Abstract: A personal care apparatus (1) is provided with a suction nozzle configuration (4) which has two different suction nozzles (15, 22) with two different suction sections (27, 26), wherein the suction nozzles (15, 22) are held adjustably in relation to each other along a path of motion (16) which is preferably perpendicularly to their suction sections (27, 26), so that by means of an adjustment of this type in each case one of the suction nozzles (15, 22) may be adjusted with its suction section (27, 26) into an operating position permitting suctorial interaction with an area of the skin.

Abstract: A method for packaging an agent for delivery within a body cavity. A reservoir within a package contains a specified quantity of the agent and is either contiguous with, or coupled to, a dispensing node such as a swab. Depth of insertion of the dispensing node into the body cavity is restricted to a specified depth by a penetration-restricting feature that forms part of the package.

Abstract: A protector effectively suppresses infections. The protector protects a tube entry part, where a tube passes through the skin of a living body, from infections, and includes a sticking part that is stuck onto the skin of the living body in a periphery of the tube entry part, and a covering that covers the tube entry part, forms an internal space that surrounds the tube entry part, and has a passage through which the tube passes. The covering is provided with an opening that can be freely opened and closed with a cap or the like.

Abstract: A disposable cushioned aspirator which forms part of a dental or medical aspirating system. The disposable cushioned aspirator appliance described herein is intended principally to be used in dental and medical procedures where body fluids and rinse water is evacuated from the site of a procedure. An elongate tubular element has a connection end and a patient end. The patient end is exteriorly lined with a layer of soft cushioning material such as a soft thermoplastic elastomers, styrene based polymers, rubber or a porous polymer foam material to define an aspirator tip that protects the soft tissues in and around the mouth of a patient. The soft aspirator tip has external longitudinal pressure relief channels and recessed aspiration openings within the channels for control of aspiration characteristics.

Abstract: A splash shield system for use in combination with various irrigation sources, particularly wide mouth irrigation squeeze bottles.

Abstract: Disclosed is a medical device used to prevent the cross-contamination of patients or injectors in which various components placed on the injector minimize or eliminate back splash contamination of the injector.

Abstract: A catheter having a tube and a tip connected to one end of the tube. The tip has a collar, an end member and lowered side walls positioned between the collar and the end member. The lowered side walls define an opening that is biased toward the end member.

Abstract: The present invention provides a coupling device for attaching a sleeve (40) to a surgical aspirator tip (10) that allows airflow between the external environment and the interior of the sleeve (40). The coupling device includes a male member (26) attached to the tip (10) and a female member (42) formed in the proximal end of the sleeve (40). The male member (26) includes at least one longitudinal groove (100). When the male member (26) is received into the female member (42), at least one venting channel (80) is defined between at least one longitudinal groove of the male member (26) and the inner surface of the female member (42). Venting channel (80) permits airflow between the external environment and the interior of the sleeve (40).

Abstract: A tissue closure treatment system and method are provided with an external patient interface. A first fluid transfer component FTC.1 comprises a strip of porous material, such as rayon, with liquid wicking properties. FTC.1 can be placed directly on a suture line for transferring fluid exuded therethrough. An underdrape is placed over FTC.1 and includes a slot exposing a portion of same. FTC.2 comprises a suitable hydrophobic foam material, such as polyurethane ether, and is placed over the underdrape slot in communication with FTC.1. Negative pressure is applied to FTC.2 through a connecting fluid transfer component FTC.3. A negative pressure source can comprises a manual device or a power-operated suction device. The tissue closure method includes a manual operating mode using a manual suction device with an automatic shut off for discontinuing suction when a predetermined volume of fluid has been drained.

Abstract: A tissue closure treatment system and method are provided with an external patient interface. A first fluid transfer component FTC.1 comprises a strip of porous material, such as rayon, with liquid wicking properties. FTC.1 can be placed directly on a suture line for transferring fluid exuded therethrough. An underdrape is placed over FTC.1 and includes a slot exposing a portion of same. FTC.2 comprises a suitable hydrophobic foam material, such as polyurethane ether, and is placed over the underdrape slot in communication with FTC.1. Negative pressure is applied to FTC.2 through a connecting fluid transfer component FTC.3. A negative pressure source can comprises a manual device or a power-operated suction device. The tissue closure method includes a manual operating mode using a manual suction device with an automatic shut off for discontinuing suction when a predetermined volume of fluid has been drained.

Abstract: The present invention is a bolus for an enteral feeding tube, or catheter, that is capable of being used in an over-the-wire intubation procedure as well as other intubation procedures. The bolus has a generally tubular body defining a sidewall, a proximal end tube opening capable of being connected to a distal end of the enteral feeding tube, and a generally rounded terminal end having a flattened tip. The bolus includes a fluid opening within the sidewall of the bolus between the proximal end opening and the terminal end of the bolus. An interior surface of the sidewall opposite the fluid opening is curved and slopes upwardly toward a distal end of the fluid opening. The curved interior surface and the fluid opening configuration allows for fluid flow that approximates the fluid flow rate characteristics of an open-ended tube. The fluid opening is biased toward the terminal end of the bolus thereby defining an elongated collar portion adjacent the proximal end tube opening of the bolus.

Abstract: Disclosed is a medical device used to prevent the cross contamination of patients or injectors.

Abstract: A heart muscle irrigation device comprises a short rivet like member with one closed and one open end, and a barrel including a plurality of holes, slots, an area mesh, or a grid. The irrigation device is inserted into the heart muscle so as to provide a channel from, for example, the left ventricle, to provide an adequate oxygenated blood supply to a starved muscle. The irrigation device is inserted from either outside or inside the rib cage by an insertion device. The insertion device comprises a plunger and barrel assembly adapted to contain the irrigation device. The tip of the insertion device includes members adapted to penetrate the heart muscle. If the irrigation device is inserted through an insertion into the rib cage, an applicator comprising a tubular member with a planar tip including a soft elastomeric seal can be used whereby a portion of the heart muscle is held more or less rigidly for the short period during which the irrigation device is inserted.

Abstract: A safety shield apparatus is disclosed which includes a needle having a distal portion defining a longitudinal axis which is angularly displaced relative to a longitudinal axis defined by a proximal portion of the needle. A shield is mounted with the needle and extensible, via a tubular needle guide movable along the needle, between a retracted position and an extended position. The apparatus may include a needle hub configured to support the proximal portion of the needle. The needle hub can include an appendage which may have at least one opening to facilitate manipulation thereof. A distal end of the shield can be attached to a planar contact surface. The shield may also include a latch engageable with the needle.

Abstract: An infusion system for delivery of therapeutic fluids from a remote source into a patient's body. The system has an infusion assembly, a rotating pivot joint member, a fluid connector assembly, and a sealing assembly retained within the infusion assembly between the housing of the infusion assembly and the rotating pivot joint member. The seal reduces leakage of fluids. The rotating joint may be pivoted to three distinct positions to allow for emplacement on the patient, delivery of the therapeutic fluid to the patient, and protected, sealed closure of the fluid channels to avoid patient fluid backflow.

Abstract: A method and related device for performing sterile medical procedures are disclosed. The method and related device are capable of accessing a sterile environment from a non-sterile environment to perform a medical procedure within the sterile environment. The method and related device can achieve a sterile technique during endoluminal procedures and in uncontrolled and unsterile environments. The device includes an inner hollow member moveably disposed within an outer hollow member. The outer hollow member is adapted to penetrate a boundary separating non-sterile and sterile environments and the inner hollow member is adapted to extend past the outer hollow member and into the sterile environment. A fluid compartment is adapted to be in selective fluid communication with the outer tube such that when the inner member extends past the outer member and into the sterile environment, fluid enters the outer member and the boundary.

Abstract: A splash shield for use in wound irrigation is provided. The splash shield includes at least one outlet area located along its rim so that irrigating fluid may flow from the splash shield. The splash shield is preferably oval-shaped with a substantially flat top adjacent to which is a receiver unit. The outlet area can be formed, for example, by contoured portions or by a generally V-shaped opening, each able to define a channel to enable the escape of fluid from the splash shield. The splash shield may be used in tandem with a syringe having a tip that is positioned in the receiver unit. Additionally, a basin can be provided for use during wound irrigation. The basin includes indentations to accommodate placement of a portion of the human body within the basin and an exit portion such that fluid in the basin can move in the basin to the edge of a table, bed, gurney or the like.

Abstract: A method and related device for performing sterile medical procedures are disclosed. The method and related device are capable of accessing a sterile environment from a non-sterile environment to perform a medical procedure within the sterile environment. The method and related device can achieve a sterile technique during endoluminal procedures and in uncontrolled and unsterile environments. The device includes an inner hollow member moveably disposed within an outer hollow member. The outer hollow member is adapted to penetrate a boundary separating non-sterile and sterile environments and the inner hollow member is adapted to extend past the outer hollow member and into the sterile environment. A fluid compartment is adapted to be in selective fluid communication with the outer tube such that when the inner member extends past the outer member and into the sterile environment, fluid enters the outer member and the boundary.

Abstract: The present invention is a bolus for an enteral feeding tube, or catheter, that is capable of being used in an over-the-wire intubation procedure as well as other intubation procedures. The bolus has a generally tubular body defining a sidewall, a proximal end tube opening capable of being connected to a distal end of the enteral feeding tube, and a generally rounded terminal end having a flattened tip. The bolus includes a fluid opening within the sidewall of the bolus between the proximal end opening and the terminal end of the bolus. An interior surface of the sidewall opposite the fluid opening is curved and slopes upwardly toward a distal end of the fluid opening. The curved interior surface and the fluid opening configuration allows for fluid flow that approximates the fluid flow rate characteristics of an open-ended tube. The fluid opening is biased toward the terminal end of the bolus thereby defining an elongated collar portion adjacent the proximal end tube opening of the bolus.

Abstract: A method and related device for performing sterile medical procedures are disclosed. The method and related device are capable of accessing a sterile environment from a non-sterile environment to perform a medical procedure within the sterile environment. The method and related device can achieve a sterile technique during endoluminal procedures and in uncontrolled and unsterile environments. The device includes an inner hollow member moveably disposed within an outer hollow member. The outer hollow member is adapted to penetrate a boundary separating non-sterile and sterile environments and the inner hollow member is adapted to extend past the outer hollow member and into the sterile environment. A fluid compartment is adapted to be in selective fluid communication with the outer tube such that when the inner member extends past the outer member and into the sterile environment, fluid enters the outer member and the boundary.

Abstract: A needle assembly comprising a needle, a needle hub in which the needle is secured at a distal end portion of the needle hub, a protector having an elongated rod-shaped main body and a needle tip protection part provided on the distal end of the main body for sliding on the needle, and a cylindrical hub cover having an inner channel provided on the distal end of the needle hub. The needle hub and the hub cover each have such a shape as to form a side hole when the needle hub and the hub cover are integrally joined, and the protector main body moves to the distal end or the proximal end while inserted in the side hole.

Abstract: A splash shield for use in wound irrigation comprises a three-dimensional shield member having a peripheral edge and a surface extending from the peripheral edge, the shield member being formed at least in part of flexible and pliant material for selectively shaping the peripheral edge to fit the shape or dimension of a wound, and an adjustable hub extending from the surface of the shield member configured to be circumferentially adjustable to adapt to the fluid end portion of any number and variety of irrigation fluid delivery devices. An attachable drain tube and a splash shield having an attached drain tube for removing fluid from the wound site is also disclosed.

Abstract: Many conventional pharmaceutical articles contain seemingly inert components that come into contact with a pharmaceutically active material during use, which contact substantially reduces the pharmaceutical effectiveness of the pharmaceutically active material. The invention described herein concerns various modifications to these incompatible components, which are effective to diminish the reduction in pharmaceutical effectiveness.

Abstract: In accordance with an embodiment of the invention, a needleless injection apparatus includes a cartridge having a plunger disposed at a rearward end. The cartridge includes an inner portion with a throat at a forward portion and a displaceable outlet valve initially disposed within the cartridge throat. The cartridge further includes a generally outwardly facing surface and a system for selectively providing driving force to drive the plunger in a forward direction. The apparatus also includes a nozzle for receiving the cartridge, the nozzle defining a rearward, cartridge-receiving portion, and having a forward portion terminating in and defining a valve abutment surface with a plurality of channels and an injection orifice.

Abstract: A surgical tool (112, 410) for use in expanding a cannula (10, 150, 250) includes a first leg (114, 414) having a first end (118, 418) engageable with an inner surface (70, 212, 322) of the cannula. A second leg (114, 414) is connected with the first leg (114, 414). The second leg (114, 414) has a second end (118, 418) engageable with the inner surface (70, 212, 322) of the cannula (10, 150, 250). The first and second ends (118, 418) are movable away from each other to apply a radially outwardly directed force to the inner surface (70, 212, 322) of the cannula (10, 150, 250) and cause expansion of the cannula.

Abstract: A tissue traction device according to the invention includes an elongated tube defining a vacuum passageway, which tube has a proximate end defining a first opening, a distal end defining a second opening, and a third opening between the ends. A shield covers the distal end of the tube, the shield having a plurality of openings providing communication between the vacuum passageway and an exterior surface of the shield. The shield prevents the tissue from being pulled deep into the tube, thereby protecting the tissue from damage. Each of the openings having a cross-sectional area smaller than the cross-sectional area of the vacuum passageway. The tube and shield are configured for use in surgery, such that when suction is applied to one of the first and third openings, the level of suction through the second opening can be controlled by varying the extent to which the other of the first and third openings is uncovered, whereby the suction causes the shield to selectively hold tissue against the shield.

Abstract: The female vaginal douche with cervical shield is a unique device with a wide range of health implications. The device is unique because there is no existing device available that offers the ability to cleanse the vaginal mucosa without allowing a forceful flow of fluid, debris, and bacteria (both commensal and pathogenic), into the uterine cervix. At present, when vaginal douching takes place, there is no barrier in place to protect or shield the cervix from this potentially harmful practice. By combining the vaginal douche applicator with an attached cervical shield, access to the uterine cervix will be limited. The limitation theoretically prevents microorganisms from entering the upper female genital tract. Shielding the cervix during vaginal douching has the potential to prevent serious pelvic infections including pelvic inflammatory disease, tuboovarian abscess, endometritis, as well as female factor infertility and potentially life threatening ectopic pregnancy.

Abstract: A heart muscle irrigation device comprises a short rivet like member with one closed and one open end, and a barrel including a plurality of holes, slots, an area mesh, or a grid. The irrigation device is inserted into the heart muscle so as to provide a channel from, for example, the left ventricle, to provide ad adequate oxygenated blood supply to a starved muscle. The irrigation device is inserted from either outside or inside the rib cage by an insertion device. The insertion device comprises a plunger and barrel assembly adapted to contain the irrigation device. The tip of the insertion device includes members adapted to penetrate the heart muscle. If the irrigation device is inserted through an insertion into the rib cage, an applicator comprising a tubular member with a planar tip including a soft elastomeric seal can be used whereby a portion of the heart muscle is held more or less rigidly for the short period during which the irrigation device is inserted.

Abstract: A shaped flexible infusion sleeve provides for delivery of an infusion fluid to the tip of a vibrating needle used in a phacoemulsification procedure for removing cataracts. The shaped flexible infusion sleeve has a non-circular cross-sectional shape which allows deformation yet prevents collapse of the sleeve onto the vibrating needle so as to avoid undesired heating during surgery. The shaped flexible infusion sleeve has at least two constriction points which add sufficient structural sniffiness to prevent full collapse of the sleeve once inserted into an incision in the eye, while at the same time providing sufficient flexibility to enhance sealing of the incision.

Abstract: A pericardiocentesis apparatus and method for accessing the pericardial space. The invention consists of inserting a percutaneous tube whose tip has a hole which is positioned over and contacts the anterior pericardium. Introducing a vacuum within the tube forms a pericardial bleb within that hole. A guided needle within the tube is advanced to puncture the pericardial bleb while avoiding contact with the epicardium. A hollow filament or electrocardial lead or flexible guide wire within the needle can then be advanced into said pericardial cavity. The guide wire may be used to guide a intrapericardial catheter into the pericardial space for injection or infusion of selected therapeutic agents into the pericardial space to treat various heart and blood vessel diseases. Controlled drug release material(s) can be injected through the needle for the slow and/or sustained delivery of the therapeutic agents into the pericardial cavity.

Abstract: The method includes the steps of compressing a carrier to eliminate gas nuclei before exposure of the carrier to the gas; exposing the compressed carrier to the gas under pressure to form a gas-saturated compressed carrier; transporting the gas-saturated compressed carrier to the delivery system; and infusing the gas-saturated compressed carrier from the delivery system at an exit port to the environment without associated bubble formation and cavitation proximate the exit port so that the gas is transported to the site within the environment in solution with the carrier in a supersaturated state, the gas being liberated therefrom remote from the exit port upon arrival at the site within the environment.

Abstract: A tubular implant to be used for percutaneously feeding a patient, which implant is made of resiliently deformable material and includes a distal enlargement adapted to be inserted into the stomach and having at least one opening and a proximally following central tubular section adapted to be inserted into a punctured hole extending from the outside into the stomach cavity, characterized in that the implant includes releasable tensioning or pinching means for reversibly reducing the diameter of the implant along its total length such that it is freely displaceable together with said means through a usual trocar sleeve.

Abstract: A ventilator manifold is disclosed which includes a port for attachment and detachment of an accessory device thereto without interruption of continuous respiratory support of the patient. A particular embodiment of an accessory device described herein includes a suctioning device for removal of fluids from a patient's lungs during respiratory support. The manifold includes an accessory access port which has a normally closed valve therein which remains closed regardless of the pressure changes within the manifold. The normally closed valve is positioned in the port such that insertion of an accessory device adaptor therein forces the normally closed valve to an open position. Removal of the adaptor of the accessory device allows the normally closed valve to return to its closed position, thus allowing continued operation of the respiratory system even when no accessory device is present in the accessory device access port.

Abstract: A flexible, sterile, trimable device which gently and continuously removes unwanted fluid from an operating field during surgery by wicking the fluid into a mat having a high wicking property. A flexible suction tube having one end embedded in the mat removes fluid from the mat, thereby preventing the mat from becoming saturated. One embodiment of the invention is as a surgical swabber where one end of a length of semi-rigid tube is embedded in the mat and the other end is connected to a flexible suction tube. Another embodiment of the invention is as a platform for microsurgery where a membrane having a plurality of holes is applied to one side of the mat. The membrane supports the tissue being worked on and is preferably a contrasting color. Fluid passing into the holes is wicked into the mat where it is subsequently removed by the suction tube. The platform can be oriented in any position and does not slip on the tissue on which it is placed.

Abstract: A selectively aspirating stylet assembly comprises a stylet having proximal and distal ends, the proximal end in fluid communication with a fluid supply and the distal end disposed at or near the end of a catheter, cannula or other generally tubular member that is to be inserted to a specified location within a patient's body, so as to create a fluid flow path from the fluid supply through the generally tubular member to the specified location. A valve assembly located within the fluid flow path is operable to close off a fluid column within the stylet assembly to facilitate placement of the tubular member within the body, and to control the flow of fluids within the assembly.

Abstract: A hollow operating needle for an ultrasonic surgical probe for fragmenting and removing material from the body has an elongated tapered portion which is coupled at its larger end portion to an ultrasonic motor for receiving and transmitting vibrations along the length of the needle to the operating end of the needle, with the needle defining at least one generally rectangular opening extending co-axially from the operating tip end and having the intersections of the longer sides of the at least one opening and the operating tip end being beveled, whereby a substantial portion of irrigating fluid supplied adjacent the operating end portion of the needle reaches the operating tip end of the needle and the surgical site and another substantial portion of the fluid passes through the at least one opening without reaching the operating tip of the needle.

Abstract: A device for the prevention of contamination of medical personnel from a patient's body secretions that may splash back during wound irrigation. The splash shield has a peripheral edge that is substantially circular. The splash shield has a flat center region which forms the middle of the splash shield encircled by an outer concave region. The outer concave region curves away from the flat center region. A peripheral edge is located at the rim of the outer concave region. The peripheral edge is flat and extends outwardly from the outer concave region in a plane substantially parallel to the flat center region. A hollow conical protrusion extends through the splash shield at a point eccentric to its center. The conical protrusion has a base that lays flush against the flat center region. As the conical protrusion extends away from the flat center region, it tapers to a top surface.

Abstract: A vacuum tube tip for use proximate loose tissue. The vacuum tube tip including an elongated tube having a longitudinal axis, a peripheral wall and a distal tip. At least one opening extends through the peripheral wall proximate the distal end. At least one fin is disposed proximate the opening. The fin is operably enacted to the peripheral wall of the tube and extends generally away from the tube. The fin is configured so that when a vacuum is created into the tube through the opening, loose tissue drawn toward the opening is held away from the opening by the fin.

Abstract: The invention relates to a respiratory support system (10) which includes a suction catheter device (41), a suction control valve (36), and a ventilator manifold (11). The ventilator (11) includes an access port (15) for attachment and detachment of the suction catheter device (41) thereto without interruption of continuous respiratory support of the patient. The access port (15) has a normally closed valve (16) therein which remains closed regardless of the pressure changes within the manifold (11). The normally closed valve (16) is positioned in the port (15) such that placement of a specially designed connector (40) of the suctioning device (41) therein forces the normally closed valve (16) to an open position, The manifold (11) and valve (16) are adapted to allow cleaning of the catheter (54) therethrough without detachment thereof.

Abstract: An improved gastrostomy tube is a flexible tube having on one inner end thereof an improved energy absorbent internal retaining member which provides for less patient trauma during emplacement and subsequent percutaneous removal, while almost entirely avoiding either separation of the internal retaining member, i.e., the bumper, or its acute displacement. The energy absorbing internal retaining member has a hollow body portion with two resiliently reversible physical forms or shapes, toroidal-like, and, goblet-like connected to a foreshortened hollow axial stem portion that is attached to or integrally made with the inward end of the flexible tube. The internal retaining member is made in the toroidal-like form. During intentional removal, when under pressure against the stomach mucosa, the internal retaining member snaps into the unrolled, goblet-like shape and pulls smoothly out through the stoma tract.

Abstract: A speculum cover for a speculum blade has a smoke tube associated therewith. The speculum cover may be removable from the blade.

Abstract: An endoscopic suctioning instrument with variable suction is disclosed. The instrument has a hollow cannula having a proximal end and a distal end, and sliding sleeve having a proximal end and a distal end and a longitudinal axis, with the sliding sleeve being coaxial to and closely surrounding and slidingly engaging the hollow cannula. The sliding sleeve has a plurality of lateral holes at its distal end with the lateral holes being spaced along the longitudinal axis.

Abstract: A probe carrying sensor means at its distal tip is supported centrally within a blood vessel by an introducer catheter. The introducer catheter includes a percutaneously insertable shaft which is configured to engage and be supported by the inner luminal surface of the blood vessel. The distal tip of the catheter shaft is disposed along a central axis of the catheter such that when the catheter is disposed in the blood vessel, the distal tip will be disposed substantially along that axis and substantially in the center of the blood vessel lumen. The probe passed through the catheter thus will emerge from the distal outlet orifice of the catheter into the blood vessel at the central axis of the blood vessel.

Abstract: An esophageal gastric tube inserted through the mouth or nose into the stomach of a patient. The single tube incorporates a lumen ending in a stomach catheter to permit necessary evacuation of the stomach contents including a relief passage to admit ambient air pressure to avoid undue stomach contraction. The tube also incorporates a stethoscopic lumen with a pick-up port to be located in the heart lung area of the patient to monitor heart and lung sounds during an on-going operation.

Abstract: A method for removing fatty tissue from a patient includes the steps of inserting an aspirating cannula into the fatty tissue of the body, removing the fatty tissue in the vicinity of an internal layer of the patient's skin and traumatizing the skin adjacent to the area from which fatty tissue is removed. The method is generally carried out by means of an improved aspirating cannula which includes a longitudinally extending tubular member, an opening at one end thereof and a plurality of integrally formed projecting members surrounding the openings. The projecting members are relatively narrow and thin and extend radially outwardly and longitudinally. An annular member which is angularly disposed with respect to the longitudinally projecting member and of similar width and thickness connects the longitudinal members and is effective in breaking down fat tissue without cutting blood vessels or nerves during reciprocal movements of the cannula.

Abstract: A stylet assembly is provided for inserting a catheter into a brain ventricle and providing a cerebrospinal fluid flashback indicia of proper catheter positioning. The stylet assembly includes an elongated, generally cylindrical rigid hollow stylet having an open distal end, a rounded blunt proximal end, and an internal fluid passageway extending the length of the stylet. A relatively large single aperture is provided through the stylet adjacent to its proximal end, for permitting fluid flow into the internal fluid passageway. The aperture is configured to underlie a plurality of catheter inlet apertures and has a width generally corresponding with the diameter of the internal fluid passageway. An elastomeric hub surrounds a portion of the stylet adjacent to the distal end.

Abstract: A method of forming a disposable suction swab from an elongated stem having an enlarged, resilient tip at one end. The stem is installed in a longitudinal central channel in the tip, and the assembly is then compressed between a pair of displaceable clamp plates, the plates having drill apertures in registration with one another and with the tip being in alignment with the apertures. A hole is then bored through the compressed tip and stem by drilling through the apertures in the clamp plates. The plates are released to eject the formed swab.

Abstract: A device for introducing fluids into the lumen of a body duct comprises an elongate shaft having a mechanism at its distal end for capturing the duct. A needle is disposed within an axial passage in the shaft, and a mechanism for reciprocating the needle is located at the proximal end of the shaft. In this way, the duct can be captured with the capture mechanism and pierced with the needle. The fluid is then provided to the lumen of the duct through a perfusion port located at or near the distal end of the needle. Optionally, a mechanism for applying a vacuum externally to the duct within the capture mechanism is provided to help hold the duct and open the interior to facilitate introduction of the fluid.

Abstract: Auxiliary suction equipment for performing a medical operation. A flexible mat partitions off an organ to be operated on from other internal organs, and a suction tube removes blood and body fluid caused by the operation. The insulating qualities of the mat allow the procedure to be performed with the protection of the organ muscle by a local low-temperature method in order to control the metabolism of the organ to be operated on. The mat can be provided with a passage to introduce a fluid for controlling the temperature of the mat surface.

Abstract: A catheter useful in draining cerebrospinal fluid from the ventricles of a brain. The catheter utilizes a series of holes arranged in a helical pattern at the forward or ventricular end portion of the catheter. Exterior grooves may be provided in the ventricular end of the catheter within which the holes are protectively sheltered from contact with surrounding ventricular tissue. The catheter, and particularly its ventricular end, may be capable of elastic elongation upon insertion of a rigid stylet within the catheter, the diameter of the ventricular end portion become reduced in response to its axial elongation to facilitate disengagement of the catheter with the surrounding ventricular tissue to permit the catheter to be withdrawn.