Boehringer Mannheim Gmbh

Careside, Inc.

Roche Diagnostics Gmbh

Roche Diagnostics Operations, Inc.

Acterna LLC

Gds Technology, Inc.

David E Storvick

Daniel L Kennedy

Charles L Thomeczek, Jr

James R Parker

Rick L Collins

William J Murphy

Gary T Neel

Morris J Young

George R Lennert

Richard A Riedel

Roger Hammer

Michael E Grant

John Stoughton

Dino Perin

Glen Mathews

Russell T Gray

James J Ramey

James S Hutchinson

Mark A Gregory

James D Morrow

Douglas E Boyd

John W Stoughton

Surendra K Gupta

James S Hutchison

William J Mclaughlin

Martin T Gerber

Aurora F De Castro

William R Boyd

Steven R Arbuckle

Stephen D Scopatz

Brett S Lewis

Peter L Sebastian

William O Reid, Jr

William Reid

Darrin L Paugh

Friedrich Jost

Aurora F Decastro

The invention provides a handheld RF meter with an improved isolation from EMI. The meter incorporates an interference barrier comprising a connecting cable and one or more ferrite cores possibly having different impedance characteristics.

RF meter with input noise suppression

In combination, an instrument for determining a characteristic of a biological fluid or a control, and a cuvette for holding a sample of the biological fluid or control, the characteristic of which is to be determined. The instrument comprises a radiation-reflective surface, a first source for irradiating the surface, and a first detector for detecting radiation reflected from the surface. The cuvette has two opposed walls substantially transparent to the source radiation and reflected radiation. The first source and first detector are disposed adjacent a first one of the two opposed walls. The radiation reflective surface is disposed adjacent a second of the two opposed walls. A second source is provided for irradiating the surface. The first detector detects radiation from the second source reflected from the surface. The second source is positioned to transmit radiation through the two opposed walls for reflection by the surface and transmission back through the two opposed walls to the first detector to indicate whether a sample has reached a first point in the cuvette.

Fluid dose, flow and coagulation sensor for medical instrument

An analytical instrument for analyzing fluids. The instrument includes a cartridge carousel assembly which receives analytical cartridges. The cartridges are self-contained units which incorporate a sample metering/separation system which is operated by centrifugal force. The cartridge carousel is composed of a cartridge rotor plate which includes a center and a plurality of cartridge ports which are located in spaced relation radially outward from the center of the plate. The analytical instrument further includes an optical detector which measures a detectable analytical property of the fluid sample which is provided by the optical element of the cartridge. The optical detector includes a radiation source which shines a beam of radiation on the optical element. The optical detector further includes a return beam detector which measures the return beam of radiation emitted by the optical element. The radiation source and return beam detector are both located on the same side of the cartridge rotor plate. The analytical instrument includes a tracking and control unit which tracks and controls the rotary drive mechanism and the detector to provide coordinated operation so that the optical detector can make measurements of the optical element while the cartridge rotor is stationary or rotating.

Cartridge-based analytical instrument with optical detector

The instrument includes a cartridge carousel assembly which receives analytical cartridges. The cartridges are self-contained units which incorporate a sample metering/separation system which is operated by centrifugal force. The cartridge carousel is composed of a cartridge rotor plate which includes a center and a plurality of cartridge ports which are located in spaced relation radially outward from the center of the plate. The cartridge ports include a cartridge dock which is shaped to receive the cartridges and a balance weight dock which is located radially inward from the cartridge dock. The cartridge dock is shaped to receive a balance weight. A locking mechanism is provided which holds the cartridge in the cartridge dock during rotation of the cartridge rotor plate. A balancing mechanism is provided which includes a balance weight which is movable to the balance weight dock when a cartridge is inserted into the cartridge dock. An ejection mechanism is provided which ejects the test cartridge from the cartridge port after processing of the test cartridge is completed.

Cartridge-based analytical instrument with rotor balance and cartridge lock/eject system

An analytical instrument for analyzing fluids. The instrument includes a cartridge carousel assembly which receives analytical cartridges. The analytical cartridges include a centrifugal force-operated sample metering/separation system, a pressure-operated sample transport system, and a test element which provides a detectable analytical property of a fluid sample. The cartridge carousel assembly includes a cartridge rotor plate which has a plurality of cartridge ports which receive the cartridges. A rotary drive mechanism rotates the cartridge rotor plate to provide rotation of the plate which activates the centrifugal force-operated sample metering/separation system of the cartridge. The instrument includes a sample transport actuator which activates the pressure-operated sample transport system of the cartridge. In addition, the instrument includes a detector which measures the detectable analytical property of the fluid sample after the sample metering and transport systems have been activated. The instrument includes tracking and control systems which track and control the rotary drive mechanism and sample transport actuator to provide coordinated operation of the centrifugal force-operated sample metering/separation system and the pressure operated sample transport system wherein the coordinated operation provides delivery of a metered amount of sample to the test element of the test cartridge. Further, the tracking and control unit includes a user-input interface for receiving data input from a user of the instrument, a central processing unit, a real-time processor, and a data output interface which provides output of results of the measurements made by the instrument.

Cartridge-based analytical instrument using centrifugal force/pressure for metering/transport of fluids

An instrument for determining a characteristic of a biological fluid or a control includes a radiation-reflective surface, a first source for irradiating the surface, and a first detector for detecting radiation reflected from the surface. A cuvette for use with the instrument holds a sample of the biological fluid or control the characteristic of which is to be determined. The cuvette has two opposed walls substantially transparent to the source radiation and reflected radiation. The first source and first detector are disposed adjacent a first one of said two opposed walls and the radiation reflective surface is disposed adjacent a second of said two opposed walls.

An instrument monitors the coangulation of coagulable fluid blood, blood fraction or a control by combining the coagulable fluid with particles which are affected by a magnetic field so that the particles become suspended relatively freely in the fluid. A time-varying magnetic field causes the particles to be reoriented as the magnetic field varies. The reorientation changes as the fluid coagulates owing to the fluid's changing viscosity. An electromagnet creates the time-varying magnetic field. The electromagnet includes a core comprising a first leg an electrically conductive coil for creating a time-varying magnetic flux in the core, and a return for the time-varying magnetic flux. The first leg and the flux return together comprise a generally H-shaped core of ferromagnetic material. A bobbin is provided on the first leg and the electrically conductive coil is wound on the bobbin.

Magnet for medical instrument

An instrument and a method for determining a characteristic of a biological fluid or control comprise providing a radiation-reflective surface, a source for irradiating the surface, a detector for detecting radiation reflected from the surface, and a cuvette for holding a sample of the biological fluid or control. The cuvette has two opposed walls substantially transparent to the source radiation and reflected radiation. The source and detector are disposed adjacent a first one of the two opposed walls and the radiation reflective surface is disposed adjacent the other wall. The method comprises detecting radiation from the source reflected from the surface using the radiation detector to determine a characteristic of the biological fluid or control.

A method of immunizing the operation of an instrument which determines a characteristic of a biological fluid or a control against noise. The instrument includes a surface upon which a user deposits a sample of biological fluid or control the characteristic of which is to be determined. The instrument irradiates the sample and detects radiation from the sample to determine the characteristic. The method comprises monitoring the detected radiation a first time to determine if the detected radiation is increasing or decreasing, forming a first change in detected radiation from said first monitoring, subsequently monitoring the detected radiation a second time to determine if the detected radiation is increasing or decreasing, forming a second change in detected radiation from said second monitoring, forming an overall change in detected radiation from the first and second monitorings, establishing a first threshold, establishing a second threshold, comparing the first change to the first threshold, comparing the second change to the first threshold, if the magnitudes of both the first and second changes are greater than the first threshold, comparing the overall change in radiation to the second threshold, and determining the characteristic if the magnitudes of the first and second changes are greater than the first threshold and the overall change is greater than the second threshold.

A method of determining whether a sample or a control has been applied to an instrument for measuring coagulation of a fluid by optically detecting when the fluid that has been applied to the instrument has passed a first and a second points, determining the flow time for the fluid between the two points, establishing a time threshold, and the flow time to the threshold to determining if the fluid is a sample or a control.

Fluid dose flow and coagulation sensor for medical instrument

An instrument and a method for determining a coagulation characteristic of blood, a blood fraction or a control comprise a radiation-reflective surface, a first source for irradiating the surface, and a first detector for detecting radiation reflected from the surface. A cuvette holds a sample of the blood, blood fraction or control the coagulation characteristic of which is to be determined. The cuvette has two opposed walls substantially transparent to the source radiation and reflected radiation. The first source and first detector are disposed adjacent a first one of the two opposed walls and the radiation reflective surface is disposed adjacent a second of the two opposed walls.

Combined blood coagulation measuring instrument and test strip

A method and apparatus (10) for determining the remission of a chemistry (106) which reacts with a medically significant component of a body fluid. The remission of the chemistry (106) changes as it reacts. The method and apparatus (10) include irradiating the chemistry (106) with a radiation source (182), detecting remissions of radiation from the chemistry (106) with a radiation detector (300), providing a radiation pathway (164) between the source (182) and the chemistry (106), providing a remission pathway (164) between the chemistry (106) and the detector (300), and detecting the rate of change of remission of the chemistry (106) with respect to time. The irradiating, detecting and rate detecting steps and apparatus comprise initially irradiating the chemistry (106) at a first time rate and detecting remissions therefrom, comparing remission data from remission readings spaced apart by a first number of intervening remission readings, and determining when the difference between compared readings exceeds a first predetermined limit. The time rate of irradiation of the chemistry is changed once the difference between compared readings exceeds the first limit. Remission data from remission readings spaced apart by a second number of intervening remission readings are then compared. The method and apparatus next determine when the difference between compared readings no longer exceeds a second predetermined limit. The last remission reading is then converted to the concentration of the medically significant component of the body fluid.

Apparatus and method for analyzing a body fluid

An instrument for analyzing test strips supporting chemistries which react with a medically significant component of a body fluid to indicate the concentration of the component in the body fluid. The instrument includes a pathway along which radiation is guided from a radiation source to a strip when the strip is inserted into the instrument and along which remission is guided from the strip to a radiation detector. A title provided on the instrument provides a first remission when no strip is inserted into the instrument. The tile is separated from the radiation source by the strip when the strip is inserted into the instrument. The first remission and the strip's remission, respectively, indicate the absence and the presence of the strip in the instrument. The strip also has a surface opposite the chemistry supporting surface characterized by a second strip remission different from the first strip remission. The instrument is capable of determining whether the strip has been inserted into the instrument correctly or backward.

Test strip holding and reading mechanism for a meter

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Indianapolis, IN, United States of America

David E Storvick