Abstract: A method and system of establishing communications between at least two independent software modules in a safety critical system, such as a medical system, is provided. The design comprises providing an exclusive Bluetooth connection between at least two wireless devices. A master wireless device is configured with Bluetooth master device functionality and a slave wireless device is configured with Bluetooth slave device functionality. The wireless devices are employed in performing a medical procedure. The method further comprises acquiring a stored unique address from the slave wireless device over the Bluetooth connection, comparing the stored unique address to a master wireless device unique address available at the master wireless device, and exclusively pairing the master wireless device and the slave wireless device when the unique address acquired from the slave wireless device is found to identically match the master wireless device unique address.

Abstract: A method and system of establishing communications between at least two independent software modules in a safety critical system, such as a medical system, is provided. The design comprises providing an exclusive Bluetooth connection between at least two wireless devices. A master wireless device is configured with Bluetooth master device functionality and a slave wireless device is configured with Bluetooth slave device functionality. The wireless devices are employed in performing procedures in a safety critical environment. The method further comprises acquiring a stored unique address from the slave wireless device over the Bluetooth connection, comparing the stored unique address to a master wireless device unique address available at the master wireless device, and exclusively pairing the master wireless device and the slave wireless device when the unique address acquired from the slave wireless device is found to identically match the master wireless device unique address.

Abstract: Methods and devices measure eye blinks and tear film lipid and aqueous layer thickness before and following ophthalmic formula application onto the ocular surface, especially wherein the ophthalmic formula is an artificial tear. The methods and devices are suitable for dry eye diagnosis. The methods and devices are suitable for use to evaluate ophthalmic formula effects on the tear film and to use such information to diagnose ophthalmic formula treatment of ocular disease conditions such as dry eye in the absence of contact lens wear or post-surgical eye drop treatment and diagnosis. The methods and devices are also suitable for use in the optimization of ophthalmic drug dosage forms and sustained drug release.

Abstract: Implantation of an accommodating intraocular lens in an eye may require the accurate measurement of the size, circumference, or diameter of the capsular bag of the eye. After the natural crystalline lens has been surgically removed, a flexible ring may be temporarily or permanently inserted into the capsular bag for measuring the circumference of the capsular bag. The ring is generally compressible to fit through a surgical incision, then expands to fill the capsular bag along an equatorial region. The ring has a central component that changes shape as the ring is compressed. The shape change is generally correlated to the size of the capsular bag and may be measured visually or with a camera through the cornea, the measurement being generally independent of corneal magnification.

Abstract: The present embodiments relate to a novel method of making quaternary ammonium polymers comprising the steps of: a) mixing 1,4-bis-dimethylamino-2-butene, triethanolamine, water and an acid; and b) introducing a 1,4-dihalo-2-butene to the mixture so as to initiate a reaction resulting in the quaternary ammonium polymer.

Abstract: A method and system of controlling access to a system in a medical environment is provided. The method includes calculating a signature value for at least one file usable with the medical system, transferring the calculated signature value to a signature file, and providing at least one signature value in the signature file and at least one associated file to a file system configured to be received by the medical system. At least one signature value and at least one associated file are inspected by the medical system to verify the associated file is a known medical software application asset. The medical system comprises an input/output data port configured to receive the external memory storage device, and an operating system capable of reading medical system data from and writing medical system data to the memory storage device.

Abstract: A method and apparatus of controlling access to a system containing vital corporation software and storing confidential data assets situated in an open accessible environment is provided. The method includes calculating a signature value for at least one file usable with the system, transferring the calculated signature value to a signature file, and providing at least one signature value in the signature file and at least one associated file to a file system configured to be received by the system. At least one signature value and at least one associated file are inspected by the system to verify the associated file is a known system software application asset. The system comprises an input/output data port configured to receive the external memory storage device, and an operating system capable of reading system data from and writing system data to the memory storage device.

Abstract: An intraocular lens system includes a primary intraocular lens configured to correct vision in a patient, and a supplemental intraocular lens configured to modify the correction provided by the primary intraocular lens. The supplemental intraocular lens, which is substantially completely diffractive, is preferably ultrathin. The two lenses may be connected to, or separate from, one another. The supplemental intraocular lens may be implanted at the same time as the primary intraocular lens, or added later.

Abstract: An alignment tool for a laser beam delivery system includes a base having one or more registration elements and an alignment optic operably coupled to the base. The alignment optic has a fluorescent element and a front surface. The fluorescent element is configured to fluoresce when illuminated by electromagnetic radiation produced by a laser. The front surface includes a reflective surface and an alignment mark. The reflective surface is configured to specularly reflect the electromagnetic radiation, while the alignment mark, which is centrally disposed within the reflective surface, is configured to diffusely scatter the electromagnetic radiation.

Abstract: An intraocular lens is disclosed, with an optic that changes shape in response to a deforming force exerted by the zonules of the eye. A haptic supports the optic around its equator and couples the optic to the capsular bag of the eye. The haptic may be pre-stressed before the optic is placed within it. After such placement, the pre-stress may be relieved, and the haptic may produce stress in the optic. The pre-stress may produce a radial tension or a radial compression in the optic. Alternatively, once the optic is placed within the haptic, both may undergo a process that changes the size and/or shape of one with respect to the other, causing a stress within the optic. This process may produce a radial tension or a radial compression in the optic. The haptic may include an annular ring having outer and inner diameters that may depend on the stiffness of the haptic.

Abstract: An intraocular lens is disclosed, with an optic that changes shape in response to a deforming force exerted by the zonules of the eye. A haptic supports the optic around its equator and couples the optic to the capsular bag of the eye. The region of contact between the optic and the haptic extends into the edge of the optic, similar to the interface between a bicycle tire and the rim that holds it in place. The haptic may be stiffer than the optic. The haptic may have the same refractive index as the optic. The haptic may include a saddle-shaped portion in contact with the adjustable optic, with a convex profile along an optical axis; and a concave profile in a plane perpendicular to the optical axis.

Abstract: A multi-zonal monofocal opthalmic lens comprises an inner zone, an intermediate zone, and an outer zone. The inner zone has a first optical power. The intermediate zone surrounds the inner zone and has a second optical power that is different from the first power by a magnitude that is less than at least about 0.75 Diopter. The outer zone surrounds the intermediate zone and has a third optical power different from the second optical power. In certain embodiments, the third optical power is equal to the first optical power.

Abstract: The invention is generally directed to systems and methods for fluid control, and more particularly to systems and methods for power and flow rate control for aspiration. In accordance with one embodiment, an aspiration system includes an aspiration line having distal and proximal ends and an aspiration port defined in the distal end; a fluid transport device operatively coupled to the proximal end of the aspiration line; and a flow restrictor operatively coupled to the aspiration line in between the fluid transport device and the aspiration port. To measure occlusion within the line, first and second pressure sensors are utilized, the first sensor being operatively coupled to the aspiration line between the port and the restrictor and the second sensor being operatively coupled to the aspiration line between the restrictor and the fluid transport device. The pressure differential between the two sensors can provide an indication of the onset, presence, and/or elimination of an occlusion.

Abstract: A multi-purpose contact lens care solution having high activity against fungi and certain bacteria comprising, in liquid aqueous medium, an alkylamine having the following formula, where R1 is a C13-17 alkylamine, and R2 and R3 are each independently H or —CH3, and a non-ionic surfactant. The solution may optionally also include additional antimicrobial components, a buffer component, a viscosity inducing component, a surfactant, taurine, propylene glycol and/or a tonicity component. This solution additionally prevents losses in ocular tissue membrane integrity during contact lens wear.

Abstract: Test apparatus for bi-manual phaco needle apparatus are provided which includes a chamber for establishing a fluidic circuit between an irrigation needle and an aspiration needle. A first inlet into the chamber is provided for establishing a sealed communication with the irrigation needle and a second inlet is provided for establishing a sealed fluid communication with an aspiration needle. The apparatus enables a method for testing bi-manual phacoemulsification apparatus and priming thereof.

Abstract: An eye treatment cassette includes a handpiece, a vacuum source, a holding tank, a collection bag, and a displacement-based pump. The handpiece is configured to aspirate fluids from a patient's eye. The vacuum source communicates with the handpiece. The holding tank is interposed between the handpiece and the vacuum source, and is configured to hold the aspirated fluids. The collection bag is connected to the holding tank for collecting the aspirated fluids. The pump is coupled to the holding tank and is configured to operate while the vacuum source continues to aspirate fluids via the handpiece to drain the aspirated fluids from the holding tank.

Abstract: An eye treatment system includes an eye treatment probe and a console. The console has a cassette receptacle and a fluid drive system including a first peristaltic drive rotor and a second peristaltic drive rotor. The first and second drive rotors are exposed to the receptacle and are substantially coaxial. The cassette includes a cassette body and a fluid pathway network for coupling the fluid drive system of the console with the probe. The cassette body has cassette positioning surface for fittingly engaging the receptacle. The fluid pathway network has a first resilient tubing segment and a second resilient tubing segment, the first and second tubing segments are configured for peristaltic driving engagement by the first and second rotors, respectively, when the cassette is mounted to the console. Various elements of the cassette are configured for interfacing with the components of the console when the cassette is mounted to the console.

Abstract: A method and system of establishing communications between at least two independent software modules is provided. The design comprises providing a media connection between software modules, wherein the software modules employ a communications protocol and participate in a bi-directional master-slave relationship between a master module and a slave module. The design further comprises sending arbitrary data between the master and slave modules, wherein the arbitrary data is used by the master module to control and obtain status from the slave module, and sending arbitrary data further enables the slave module to return data and status information to the master module. The design also employs a communications watchdog between the master and slave modules, wherein the communications watchdog monitors communications quality between the master and slave modules and impairs functionality in the master and slave modules when communications quality degrades.

Abstract: A sterile drape maintains a sterile field during use of a flat panel touch screen during diagnostic and/or therapeutic procedures. The drape comprises sterile front and rear sheets formed from a thin layer of a transparent material that accommodates the transmission of tactile pressure. The rear sheet may comprise a folded extension of the front sheet along the top edge, with the sheets bonded along the sizes. A bottom opening between the front and the rear sheets allows cooling air to enter, and at least one ventilation opening is near the top.

Abstract: A method and system for calibrating an analog sensor used in a digital measurement system is provided. The design comprises generating a precise pressure value set at multiple calibration points and supplying said precise pressure value set to an uncalibrated pressure sensor, detecting sensor changes for the uncalibrated pressure sensor based on each precise pressure value generated, polling an actual pressure reading associated with a sensor change for the uncalibrated pressure sensor for each calibration point, and establishing a mathematical relationship between measured value readings and actual pressure for the uncalibrated sensor. Establishing the mathematical relationship converts the uncalibrated sensor to a newly calibrated sensor. A known good sensor may be employed to enhance calibration reliability.