information’ instructs the patient to aspirate and check for blood in the syringe which indicates that the puncture of a vein has occurred, and if so detected, to abort the injection and then re-inject into a different location.

An interconnect for connecting a needle electrode to a neurological testing device, the interconnect comprising: a needle-side connector and a device-side connector, wherein the needle-side connector and the device-side connector have complementary aspects so as to ensure that the correct needle electrode is used with a given neurological testing device.

A sticking agent for making a bacterial scanning electron microscope observation slice and a preparation method thereof are disclosed; every 100 ml of the sticking agent comprises 3-5mL of egg white, 5-7mL of glutinous rice powder emulsion, and balance of distilled water; the preparation method is as follows: respectively taking 3-5mL of the egg white and 5-7mL of the glutinous rice powder emulsion to put into a beaker, using sterile water to fix the volume to 100mL, evenly mixing, using a disposable needle filter with the specification of 0.22 mu m for filtering to obtain filtrate as the sticking agent; a method for making the scanning electron microscope bacterial ultramicroscopic morphology observation slice from the sticking agent comprises the steps of collection of bacteria, fixation, sticking, dehydration, replacement, critical point drying, sticking on a sample platform and ion sputtering; the effective sticking agent aiming at bacterial scanning electron microscope observation experiments and the preparation method thereof and a slice preparation method are provided, and the effective sticking agent solves slice shedding and mixing phenomena in the bacterial scanning electron microscope observation experiments.