Abstract: In a valve-equipped hand switch and a chemical liquid introduction system, a contrast medium in a syringe is delivered to a patient line through a first port, a main passage around a spacer portion, and a second port. Furthermore, a pressure (about 300 psi) of the contrast medium delivered by a chemical liquid introduction device is transmitted as a reaction force through a third plunger from a handle portion of an operation piston held by an operator. As such, the operator can directly feel the pressure of the introduced contrast medium, which gives a sense of ease to the operator during operation.

Abstract: A contrast liquid injector has a controller that calculates a necessary volume of the contrast medium based on a read out necessary dose of effective component per unit weight, weight of the subject, and concentration of the effective component. The injection rate of a base-operation condition is changed based on the calculated necessary volume of the contrast medium, wherein the predetermined injection time is unchanged, for all volumes of the contrast medium, when making the injection pattern, whereby a timing of an optimum concentration of the contrast medium will be substantially unchanged for all volumes of the contrast medium.

Abstract: The present invention relates to a finger-grip device designed to be placed on the flange of a cylindrical barrel of a medical syringe or cartridge, increasing the contact surface with the fingers of the operator during the injection or withdrawal of fluids to or from a patient, characterised in that it does not stop or hinder the run of the plunger within the cylindrical barrel.

Abstract: An absorbable sponge containing a contrasting agent (e.g, radiopaque agent) that can be introduced to a biopsy tract or other puncture wound site is provided. The contrasting agent permits identification of the site by fluoroscopy or other imaging techniques.

Abstract: A rotary medical manifold, for delivering various fluids through a patient delivery mechanism is described. The rotary manifold can include a manifold body and a valve stem. The manifold body can include a central cavity, an output port, a first fluid port, and a second fluid port. The valve stem can include an injector port, and a single central fluid passage. The valve stem can be adapted to slidably engage the central cavity of the manifold body and provide selective fluidic connectivity between the injector port and the output port, the first fluid port and the second fluid port.

Abstract: An injection device and methods for controlling the injection device are provided. Patient data for a patient to be treated are provided and an injection preparation (injectable) used in the injection device is automatically identified by the injection device automatically reading a label provided on a container of the injection preparation. Furthermore, contraindications for an identified injection preparation are determined. The patient data are compared with the any contraindication that has been determined At least one protective measure is adopted to prevent the injection when at least one contraindication matches the patient data. According to another variant of the method, patient data for a patient to be treated and contraindications for the injection preparations (injectables) available for a selection are established. The patient data are compared with the contraindications, wherein at least one injection preparation is suggested which contraindications do not match the patient data.

Abstract: A multi-dose injection system (108) is disclosed that allows for safe and easy use of bulk containers, a multi-use tubing set (110), and syringes (86a, 86b) across multiple patients. The bulk containers may include a saline bottle (118) and a contrast bottle (120) for administration to a series of patients undergoing imaging procedures. The bottles (118, 120) may be fluidly connected to a cassette (114) that includes a saline valve (176) and a contrast valve (178) operable to control flow from the saline bottle (118) and the contrast bottle (120), respectively. The cassette (114) may be fluidly interconnected to the multi-use tubing set (110) that is, in turn, fluidly connected to syringes (86a, 86b) on a powerhead (50) and a patient-specific tubing set (112). The patient-specific tubing set (112) may be replaced between patients and may also serve to isolate the remainder of the multi-dose injection system (108) from contamination from bodily fluids.

Abstract: The invention is an interface device and system for establishing an operating interface between an injector device and diagnostic imaging equipment. In one embodiment, the interface device may permit an operator to concurrently operate and control the injector device and the imaging equipment. The interface device may permit the injector system and the imaging system to communicate information regarding their current and future operational status with each other. The interface device may be used to synchronize the operation of the imaging equipment and the injector device. In one embodiment, the injector device and the imaging equipment may be able to communicate with each other directly or through the interface device via a communications protocol comprising binary logic signals. The binary logic signals may comprise one or more of a low strength signal, a high strength signal, an oscillating signal that oscillates between low and high signal strength, and combinations thereof.

Abstract: A system for at least partially filling and marking a cavity at a site within a patient's body includes a marker delivery device having a chamber configured to contain a marking substance and having a mechanism configured to expel the marking substance. A quantity of the marking substance is contained within the chamber of the marker delivery device. The marking substance is configured to at least partially fill the cavity and form therein a porous bioabsorbable body. A delivery tube is coupled in fluid communication with the chamber of the marker delivery device. The delivery tube has a distal end with a discharge port through which the marking substance is expelled. A releasable remotely detectable distal tip is coupled to the distal end of the delivery tube and is configured to be released to remain within the porous bioabsorbable body within the cavity upon the formation thereof.

Abstract: A pressure sensor suitable for use in a powered contrast injector system may be tested to help validate the operability and/or integrity of the sensor. In some examples, the pressure sensor may be tested by generating a pressure pulse in a fluid line fluidly connected to the pressure sensor so as to generate a first pressure reading. A high pressure fluid at a pressure above a maximum operating pressure of the pressure sensor may be conveyed through a valve fluidly connected to the pressure sensor. Subsequent to conveying the high pressure fluid through the valve, the pressure sensor may again be tested by generating a pressure pulse in the fluid line fluidly connected to the pressure sensor so as to generate a second pressure reading. In some examples, the first pressure reading is compared to the second pressure reading to determine whether the pressure sensor has passed or failed.

Abstract: The preset invention provides a liquid injector in which, when an injection time period and an injection rate are entered as an injection condition, a condition image having a horizontal width corresponding to the injection time period and including the injection rate as text data is displayed in a condition screen with its vertical axis representing the injection rate and its horizontal axis representing the injection time period at a vertical position in association with the injection rate and a horizontal position in association with the injection time period. The operator easily understands instinctively the injection condition from the horizontal width and the position of the condition image, and since the condition image includes the injection rate as text data, the operator can check quickly the numerical values. Thus, the liquid injector can be provided which allows simple entry and review of the injection condition.

Abstract: To provide a leak detecting sensor capable of favorably detecting a leak of a chemical liquid regardless of orientation in fixing to a patient. The leak detecting sensor has a plurality of light-emitting elements 11 each emitting light to be applied to the patient, and a single light-receiving element receiving the light emitted by the plurality of light-emitting elements and reflected by the patient. The plurality of light-emitting elements are placed to surround the single light-receiving element.

Abstract: Systems and methods are presented for the visual indication of whether a power injector has discharged fluid from a power injector syringe in a previous medical procedure. In this regard, the systems and methods generally provide for a power injector and a syringe for use with the power injector. The syringe includes a visual indicator (164) that moves between a first state and a second state at approximately the same time that the power injector discharges fluid from the syringe such that an operator may view the change in state.

Abstract: A locking syringe with an integrated bias member, for delivering medical fluids at high pressure, can include a housing, a shaft, a piston, a cap assembly, a bias member, and a locking member. A distal end of the housing can interface with a patient delivery apparatus. A piston can be connected to the distal end of the shaft and can include a peripheral sealing surface that can slidably engage the inside surface of the housing to form a movable seal. The cap assembly at the proximal end of the housing can engage the shaft. A base cap can secure the piston within the housing. The bias member can have a distal end coupled to the piston and a proximal end restrained, such as to help pressurize the internal cavity. The user-actuatable locking member can user-selectively engage and inhibit unwanted movement of the shaft.

Abstract: The inside of a cylindrical body is divided into two parts, that is, a first and a second chamber, and in a piston body, a first ventilation hole and a first ventilation path of a pushing portion are formed so as to communicate with the first chamber and a second ventilation hole and a second ventilation path of the pushing portion are formed to communicate with the second chamber, and a spring for returning the piston body to its original position is provided. By pressing the pushing portion while closing the first ventilation port so as to advance the piston body, air is supplied through a syringe port on the first chamber, while by pressing the pushing portion while closing the second ventilation port, air is supplied through the syringe port on the second chamber, and by releasing the pushing operation, the piston body automatically returns to the original position.

Abstract: One embodiment provides a method of using contextual lighting to assist a user of a medical fluid injection system. In this embodiment, the method includes providing a lighted display in proximity to a component of the injection system during setup of the medical fluid injection system. If the user has properly performed a setup function that is associated with the component of the injection system, the method further comprises providing a first visual indication on the lighted display. If the user has not properly performed the setup function that is associated with the component of the injection system, the method further comprises providing a second visual indication on the lighted display.

Abstract: An angiographic injector system and a method of controllably delivering medical fluid to a patient from an angiographic injector system are disclosed. A multiple processor control system is used to actively control the injection process and to monitor sensed functions of the system. The multiple processors provide dual redundancy safety circuits for critical control functions such as syringe motor drive speed and current. A motor/servo-amplifier nested control function is also disclosed. A unique method and apparatus are disclosed for establishing injection parameter default values just prior to an injection procedure that are based on physiological values of the patient to be treated. The injector system uses an interactive display panel that presents sequenced set-up screens to the user and which enables the user to select injection procedures, parameters and other modes of operation directly through the interactive panel.

Abstract: Various embodiments of syringe plunger driver or ram retraction protocols for a power injector are disclosed. In a first ram retraction protocol (184a), a first ram may be partially retracted (232), followed by a full retraction of a second ram (234), followed by a completion of the retraction of the first ram (238). In a second ram retraction protocol (184b), a first ram may be partially retracted (252), followed by a partial retraction of a second ram (254), and sometime thereafter each of the first and second rams may be completely retracted (260, 262). In a third ram retraction protocol (184c), the first and second rams are simultaneously and partially retracted (272), and sometime thereafter each of the first and second rams are completely retracted (276). In a fourth ram retraction protocol (184d), the first and second rams are simultaneously and fully retracted (292) based upon a programmed input or the like.

Abstract: A device for administering a liquid preparation comprising a pharmaceutical agent, particularly a contrast agent, in the form of a bolus. The device comprises in particular a core cylinder and an external cylinder, the core cylinder comprising a conduit (107) and a cylindrical reservoir (108) cooperating with a respective plunger (109), wherein the plunger is modified in order to operatively engage with guiding means (300) provided on the external cylinder.

Abstract: One embodiment provides a method of using contextual lighting to assist a user of a medical fluid injection system. In this embodiment, the method includes providing a lighted display in proximity to a component of the injection system during setup of the medical fluid injection system. If the user has properly performed a setup function that is associated with the component of the injection system, the method further comprises providing a first visual indication on the lighted display. If the user has not properly performed the setup function that is associated with the component of the injection system, the method further comprises providing a second visual indication on the lighted display.

Abstract: A marker deployment tool may comprise a marker cannula having a lateral deployment aperture, a push rod slidably disposed within the marker cannula and a scalloped tip coupled to the distal end of the marker cannula. The scalloped tip may have a push rod recess configured to receive a portion of the distal end of the push rod such that the push rod does not appreciably extend out of the lateral deployment aperture when the push rod is actuated distally. The marker deployment tool may further comprise a magnet at or near the distal end. This magnet may be used in combination with a magnet or plurality of magnets disposed about an access chamber in a tissue sample holder to assist the user in aligning the marker deployment tool. The access chamber in the tissue sample holder may also include a valve, two valves, or a removable plug.

Abstract: A method is disclosed in which a vapor-deposited coating or layer is directly or indirectly applied to at least a portion of the internal wall of the barrel of a capped pre-assembly comprising a barrel, optionally a dispensing portion, and a cap. The cap is secured to the barrel and at least substantially isolates the distal opening of the dispensing portion from pressure conditions outside the cap. A vapor-deposited coating or layer is applied directly or indirectly to at least a portion of the internal wall of the barrel while the pre-assembly is capped. The coating or layer is applied under conditions effective to maintain communication from the barrel lumen to the exterior via the front opening, optionally further via the dispensing portion lumen if present, at the end of the applying step. The capped pre-assembly can be pressure tested easily and rapidly, for example with a test duration between 1 and 60 seconds, to determine whether it has container closure integrity.

Abstract: Chemical liquid injector 100 includes two piston driving mechanisms 130 each moving a piston of a syringe forward, main injection condition determining section 171 determining injection conditions for a chemical liquid in main injection, test injection condition determining section 172 determining injection conditions for the chemical liquid in test injection performed prior to the main injection to inject a smaller injection amount of the chemical liquid than that in the main injection, and control section 161 creating an injection protocol in accordance with the injection conditions determined by test injection condition determining section 171 and main injection condition determining section 172 such that the chemical liquid is injected in a series of operations in which the test injection is performed, then a preset injection suspension time is present, and subsequently the main injection is performed, and further controlling operation of piston driving mechanisms 130 in accordance with the injection prot

Abstract: A system for safely delivering gas through a medical device to a patient and a method for using an exemplary system are disclosed. The system may be configured to minimize the risk of delivering an unwanted gas through mix up or mistake. A pneumatic fitting for use in medical procedures is also disclosed. The fitting may be configured to mate exclusively with a specific gas or fluid source.

Abstract: To provide a mixing device, a mixing tube, a drug solution injecting system, and a drug solution mixing method capable of evenly and efficiently mixing a plurality of kinds of drug solutions. The mixing device according to the present invention includes: a swirling flow generating chamber; a first inflow opening for introducing a first drug solution into the swirling flow generating chamber in a direction parallel to a central axis of the swirling flow; a second inflow opening for introducing a second drug solution into the swirling flow generating chamber so as to generate a swirling flow of the second drug solution having a specific gravity lower than that of the first drug solution; an outflow opening for discharging a mixed drug solution; and a narrowing chamber which is interposed between the swirling flow generating chamber and the outflow opening and has a space continuously narrowed toward the outflow opening.

Abstract: A drive ram for use with a medical fluid injector may include a central, longitudinal reference axis. First and second gripper members may be pivotally interconnected with a plunger engaging end of the drive ram. Each of the first and second gripper members may be pivotable about a common pivot axis that intersects the reference axis. Each of the gripper members may further include a first end that is remote from the common pivot axis. In some embodiments, the first and second gripper members may be pivotable between a first position and a second position. In the first position, the first ends of the gripper members may be spaced apart by a first distance, while in the second position, they may be spaced apart by a second distance that is greater than the first distance.

Abstract: A medical fluid injector device injecting a patient with a mixed medical fluid provided by a plurality of medical fluids and capable of simply setting injection conditions for the mixed medical fluid. A medical fluid injector (100) includes an injector head (110) injecting a diluted contrast medium into a patient and a controller unit (50). The controller unit (50) performs a process of receiving an input relating to an injection rate of the diluted medical fluid, a process of receiving an input relating to a mixture ratio by an operator, a process of calculating an injection rate of a contrast medium based on the mixture ratio, and a process of calculating an injection rate of physiological saline based on the mixture ratio. The injector head (110) injects the contrast medium and the physiological saline at the calculated injection rate of the contrast medium and the calculated injection rate of the physiological saline, respectively.

Abstract: A syringe product comprises a syringe barrel having a fluid-containment wall made using a polymer composition comprising a metallocene polypropylene polymer and an oganophosphate clarifier. The syringe product may be prefilled with an injectable medical formulation prior to use. The syringe product may be used to administer an injectable medical formulation to a patient.

Abstract: Device for administering heat to a cavity, tissue or vessel, characterised in that it takes the form of an insulated copper wire over the length of which is crimped a tube having a resistivity of more than 20 ??·cm, the copper wire (1) is in contact with the said tube at its distal extremity, the tube is enclosed over part of its length by at least one movable cylinder having an electrical resistance of less than 20 ??·cm, and the movable cylinder and the copper wire have means for connection to a current generator.

Abstract: A medical fluid injector, replaceable syringe, and coupling mechanism to engage the syringe plunger to the plunger drive ram of the injector are provided wherein coupling involves a cam cleat-like mechanism, thereby allowing for cooperative movement between the plunger drive ram and syringe plunger. The coupling mechanism of the plunger drive ram is provided with first and second movable members, each having toothed, arcuate surfaces, while the coupling mechanism of the syringe plunger is provided with a knurled cavity. Disengagement of the coupling mechanism is facilitated by translational movement of a face plate located on the forward end of the injector housing.

Abstract: An endoscope apparatus includes a light source device, an endoscope, a processor, and an observation monitor. The light source device switches between excitation light EX that excites a connective tissue in a submucosa of a tissue within a body cavity, narrow-band light NBa absorbed by a blood vessel running through the submucosa or muscularis propria, and narrow-band light NBb absorbed by a substance locally injected into the submucosa, and radiates the selected light. The processor generates a plurality of image signals, images of which are picked up by a CCD of the endoscope and the observation monitor synthesizes a plurality of images and displays the synthesized image.

Abstract: Embodiments include a fiducial deployment system including a needle and at least one splayed-end fiducial retained within the needle by frictional engagement and/or by engagement of the splayed end with one or more distal detents in the needle's lumen. A fiducial may include one or more splayed portions configured to engage the wall of the needle lumen, which may include one or more detents. The needle, which may include echogenic enhancements, may be configured to deliver a plurality of fiducials to a target location in serial fashion, one at a time. A variety of splayed-portion fiducials are disclosed.

Abstract: The present disclosure relates to an injector containing a processor, a pump or a motor with advance for a piston, which is suitable for driving liquid out of a cartridge, a data storage device, a device for data transfer, wherein the processor is electronically connected to the data storage device, to a control unit for the pump or the motor, and to the device for data transfer; wherein the injector is suitable for being connected to a container or a cartridge for fluid transfer, which container or cartridge contains a multiplicity of doses of a parenteral solution; wherein a data storage device is fixedly connected to the container or the cartridge; wherein the device for data transfer is suitable for reading out information from the data storage device on the container or the cartridge; and wherein at least one specification in respect of the identity of the product stored in the container or in the cartridge is stored in the data storage device on the container or the cartridge.

Abstract: Medical apparatus and processes controllably generate medically useful micro or nano bubbles of medically desirable and controllably selectable size, size distribution, homogeneity and concentration (and/or other key bubble parameters) for patient infusion, and/or which may incorporate therapeutic or other agents for patient infusion and/or may be combined with therapeutic or other agents prior to infusion into patients. The bubble generation apparatus and processes controllably permit the adjustment and selection of key bubble parameters through bubble generation actuation and orientation techniques and through selection of bubble fluid compositions in order to facilitate medical research and/or to optimize treatment for imaging, therapy, sonoporation, inertial and non-inertial cavitation, and acoustic activation, among other medical uses. Disposable cartridges containing such bubbles are provided and may include means for patient infusion.

Abstract: A system to minimize fluid turbulence inside a tissue cavity during endoscopic procedures. A body tissue cavity of a subject is distended by continuous flow irrigation using a solenoid operated pump on the inflow side and a positive displacement pump, such as a peristaltic pump, on the outflow side, such that the amplitude of the pressure pulsations created by the outflow positive displacement pump inside the said tissue cavity is substantially dampened to almost negligible levels. The present invention also provides a method for accurately determining the rate of fluid loss into the subject's body system during any endoscopic procedure without utilizing any deficit weight or fluid volume calculation, the same being accomplished by using two fluid flow rate sensors. The present invention also provides a system of creating and maintaining any desired pressure in a body tissue cavity for any desired cavity outflow rate.

Abstract: A contrast media injection system includes detects the absolute position of the syringe ram using a non-contact sensor. A series of magnets and Hall-Effect sensors may be used or an opto-reflective system. Illuminated knobs that are connected to the drive mechanism for the syringe ram rotate with the drive and provide visual feedback on operation through the illumination. Analog Hall-Effect sensors are used to determine the presence or absence of magnets that identify the type of faceplate being used. The faceplates include control electronics, connected to the powerhead through connectors, which may be interchangeably used by the two faceplates. The faceplate electronics include detectors for automatically detecting the capacity of pre-filled syringes.

Abstract: A power assisted method and injector device for controllably delivering to patients a dispersion medicament or diagnostically active agent, the homogeneity of which is preserved throughout delivery. Diagnostically active agents disclosed are gas microbubble suspensions useful in ultrasonic diagnostic imaging and liposomal formulations in which liposome vesicles are loaded with iodinated compounds.

Abstract: A medical apparatus includes: a first vessel for supplying a first liquid; a second vessel for supplying a second liquid; a mixing vessel for mixing the first and second liquids; a connector including a first flow passage connected to the first vessel, a second flow passage connected to the second vessel, a third flow passage connected to the mixing vessel and joined to the first flow passage and the second flow passage, and a discharge port which communicates with the third flow passage; and a flow passage opening/closing device provided in the third flow passage at a joint part where the first flow passage and the second flow passage join the third flow passage or at a part on a discharge port side relative to the joint part and which is operative to open/close the third flow passage.

Abstract: To facilitate imaging of a patient two different image recording methods are to be carried out at the same time. An auxiliary fluid, for example a contrast medium or a tracer, may be introduced into the body in each image recording method. The invention proposes mixing the two auxiliary fluids in situ immediately before dispensing to the patient. For this purpose it provides an injector with which the auxiliary fluids may be mixed and supplied to the patient. Devices for controlling dispensing of fluid from containers connected to the injector to produce a mixed solution may be electronically controlled by a control unit which calculates the total quantities, and optionally sub-quantities, of auxiliary fluids, which are used for a mixed solution, before activating the devices.

Abstract: An injector for injecting fluid from at least one syringe. The syringe having a plunger. The injector includes a drive member operable to engage the plunger of the syringe. A control system configured to control the at least one drive member. At least one mode operable from the control system. The mode of operation selected from the group consisting of at least one of a sequential injection mode or a simultaneous injection mode.

Abstract: A bladder syringe for a fluid delivery system includes a cylindrical body, a cap-bladder assembly, a plunger element disposed in the cylindrical body, and a mounting assembly to secure the cap-bladder assembly to the cylindrical body. The cylindrical body has a distal end and a proximal end and defines a throughbore. The cap-bladder assembly is adapted for connection to the distal end of the cylindrical body, and includes a cap body and a bladder. The cap body defines an interior cavity and a distal discharge conduit and is adapted to engage the distal end of the cylindrical body. A disc-shaped bladder is disposed within the interior cavity and typically includes a central membrane portion. The plunger element is disposed in the throughbore of the cylindrical body and is vented to enable evacuation of the space between the plunger element and the cap-bladder assembly in the cylindrical body.

Abstract: A system consisting of a hand-piece with a lever operated hydraulic pump and a fluid reservoir, a connecting tube and a remote connector which will seal to a syringe body which contains a viscous material. The pump expels fluid from the reservoir into the top of the syringe via the connecting tube where the fluid presses on the syringe plunger expelling the viscous material from the primary chamber of the syringe.

Abstract: Embodiments of the present invention describe methods of determining the occlusion of body lumens and apparatuses for doing so. In one particular embodiment, the occlusion of the fallopian tubes by an intrafallopian contraceptive device may be confirmed by contrast enhanced ultrasonography (also known as stimulated acoustic emission hysterosalpingo-contrast sonography). In these embodiments a contrast agent containing microbubbles is used.

Abstract: A chemical liquid injector comprises liquid syringe 200 and a chemical liquid injector. Liquid syringe 200 has cylinder member 210, a piston member and RFID tag 230 put on an outer circumference of cylinder member 210. The chemical liquid injector has cylinder holding mechanism 120 for holding cylinder member 210, a piston driving mechanism for driving the piston member and an RFID reader. The RFID reader has reader antennas 132L, 132R placed opposite to a tag antenna so as to be able to receive data from RFID tag 230 with cylinder member 210 is appropriately held by the cylinder holding mechanism. The piston driving mechanism is permitted to operate only when the RFID reader receives data from RFID tag 230.

Abstract: A method of securing a biopsy marker within a biopsy site includes depositing a marker element within a biopsy site and fixing the marker element within the biopsy site by injecting a securing agent within the biopsy site. Delivery devices for delivering the securing agent to the biopsy site are also disclosed.

Abstract: A method to perform high resolution tissue ablation including the steps of forming a beam to deliver optical energy and providing an energy dissipating material is provided. The steps of selecting an area of interest in a target tissue and placing the energy dissipating material adjacent to the area of interest may be included. The steps of directing the beam to the area of interest and scanning the beam across the area of interest to ablate the target tissue may be further included. Also provided is an apparatus and a system for high resolution tissue ablation including a beam to provide optical energy and an injector for placing an energy dissipating material adjacent to an area of interest. Further, the apparatus and system may include at least a mirror and a lens for directing the beam to the area of interest and scanning the beam to ablate target tissue.

Abstract: A hand-held remote for a medical fluid injector includes a syringe and a conduit which may be coupled to a pressure transducer on a control circuit of the injector. Movement of a plunger within a syringe body on the syringe creates a pressure which is sensed by the pressure transducer and the control circuit responds to the sensed pressure by causing fluid to be ejected from, or drawn into, a syringe mounted to the injector. The pressure developed by the remote provides tactile feedback to an operator for improved control over injections.

Abstract: A power injector syringe assembly (170) is disclosed. The assembly (170) includes a coupling (130?) and a syringe cradle (180) that extends from the coupling (130?). The coupling (130?) and cradle (180) may be integrally formed. In any case, the coupling (130) includes a wedge-shaped mounting flange (144) to facilitate installation of the assembly (110) on a syringe mount (200) of a power injector. The coupling (130) also includes at least one coupling member (150) to facilitate removal of the assembly (110) from the syringe mount (200). At least one part (186) of the cradle (180) extends no more than 180° about a long axis (176) of the cradle (180), while a syringe retention section (188) of the cradle (180) does extend more than 180° about this long axis (176).

Abstract: An improved system for mammography analysis and methods of using the same. In one aspect, the present invention provides a biopsy instrument having a side opening that generally coexists or is aligned with a central portion of a cyst, tissue or otherwise for deploying a marking device to the central region of the same. In another aspect, the present invention provides an encasement, adapted to receive a marking clip, for deployment into a tissue region for marking and/or treatment of the same.

Abstract: A syringe for injecting contrast injection media into a patient. An inlet valve system associated with the syringe, the inlet valve system operable with a contrast injection media having any viscosity within the range of about 1 cP to about 30 cP. An inlet valve system associated with the syringe, the inlet valve system including a valve member having a density of less than or equal to 1 gram per cubic centimeter. A contrast injector system with such a syringe.