Abstract: The present invention provides a closed loop fat transplantation system newly designed to aspirate a fat, to handle it without receptacle transfer and to transplant it into the human body, which is composed of a fat transplantation receptacle (hereinafter referred as FT receptacle) and an exterior mechanical pressurization and decompression means. The said FT receptacle includes a vertical hem portion where joining selectively individual syringe needle or cannelae, a cylinder-shaped receptacle into front fat storing space and rear pressurization and decompression space. The said pressurization and decompression means can give positive/negative pressure to the fat storing space through the piston head of the said FT receptacle and it has a structure separable from the said FT receptacle. Accordingly, fat transplantation can be performed without receptacle transfer using the same FT receptacle extracting fat from patient's body giving negative pressure through the piston head to the fat storing space.

Abstract: In one embodiment a large volume syringe pump assembly with a mechanism for facilitated manual driving (100) is connected to a large bore access cannula (200) which is placed percutaneously into the arrested left ventricular cavity of a victim. The cannula is equipped with balloons for sealing (212) and for immobilization (218). A large bore 3 way stopcock (208) is incorporated into the proximal end of cannula. The syringe pump assembly includes a large volume syringe (140) with a vent for air removal (141). A tubing length (148) is incorporated into the distal end of syringe. Tubing length has a connector at its distal end (150) for rapid connection to cannula. The syringe pump assembly includes a lever (122) pivotal attached to the syringe. By rearward manual movement of the lever the oxygenated blood is aspirated from the left ventricle and from the left atrium into the large volume syringe.

Abstract: The present invention pertains to a miniature flexible thrombectomy catheter having one or more flexible miniature noncollapsing tubular portions including pushable and torqueable structure for introduction into the smaller vessels in neurovascular regions. A jet body having an arcuate fluid jet emanator is incorporated in order to minimize size at the distal portion of a minimally sized catheter tube.

Abstract: A portable system for subatmospheric pressure therapy in connection with healing a surgical wound is provided. The system includes a wound dressing dimensioned for positioning relative to a wound bed of a subject, and a collection canister in fluid communication with the wound dressing. The canister includes a base defining a fluid receiving cavity and having a fluid inlet port and a vacuum port. The fluid inlet port is configured for fluid communication with a wound dressing. The system further includes a cover selectively engageable to the base, e.g., in a snap-fit manner. The cover is configured to receive a control unit and has a vent assembly for exhausting the control unit. A seal member is interposed relative to the base and the cover to establish and maintain a substantial sealed relationship between the two components when assembled.

Abstract: Device and method for rapid extraction of body tissue from an enclosed body cavity. Hollow entry cannula with optional core element provides entry into body tissue space such as bone marrow. Aspiration cannula is inserted through cannula into body tissue and is manipulated to advance directionally through body cavity. Optional stylet within aspiration cannula aids in advancing aspiration cannula through body tissue and is removed to facilitate extraction of body tissue through the aspiration cannula. Inlet openings near distal tip of aspiration cannula allow tissue aspiration, with negative pressure source at proximal end of aspiration cannula providing controlled negative pressure. Aspiration cannula may be withdrawn and its path adjusted for multiple entries through the same entry point, following different paths through tissue space for subsequent aspiration of more tissue.

Abstract: Embodiments of the invention provide a suction evacuation system, or smoke evacuation system, for incorporation into hand-held surgical devices. In particular, the system according to embodiments of the invention can be used in hand-held surgical suction-irrigation devices that may also include electrical systems which deliver energy to effect cutting, ablation and coagulation effects at the surgical site. Embodiments of the invention provide a smoke evacuation system that can be incorporated into a hand-held surgical device wherein the smoke evacuation system is structurally and functionally integrated with the suction control system of the device.

Abstract: A pumping system for use in medical applications where liquids must be infused and aspirated from a mammalian patient, and whose economics are such that it is cost effective to simply dispose of it after a single use. The system features positive displacement pump(s) such as reciprocating pump(s) containing a damping mechanism to dampen out the peaks and valleys in the fluid pressure that is pumped, which is important for preventing cavitation. The system furthermore features a shut-off valve on the extraction side so that certain injected fluids such as contrast medium, are not immediately pumped out of the patient. In a preferred embodiment, the system also features means for independently controlling the fluid pressure/volume on the infusion and extraction sides, self-priming capability, a continuous fluid path, and visual air bubble detection, with viewports located at important points in the fluid path, such as at pumps and valves.

Abstract: The devices and methods shown provide for the minimization of extravasation during arthroscopic surgery. The extravasation minimization device allows a surgeon to drain excess fluids from the soft tissue surrounding the surgical field while also providing a stable surgical portal for arthroscopic surgical instruments.

Abstract: A surgical system with irrigation and aspiration lines having different compliance or stiffness, with the irrigation line having a higher compliance than the aspiration line.

Abstract: An irrigation/aspiration tip having a relatively rigid cannula attached to a hub and an open end opposite the hub. Coaxially and removable received over the tip is a soft elastomeric or rubber sleeve. The sleeve forms a gap between the sleeve and the cannula, the gap allowing irrigation flow. The distal end of the sleeve is closed by a cap of reduced diameter. The reduced diameter of the cap seals the distal end of the cannula. The relatively soft cap reduces the likelihood that the posterior capsule will tear during cortical clean-up and capsule polishing. Removing the sleeve allows the cannula to be resterilized an unlimited number of times, thereby allowing unlimited reuse of the cannula.

Abstract: Methods and systems are provided for a sub-atmospheric wound-care (SAWS) system for treating an open wound. The SAWS system includes a regulated vacuum source for developing a negative pressure, a flow rate meter configured to measure a flow rate of liquid removed from the wound, a primary pressure regulating sensor located proximate the wound for directly measuring the negative pressure at the wound, a backup pressure regulating sensor located vacuum tube, a porous dressing suitable to be sealed airtight which is positioned within a wound interface chamber, a collection canister configured to collect said liquid removed from the wound, and an adapter configured to use wall suction a primary regulated vacuum source.

Abstract: Steering engagement catheter devices, systems, and methods of using the same for accessing tissue, including the internal and external tissues of the heart, are disclosed. In at least one embodiment, a steering engagement catheter is provided, comprising an elongated tube having a proximal end, a distal end, and a first wall positioned circumferentially along a length of the elongated tube, the elongated tube configured such that a delivery catheter is capable of at least partial insertion into the elongated tube, at least one steering wire having a proximal end and a distal end, the distal end of the steering wire coupled to the first wall of the elongated tube at or near the distal end of the elongated tube, and a controller operably coupled to the at least one steering wire at or near the proximal end of the at least one steering wire.

Abstract: A device suitable for removing material from a living being is provided, featuring an infusate pump, and an aspiration pump, both powered by a motor. The aspiration pump and infusate pump preferably feature a helical pumping mechanism, and operate at a high rate of rotation, thereby ensuring adequate pumping performance and flexibility. Additionally, a narrow crossing profile is maintained, ensuring that the device may reach more tortuous regions of the vasculature.

Abstract: A surgical system including a surgical glove having support systems such as, but not limited to, lights, electrical cautery, suction, and irrigation. The surgical glove may include one or more lights, electrical cautery, suction, and irrigation positioned on distal ends of fingers of the surgical glove. The support systems may be controlled with switches positioned on the fingers upon which each support system is positioned. The switches may be operable with the thumb on the human hand upon which the surgical glove is attached. The surgical system may also include a surgical gown having a connection system for attaching support conduit to the surgical gown. The surgical system enables a surgeon to have a plurality of support systems immediately available and reduces entanglement problems endemic with conventional systems.

Abstract: Wound fluid blood detection systems and methods are described that are operable in conjunction with reduced pressure wound treatment (RPWT) systems, as well as ancillary therapy and monitoring systems applied concurrently with RPWT systems. The blood detection monitor operates by optically characterizing the content of wound fluids to the extent of identifying percentage blood content. This identification relies upon the transmission of select wavelengths of light across a volume of wound fluid to a photo detector (connected to signal processing instrumentation) capable of quantifying the absorption characteristics of the fluid. The detection components may be implemented in conjunction with either a fluid flow conduit (i.e. the reduced pressure tubing directing fluid away from the wound dressing) or more directly in association with the materials that comprise the wound dressing positioned within the wound bed itself.

Abstract: A system and apparatus for irrigating a surgical site during an electrosurgical procedure are disclosed. The system includes a hand piece having an elongated housing connected to a multilumen tube extending proximally from the housing and having an irrigation tube for delivering irrigation fluid, a suction tube for withdrawing irrigation fluid, and electrical wiring, a first controls for adjusting flow of irrigation fluid within the irrigation tube and second controls for adjusting flow of irrigation fluid within the suction tube. A valve cassette is connected to the multilumen tube, which includes an irrigation valve configured to control the flow within the irrigation tube and a suction valve configured to control the flow within the suction tube. A hardware control module controls the irrigation valve and the suction valve based on control signals from the first and second controls.

Abstract: An interventional catheter assembly comprises an operating head for removing obstructive material from a target site in a body lumen or cavity and at least one aspiration port located proximal to the operating head and penetrating the catheter assembly, the aspiration port being in communication with a sealed lumen that communicates with a vacuum system for withdrawing aspirate fluid and obstructive material from the target site. The interventional catheter incorporates an elongated guidewire lumen bushing extending proximally from a distal region of the operating head to reduce the clearance between the guidewire and the internal surface of the guidewire lumen during operation of the interventional catheter. This feature restricts entry of fluid and debris into the guidewire lumen and promotes maintenance of consistent and high aspiration pressure and volume during operation of the aspiration system and interventional catheter assembly.

Abstract: In various embodiments, an ophthalmic surgical instrument may include an aspiration tube, an irrigation/aspiration tip (formed of a first material such as plastic), and a patch, coupled to the irrigation/aspiration tip, made of a second material (e.g., silicone) having a higher coefficient of friction than the first material. In some embodiments, the patch may be placed on the irrigation/aspiration tip in a position to allow a user of the irrigation/aspiration tip to manipulate an intraocular lens (IOL) through contact between the patch and the IOL. For example, the patch may be positioned on a side of the irrigation/aspiration tip opposite an aspiration port or on a distal end of the irrigation/aspiration tip. In some embodiments, the patch may be formed separately and coupled to the irrigation/aspiration tip through an adhesive or may be molded onto the irrigation/aspiration tip. In some embodiments, the patch may include features to increase friction.

Abstract: A suction catheter having an elongated flexible hollow member and a spoon-shaped distal end designated to assist manual removal of large airway occluding particles from the oropharynx and mouth opening to near the epiglottis of a patient by an emergency caregiver. The tip of the spoon-shaped distal end defines an ovular orifice of sufficient size to remove both viscous and non-viscous matter including matter from the airway of the patient for conveyance through the hollow member. The catheter includes a flexible stylet member therein to permit bending of the catheter and causing it to retain its bent shape with the proximal end thereof away from the patient. An opening is provided in the catheter and communicates with internal airway for use in controlling the amount of suction provided by the connection of the proximal end of the catheter to a vacuum source.

Abstract: Interventional catheter assemblies, operating systems and adaptive interface components allow operation of a variety of interventional catheter assemblies, including infusion catheters, aspiration catheters and interventional catheters that provide both infusion and aspiration, using a common control console housing infusion and aspiration systems. Control instructions for operating the interventional catheter assembly and authentication protocols for verifying system matches and operating conditions maybe encoded in hardware, firmware or software, such as a memory or storage device, provided in the interventional catheter assembly or in a discrete adaptive interface component. Adaptive components such as tubing cassettes routing aspiration and/or infusion tubing in a predetermined configuration to mate with aspiration and infusion systems on a control console are also provided.

Abstract: A surgical system including a surgical glove having support systems such as, but not limited to, lights, electrical cautery, suction, and irrigation. The surgical glove may include one or more lights, electrical cautery, suction, and irrigation positioned on distal ends of fingers of the surgical glove. The support systems may be controlled with switches positioned on the fingers upon which each support system is positioned. The switches may be operable with the thumb on the human hand upon which the surgical glove is attached. The surgical system may also include a surgical gown having a connection system for attaching support conduit to the surgical gown. The surgical system enables a surgeon to have a plurality of support systems immediately available and reduces entanglement problems endemic with conventional systems.

Abstract: The present invention provides a body passage cleansing device suitable for being passed through an internal channel of an endoscope, comprising a distal plug having a proximal end and a distal end, wherein said plug comprises channels, apertures and/or nozzles which are capable of allowing the passage of a fluid therethrough from said proximal end to said distal end, wherein said plug is connected to the distal end of a wire or other actuating means; wherein at least an outer portion of said distal plug is capable of being elastically deformed such that the external diameter and/or outline thereof may be reduced in response to inwardly-directed compression forces exerted thereon; and wherein said channels, apertures and/or nozzles are in a closed conformation when said distal plug is subject to said compression forces, and in an open conformation when said plug is not subject to said compression forces.

Abstract: The present invention relates to a device for providing spongy bone with bone substitute and/or bone reinforcing material, wherein at least one perforating device (4) is provided for making at least one hole (5) in the spongy bone (1) and wherein at least one flushing or rinsing device (6) is provided for flushing or rinsing the hole (5) with a rinsing agent (7). At least one vacuum source (9) is provided for generating a vacuum in the hole (5) in the spongy bone (1) for sucking and/or facilitating insertion or feeding of the bone substitute and/or bone reinforcing material (3) into said spongy bone (1). The invention also relates to bone substitute and/or bone reinforcing material and methods in connection with the invention.

Abstract: The present invention relates to a device for providing spongy bone with bone substitute and/or bone reinforcing material, wherein at least one perforating device (4) is provided for making at least one hole (5) in the spongy bone (1) and wherein at least one flushing or rinsing device (6) is provided for flushing or rinsing the hole (5) with a rinsing agent (7). At least one vacuum source (9) is provided for generating a vacuum in the hole (5) in the spongy bone (1) for sucking and/or facilitating insertion or feeding of the bone substitute and/or bone reinforcing material (3) into said spongy bone (1). The invention also relates to bone substitute and/or bone reinforcing material and methods in connection with the invention.

Abstract: An apparatus having a tube section and an expanded end. The tube section is flexible while the end section is rigid. The apparatus has a central bore, large enough to loosely receive an endoscope tube, and the end section has two peripheral bores which communicate with the central bore. There is a collar around the central bore which allows formation an air- and water-tight seal with the head of an endoscope. The tube may be fenestrated at its proximal end and may include medial pleats. This apparatus is mainly used by: sliding an endoscope into the central bore until the endoscope head forms an air- and water-tight seal with the central bore; connecting a lavage tube to one peripheral bore and a vacuum tube to the other peripheral bore; inserting the endoscope and the apparatus into a GI tract; and manually controlling the apparatus to apply lavage and vacuum.

Abstract: An aspiration instrument includes a compliant protective guard for minimizing injury to internal organs and other soft tissue while removing fluids from the body cavity. The compliant protective guard may be constructed from foam, plastic or other like material, including polyethylene and polypropylene. A preferred embodiment of the protective guard takes the shape of a bell. The compliant guard may be connected with the aspiration instrument using adhesives, such as glue or epoxy, or with a snap or friction fit. The compliant guard may define a single opening in fluid communication with the yankauer. The compliant guard may also define a plurality of openings for removing fluids from the body.

Abstract: A vacuum pump capable of pumping solid, liquid and gas, or any combination thereof, including a drive (40) and a manually disengageable pumping system connected thereto. The pumping system is composed of a two- or three-chambered canister (1, 18, 21) within which solids, liquids, and gases can be separated from one another. A highly flexible diaphragm (24) attached to the canister and sealed against it circumferentially, facilitates this separation, when reciprocating and pumping. The components of the pumping system are designed to be disposable, and the two- or three-chambered canister provides for a highly efficient pumping system that is significantly smaller in size than those previously known. The pump is particularly useful for medical applications.

Abstract: An apparatus and method to suppress vacuum surges in a surgical aspiration system is disclosed and claimed. A vacuum surge suppressor includes a first fluid path for coupling to a surgical instrument, and a filter attached to the first fluid path. A flow restrictor is coupled to the filter with the filter disposed upstream of the flow restrictor. The vacuum surge suppressor also includes a second fluid path for coupling to a vacuum pump. The second fluid path is connected to the flow restrictor and disposed downstream of the flow restrictor. The second fluid path defines a path internal pressure. A third fluid path is coupled to the filter and is connected to the second fluid path, bypassing the flow restrictor. A valve in the third fluid path obstructs flow in the third fluid path in response to the path internal pressure.

Abstract: An interventional catheter assembly comprising a catheter for insertion and guidance to a target site in a body lumen or a cavity and an operating head mounted in proximity to a distal end of the catheter and comprising a system for removing obstructive material from the target site is provided. In certain embodiments, the catheter assembly includes at least one aspiration port located proximal to the operating head that communicates with a first sealed lumen for withdrawing fluids and obstructive material from the target site, together with at least one liquid infusion port penetrating the catheter and located proximal to the at least one aspiration port that communicates with a second sealed lumen for supplying fluid to a location in proximity to the target site.

Abstract: Apparatus and methods in which very small volumes of biological fluid-borne material, particularly large molecules such as proteins, may be selectively extracted from or delivered to interstitial fluid (in vivo or in vitro) by means of intra-parenchymal micro-probes inserted in the brain. The primary use of the micro-probe is in neuroscience research, clinical diagnostics or treatment of epilepsy and other neurological conditions; it may also be applied to other organs and biological systems. Eventual human clinical applications may include neurosurgical monitoring, functional tracking of devices or materials introduced in a surgical procedure, or cerebro-spinal fluid sampling.

Abstract: A dialysis machine valve manifold assembly includes a plurality of pneumatic valves; a plate including a first side and a second side, the plurality of pneumatic valves mounted to the first side of the plate, the second side of the plate defining a plurality of pneumatic flow paths; and a port header mounted removably to the plate, the port header including a plurality of ports configured to connect sealingly to pneumatic tubing, the ports in fluid communication with the pneumatic valves via the pneumatic flow paths defined in the plate.

Abstract: A portable device for cleaning a nasal passage is disclosed that includes: a first receptacle having a first opening and a first stop, a second receptacle, a power driven motor operable to deliver an adjustably continuous flushing pressure to the first receptacle and to provide an adjustably continuous vacuuming pressure to second receptacle. The portable device also includes a first pressure adjusting means operable to control the amount of the flushing pressure, and a second pressure adjusting means, operable to control the amount of the vacuuming pressure.

Abstract: A medical device and method of applying said medical device to deliver drugs and to remove thrombus or soft tissue clots from vascular or other lumens in a patient is presented. The medical device generally comprises an elongated tubular delivery member having a proximal portion and a distal portion that differ in rigidity and a leak-free connector that is in contact with the proximal portion of the delivery member and is compatible for use with fibrinolytic agents and application of a vacuum. The delivery member includes a metal core made out of multiple shaped-wire strands and a polymer overlay disposed about the core. The wire strands, which have both an A-side and a B-side, are helically wound to form a polygonal shaped lumen whose inner diameter is defined by the A-side of the strands.

Abstract: A colonic lavage catheter includes a head attached at an end of a suction tube and having both rearward and lateral fluid discharge openings. A pair of tubes extend along the suction tube with their ends attached to the head to place the rearward and lateral fluid discharge openings in fluid communication with a source of pressurized fluid. The suction tube includes a plurality of suction orifices through the outer wall along its length proximate the catheter head. A cleaning process may be performed by inserting the catheter head into the colon and then discharging fluid through the rearward openings to advance the catheter. At points along the colon, pressurized fluid may be discharged through the lateral discharge openings to lavage the adjacent walls of the colon, with suction being applied to draw the dislodged material into the suction tube through the suction orifices.

Abstract: The invention concerns a device (1) for irrigating and pressurizing a body cavity (2). Said device comprises a circuit consisting of at least one source (3), wherefrom flows a fluid under pressure, connected to a supply conduit (3) emerging in its downstream end into the cavity (2), a discharge conduit (20) for said fluid exiting from said cavity (2) and means for regulating (30) said fluid. Said regulating means (30) include first pumping means (31) capable of being temporarily engaged with the supply conduit (10), second pumping means (32) engaged with the discharge conduit (20). The two pumping means (31, 32) are operated at the same speed and in the same direction when they are engaged with their respective conduits (10, 20).

Abstract: Described herein are methods and devices for selectively applying fluids (particularly anesthetics) to a target tissue from within a blood vessel while minimizing the amount of fluid applied to non-target tissue. The injection catheters described herein may include an elongate body, a directional injector, and one or more holdfasts for securing the catheter before extending the injector. The methods of selectively applying anesthetic to a target structure generally include the steps of inserting an injection catheter into a body vessel, positioning the injection catheter within the body vessel near the target structure, anchoring the injection catheter before extending a directional injector from the injection catheter, and applying anesthetic from the injection catheter to the target structure.

Abstract: A system for collecting and disposing of liquid medical waste includes a fluid collection cart and a draining and cleaning station. The fluid collection cart includes a pair of containers, each of which includes a draining port and a cap. Each cap includes an outer portion having a flushing port and a bore formed therein and an inner portion having vacuum and patient ports formed therein. The inner cap portion is disposable and removably positioned within the bore of the outer cap portion. Liquid level detectors also communicate with each container. The cart also includes a regulator so a low vacuum level may be pulled on one of the containers while a full vacuum level is pulled on the other container. Fluids are collected in the containers via suction tubes connected to the patient ports. The flushing and drain ports of the containers are connected to corresponding flushing and drain connectors on the station when the containers are full so that they may be drained and flushed.

Abstract: An ultrasonic horn assembly is configured so that irrigating fluid can be supplied only to a vibrating tip portion of the ultrasonic horn and so that suction aspiration can occur through a portion of the ultrasonic horn not in contact with the irrigating fluid. Controllers supplying irrigation fluid during a surgical procedure and controlling suction aspiration via monitoring of fluid level in the patient cavity are operatively coupled one to another to coordinate control of the fluid level in the patient cavity. Circuitry controlling power, frequency and amplitude of the tip of the ultrasonic horn occurring as a result of operation of a source of ultrasonic signal generating power controls either or both the supply of irrigation fluid and the suction aspiration so as to minimize damping of vibration of the tip of the ultrasonic horn. An optical viewing element is provided to view the tip of the ultrasonic horn.

Abstract: A suction device which can protected before and after use. The suction device includes an elongated suction tube having a suction tip at one end. A retractable, protective sheath is connected to the tube and extends over the exposed length of the suction tube. A tip protector extends from the free end of the sheath, and includes an interference structure in the form of a plurality of spaced ribs protruding inwardly to engage and grip the suction tip. A hollow sheath housing is secured to the free end and a sheath inserter is secured to the suction tube proximate the connection end, with the sheath housing and the sheath inserter being shaped to insert the retractable sheath in the hollow sheath housing when the sheath is in a retracted position. The tip protector and the sheath housing can be portions of a unitary structure.

Abstract: To provide an irrigation/aspiration apparatus by which a trouble for an operator is reduced and handling is facilitated and which is capable of preventing a sharp decrease of pressure of an anterior chamber with a simple constitution. The apparatus has a chamber storing an irrigation liquid, a vent tube for making the liquid flow into an aspiration tube, a leading vent leading the liquid into the chamber from an irrigation tube, an outflow pipe extended in an up-and-down direction, an opening formed on a wall of the outflow pipe, of which a width is narrow and set such that an opening is closed by the liquid under surface tension when a liquid level of the liquid inside the chamber rises, an outflow vent to which the irrigation tube or a vent tube is connected, and an air chamber which is a space provided above an inflow hole of the outflow pipe.

Abstract: A method for administering a liquid medical substance in a vein. The method comprises inserting a plurality of tubular ducts into a target venous lumen, conducting a liquid medical substance via at least one of the plurality of tubular ducts (106, 215, 419, 602) for the administering thereof toward a venous wall (110, 410) at the target venous lumen in an ejection pressure, quantity and direction, and withdrawing a residue of the liquid medical substance from the target venous lumen, in a suction pressure, quantity and direction, for the conducting thereof via at least one different of the plurality of tubular ducts (130, 240, 400). A relation between the ejection pressure, quantity and direction and the suction pressure, quantity and direction limits the extent of the administering within the venous lumen to a predefined space.

Abstract: An infusion source provides for a fluid supply and an irrigation line interconnecting the fluid supply with an irrigation lumen of an ocular handpiece. An accumulator is disposed in fluid communication with irrigation line and the irrigation lumen includes an expandable wall for enabling accumulation of fluid within the tubular member during occlusion of the aspiration lumen, and enhanced flow of the fluid of the irrigation lumen upon clearing of the occlusion.

Abstract: The invention relates to a flow limiter (8) for a fluid flowing in an aspiration branch of a surgical system. which fluid is a surgical fluid and has emulsified particles in a surgical intervention, with a limiter element (81) that comprises at least one flow channel arrangement (9a) with at least one main channel (811) and at least one subsidiary channel (812) that opens into the main channel at an angle of greater than or equal to 90°. The invention also relates to a surgical system, in particular an ophthalmic microsurgical system for lens surgery.

Abstract: Provided is surgical instrument which can provide a field of view over surgical site by sucking blood from bleeding site during surgery on body tissue of patient and monitoring dark and deep surgical site, which operator cannot see with his or her naked eye, with small camera. The surgical instrument has substantially the same shape as a pair of scissors and includes first body, second body having shape symmetrical to that of the first body, hinge to which the first and second bodies cross and are rotatably coupled, and photographing unit provided in the hinge to photograph a surgical site between front ends of the first and second bodies. The photographing unit may include camera mounted in the hinge such that lens of the camera can be exposed through the center of the front surface of the hinge and configured to transmit photographed image data to monitor.

Abstract: The present invention provides a DC-AC frequency converter type mucus suction device having an electromagnetic pump, the pressure and the flow generated in which could be changed to satisfy the requirement of the mucus suction device. mucusThe mucus suction device of the present invention comprises an electromagnetic pump, a suction device and a frequency converter circuit, wherein the frequency converter circuit at least comprises an oscillator circuit, a bistable circuit, and a push-pull circuit, wherein the electromagnetic pump is supplied with AC obtained from the oscillation of DC in the frequency converter circuit, wherein the swing speed, frequency and amplitude of the swing arms vary with the oscillation frequency of the oscillator circuit, such that the suction pressure and the suction flow of the electromagnetic pump could further be changed to obtain the most appropriate pressure and flow of the mucus suction device.

Abstract: A drainage tube device for removing fluids by suction from a human or animal body comprises a coupling unit with first and second coupling parts that can be connected to each other in a leaktight manner, a first valve that is arranged in the first coupling part, and a drainage tube with an end that is directed towards the patient and is held in the second coupling part. The drainage tube has a multi-lumen design with a drainage conduit and at least one auxiliary conduit. This drainage conduit and at least one of said auxiliary conduits are in fluidic communication with each other at their end directed towards the patient and arranged inside the second coupling part. The drainage tube device further comprises a second valve, which is arranged in the second coupling part and which opens and closes the drainage conduit. The drainage tube device and the coupling unit according to the invention are of simple construction but nonetheless permit many functions.

Abstract: Methods and apparatuses for automatically switching different aspiration levels to an ocular probe are disclosed herein. The probe may be a phacoemulsification probe. A first aspiration level, supplied by a first pump, may be applied to the probe simultaneously with ultrasonic energy. A second aspiration level, supplied by a second pump, may be automatically switched from the first aspiration level. Control feed back of the pumps may be varied according to set thresholds.

Abstract: The invention relates to a surgical system (1) for controlling a fluid, said system having: an irrigation line (3), which is connected at one end to a first fluid container (2) for holding irrigation fluid (21), and which is connected at another end to a surgical handpiece (40), an aspiration inlet line (7), which is provided from the surgical handpiece (40) to an inlet (9) of a suction pump (8), such that fluid can be sucked through the handpiece (40) by the suction pump (8), a second fluid container (15) for holding the irrigation fluid (22), an aspiration ventilation line (14), which connects the second fluid container (15) to the aspiration inlet line (7), a venting valve (17), which is provided in the aspiration ventilation line (14) and can be switched as a function of a fluid pressure in the aspiration inlet line (7), wherein the second fluid container (15) can be filled via a filling line (18), wherein the filling line (18) is connected at one end (30) to the irrigation line (3), and wherein the fi

Abstract: Electrosurgical methods and apparatus for treating tissue at a target site of a patient. An electrosurgical instrument includes a shaft, having a shaft distal end and a shaft proximal end, and an electrode assembly disposed at the shaft distal end. The electrode assembly includes at least one active electrode disposed on an electrode support. The instrument is adapted for coupling to a high frequency power supply or electrosurgical generator. Each active electrode is adapted for removing tissue from a target site and/or for localized coagulation of the target tissue. In one embodiment, the instrument is adapted for laparoscopic procedures.

Abstract: A flow control device includes a housing having a motor chamber and a pump chamber. The motor chamber has an outlet for communication with a fluid collection device, and an inlet for communication with an aspiration line through which fluids are delivered into the motor chamber. First and second motor rotors are rotatably disposed in a flow path between the inlet and the outlet in the motor chamber, and a drive shaft is coupled to the first motor rotor. The pump chamber has an outlet for infusing fluid to a surgical site, and an inlet through which infusion fluids are delivered into the pump chamber. First and second pump rotors are rotatably disposed in a flow path between the inlet and the outlet in the pump chamber, where the first pump rotor is coupled to the drive shaft. The drive shaft drives the pump rotors at the same speed as the motor rotors, such that any surge in aspiration flow induces a similar surge in infusion flow.