Abstract: Catheterization apparatus for implanting devices is provided with a device tether. The apparatus includes a device delivery tube that provides a pathway for moving implant devices through a patient's vasculature to internal body cavities. The implant devices are carried or pushed through the device delivery tube by a tubular push rod. The implant devices are tethered to a line passing through the push rod lumen. After deployment, the implant devices may be retracted into the device delivery tube for repositioning or retrieval by pulling on the tether.

Abstract: A skin pricker has a housing (1) for a lancet (5) which, when released from a rearward cocked position, is propelled forwards by a spring momentarily to project its tip (3). During the forward motion a peg (12) within the housing (1) passes along a slot (10) in the lancet and, just before the tip (3) projects, snaps through a neck (11) at the rear end of the slot. If the lancet (5) is then pushed back, the peg (12) cannot re-enter the slot (10): instead it wedges the lancet sideways and, before it can be re-cocked, traps the lancet behind an abutment (13) ensuring that the tip (3) cannot be re-exposed.

Abstract: A suture shuttle in the form of a loop of flexible metallic material, such as nitinol wire, is disclosed. The flattened loop of nitinol wire is long enough to extend into an arthroscopic portal and out an accessory portal through a joint undergoing arthroscopic surgery. After installing a suture anchor in bone, a strand of suture attached to the suture anchor is retrieved through the accessory portal. Using a cannulated instrument having a sharp tip, the tissue to be repaired is pierced to create an opening. The nitinol loop is deployed through the cannulated instrument and passed through the opening. The retrieved suture strand is placed through the portion of the nitinol loop and pulled through the tissue opening before arthroscopic knots are tied.

Abstract: An apparatus used with a helical suture device has a first end and a second end. The first end includes a spatulate member having a length along a first axis. The second end includes a guide shaped to receive a cylindrical axle of the helical suture device for rotation on a second axis. The guide is shaped to constrain the first axis in fixed position relative to the second axis, the first and second axes each lying within a plane. The spatulate member extends, typically symmetrically, in a first direction and a second direction from the first axis, the first direction and second direction being on opposite sides of the plane. The apparatus lies between a first tissue that is to be sutured, and a second tissue that is desired not to be sutured.

Abstract: The rear end of a dual lumen oocyte recovery needle is sealed in a plastics hub by means of two polyurethane seals compressed between the outside of the needle and opposite ends of a bore through the hub. The needle has an outer tube and an inner tube with a suction lumen along its length and which is deformed to provide a flushing lumen between its outside and the inside of the outer tube. A suction tube is joined to the rear end of the needle at the rear end of the hub in communication with the suction lumen. A flushing tube is joined in a side bore opening into the interior of the hub and communicating via a slot in the side of the needle with the flushing lumen.

Abstract: The invention provides a method of manufacturing a system for treating a vascular condition. A catheter including an inflatable balloon is provided. A stent is positioned over the balloon. An adhesive material is applied between an inner surface of the stent and an outer surface of the balloon. The adhesive material is heated to above a melting point of the adhesive material. The adhesive material is cooled to below a melting point of the adhesive material to provide an adhesive bond that retains the stent to the catheter during vascular delivery, wherein the stent is released from the balloon following inflation and deflation of the balloon at a treatment site.

Abstract: A multiple dose delivery device for delivering a medicament into an oral cavity of a patient is provided. The device includes a sachet pack including a plurality of unit doses of a medicament enclosed between a first strip and a second strip. The device further includes a sachet advance mechanism and a mouthpiece. Upon actuation by a user, the sachet advance mechanism, which is engaged with the sachet pack, separates the first strip from the second strip to release one of the plurality of the unit doses from the sachet pack. The mouthpiece includes an opening, and each released unit dose passes through the opening.

Abstract: An inhaler, comprising an electrohydrodynamic comminution means, a means for partially or fully discharging the liquid comminution and a conduit through which the liquid comminution is administered, wherein the discharging means is arranged to be activated by inhalation of the user.

Abstract: A method and apparatus for reducing the thickness of arterial walls is disclosed. Ablation of the exterior layer of the arterial walls is performed using mechanical or laser ablation techniques. Surveying is preferably carried out during the procedure to ensure optimal ablation. The ablation reduces the effective thickness of the arterial walls and increases flexibility so that the walls distend under normal blood pressure, thereby improving blood flow. Advantageously, the procedure is carried out without invasion of the blood vessel lumen and without damage to the inner layer of the artery wall.

Abstract: A device for controlling the breathing gas flow is provided including a breathing gas block (2), a cover (4) and a valve plate (3) as well as a heating device. Condensation effects are prevented from occurring with the supply of the smallest possible amount of energy by provision of a heating foil (16) as a heating element.

Abstract: A combination mouthpiece for inhalation therapy devices, having a body (1) defining an aerosol duct (2) through which, in use, a stream of air carrying an aerosolized drug is supplied to a patient during inspiration, an inlet hole (4) through the body for receiving in a releasable and secure manner an oxygen tube adapter (5), characterised by at least one partition (6) within the body (1) defining at least one oxygen duct (3), the oxygen duct being in a form such that it extends generally parallel with the aerosol duct (2) and has a flow cross-section sized in order to guide a suitably large oxygen stream from the oxygen tube adapter (5) through the inlet hole (4) to the patient.

Abstract: A device for reducing dead space in a ventilator system has a first tube connectable to the dead space in the ventilator system for producing a flow path for the transport of gas from dead space in the ventilator system, a suction device connected to the first tube for generating an adjustable negative pressure in the first tube, a second tube connectable to dead space in the ventilator system, for producing a flow path for the transport of gas to dead space in the ventilator system, a pump connected to the second tube for generating an adjustable positive pressure in the second tube, and a control unit which regulates the suction device and the pump. The suction device and the pump are formed by a first chamber and a second chamber, respectively, in an enclosure, separated by a gas-tight, moving partition. The control unit regulates the moving partition to regulate the suction device and the pump for achieving simpler and more reliable operation.

Abstract: An actuator is used to dispense a medicament from a container having at least a first and second portion. The actuator includes a holder, a trigger member and a push member. The trigger member is pivotally connected to the holder at a pivot axis. The push member is connected to the trigger member. The push member is adapted to move at least the second portion of the container relative to the holder as the push member is pivoted in a first direction. In one preferred embodiment, the trigger member follows a path, and a stop member engages one of the container and push member and immobilizes the push member as the trigger member is moved along a predetermined portion of the path.

Abstract: An improved therapy for both clearing the blood of unwanted carbon monoxide and anaesthetic chemicals and for rapidly re-oxygenating blood suffering from carbon monoxide poisoning or smoke inhalation. It also includes a therapy delivery device for carbon dioxide and oxygen metering and mixing apparatus for gases under pressure particularly for respirators and medical devices which has a plurality of compressed gas supply lines which are connected to a mixing device for delivery into a demand regulator (respirator or face mask). It includes a gas selection device, an automatic shut off of the carbon dioxide, a purging system, metering of the gases and a mixing chamber to promote a homogeneous mixture of gases and sized for field use by emergency care operators. The therapy is a mixture of carbon dioxide and oxygen for promoting the rapid oxygenation of the patient's blood supply for cases of carbon monoxide poisoning, smoke inhalation or other cases where the blood oxygen level is low.

Abstract: A delivery device (20, 22) for and a method of delivering a substance to the nasal airway (1) of a subject, in particular the posterior region of the nasal airway, the delivery device comprising: a closure unit for causing the closure of the oropharyngeal velum of the subject; and a delivery unit for delivering a gas flow entraining a substance to one of the nostrils of the subject at such a driving pressure as to flow around the posterior margin of the nasal septum and out of the other nostril of the subject, wherein the delivery unit comprises a nosepiece (30, 40, 58, 82, 102, 132) which includes an outlet through which the gas flow is in use delivered to the one nostril and a sealing member for sealing the one nostril to the outlet such as in use to prevent the escape of the gas flow through the one nostril.

Abstract: A compression element and a retention assembly using the compression element to retain an article on a flexible substrate are disclosed. Also disclosed is a method of making an assembly including an article retained on a substrate by a compression element. The retention assembly, compression element and method provide replacements for, e.g., mechanical staples. The retention assemblies, compression elements and methods are particularly useful for attaching elastic articles to the surfaces of flexible substrates without piercing the substrate. One example of attaching an elastic article to the surface of a flexible substrate is the attachment of an elastic strap to a respirator.

Abstract: An aerosol generator includes a housing, a heater and a mouthpiece wherein the heater volatilizes liquid material within a flow passage and forms an aerosol in the mouthpiece. Mixing ambient air with the vaporized liquid material controls a droplet size of the aerosol. The ambient air can be directed into the mouthpiece by at least one air passageway in an airflow entrainment control member. The at least one air passageway provides a desired volume and/or velocity of ambient air entering into the mouthpiece thereby achieving a desired droplet size distribution of an aerosol. In an alternative arrangement, a funnel shaped airflow entrainment control member includes a narrow end proximate the outlet end of the flow passage. A cone angle of the funnel-shaped member can be selected to provide a desired volume of ambient air which mixes with the vaporized liquid material and achieves a desired aerosol droplet size distribution.

Abstract: An aerosol generator includes a fluid passage arranged between a first and a second layer wherein the first and second layers at least partially define the fluid passage. A liquid supply is arranged to provide a fluid in liquid phase to the fluid passage. The aerosol generator also includes a heater arranged to volatilize the fluid in the fluid passage. An outlet of the aerosol generator is arranged to receive the volatilized fluid and direct the volatilized fluid out of the fluid passage. The aerosol generator can be used to generate aerosols containing medicated materials.

Abstract: A portable oxygen concentrator system adapted to be readily transported by a user includes a rechargeable energy source and a concentrator powered by the energy source. The concentrator converts ambient air into concentrated oxygen gas for the user and includes a plurality of adsorption beds and a rotary valve assembly. The rotary valve assembly is relatively rotatable with respect to the plurality of adsorption beds to provide valving action for selectively transferring fluids through the plurality of adsorption beds for converting ambient air into concentrated oxygen gas for the user. The ratio of adiabatic power to oxygen flow for the concentrator is in the range of 6.2 W/LPM to 23.0 W/LPM.

Abstract: A therapeutic aid for providing therapeutic vapors to a child having cold symptoms. The therapeutic aid includes a body member having a perimeter wall. The perimeter wall defines an interior space. The perimeter wall of the body member has a slot positioned along a front portion of the body member whereby the slot is for permitting access to the interior space of the body member. A treatment member is insertable into the interior space of the body member. The treatment member is designed for emitting therapeutic vapors through the body member for easing the cold symptoms of the child when the body member is positioned in a proximity to the child.