Medrad, Inc.

Bayer Healthcare LLC

Bayer Medical Care Inc.

John A Brosovich

Michael J Yanniello

Kevin P Cowan

Mark Trocki

Alan D Hirschman

David A Mishler

Barry Iddon

Arthur E Uber, Iii

Edward J Rhinehart

Barry Tucker

Martin J Uram

Edward P Liscio

Richard A Riggio

David M Griffiths

John Francis Kalafut

George J Misic

William J Monski

Albert John Yarzebinski

Sridhar R Balasubramanian

Mo Shuen Ng

Frederick P Windham

Systems and methods for intelligently delivering fluid to a targeted tissue are described. The systems and methods may include directing a pump to distribute fluid to a targeted tissue and receiving one or more signals from an intracorporeal sensing system, where the one or more signals correspond to one or more sensed feedback parameters at the targeted tissue. The systems and methods may also include determining whether the one or more sensed feedback parameters are within an acceptable range. If the one or more sensed feedback parameters are not within the acceptable range, the systems and methods may include determining an adjusted velocity for the plunger necessary to adjust the pressure of the fluid in the pump so that the one or more sensed feedback parameters move within the acceptable range and directing the pump to distribute the fluid at the adjusted velocity.

Medical fluid injector

Provided is a method of collecting and managing information relating to medical diagnostic procedures which includes collecting objective information about a plurality of procedures and subjective information about the results of those procedures. The objective information provides information about the parameters of the procedure and the patient who underwent the procedure while the subjective information includes an assessment of the quality of the results of the procedure. This information can be stored in a database. The database can be accessed and the information therein used in connection with understanding the results of past procedures and planning for future procedures.

Methods and techniques for collecting, reporting and managing ionizing radiation dose

A syringe for use with a powered injector to inject a fluid into a patient that includes a length of material adapted to transmit or propagate electromagnetic energy therethrough. The length of material includes at least a first indicator positioned along the length of material. The first indicator is adapted to interact with at least a portion of the energy being propagated through the length of material in a manner that is detectable. The presence (or absence) of the first indicator provides or corresponds to information about the syringe configuration. The indicator(s) of the present invention can, for example, provide information about syringe configuration by the number and/or position thereof. A plurality or set of such syringes can be provided, with the configuration of each such syringe being represented by the presence or absence of indicator(s) of that syringe.

Encoding and sensing of syringe information

Systems and methods for intelligently delivering fluid to a targeted tissue. The systems and methods may include directing a pump to distribute fluid to a targeted tissue and receiving one or more signals from an intracorporeal sensing system, where the one or more signals correspond to one or more sensed feedback parameters at the targeted tissue. The systems and methods may also include determining whether the one or more sensed feedback parameters are within an acceptable range. If the one or more sensed feedback parameters are not within the acceptable range, the systems and methods may include determining an adjusted velocity for the plunger necessary to adjust the pressure of the fluid in the pump so that the one or more sensed feedback parameters move within the acceptable range and directing the pump to distribute the fluid at the adjusted velocity.

A battery charger system, for use with an injector system, comprises a power supply and a battery pack. The power supply converts AC power to DC power. The battery pack includes a battery and a charging module. The module monitors the operating mode of the injector system. When the battery pack is disconnected from the injection control unit, the module enables the power supply to charge the battery with DC power. When the battery pack is connected to the injection control unit: (A) upon detecting the injector system in an idle mode, the module routes DC power from the power supply to both the battery for charging thereof and the injection control unit for operation thereof; and (B) upon detecting the injector system in a non-idle mode, the module prevents the power supply from charging the battery and enables the battery to provide DC power to the injection control unit.

Continuous battery charger system

A syringe for use with a powered injector to inject a fluid into a patient inclides an encoder. The encoder includes at least a first indicator positioned on the encoder. The first indicator is adapted to interact with at least a portion of energy being propagated through or adjacent the encoder in a manner that is detectable. The presence (or absence) of the first indicator provides or corresponds to information about the syringe configuration. The indicator(s) of the present invention can, for example, provide information about syringe configuration by the number and/or position thereof. A plurality or set of such syringes can be provided, with the configuration of each such syringe being represented by the presence or absence of indicator(s) of that syringe.

Injector with continuous battery charger system

An antenna coupling enables communication across a barrier to radio frequencies. The antenna coupling comprises first and second antennas. The first antenna is adapted for positioning on a first side of the barrier, and is capable of receiving from and transmitting to a first transceiver disposed on the first side. The second antenna is adapted for positioning on a second side of the barrier, and is capable of receiving from and transmitting to a second transceiver on the second side. The interconnection of the first and second antennas through the barrier comprises the antenna coupling. The antenna coupling enables the first and second transceivers to communicate across the barrier over the desired range(s) of radio frequencies. In a related aspect, the antenna coupling may also include a filter interconnected between the first and second antennas to prevent radio frequencies outside of the desired range(s) from being transmitted across the barrier.

Communication systems for use with magnetic resonance imaging systems

An apparatus and method is provided for improving the quality of electrocardiogram (ECG) signals obtained from a patient undergoing magnetic resonance imaging (MRI) wherein the ECG signal has relatively high levels of noise or interference voltages induced on it by changing magnetic fields. The apparatus includes the arrangement of a differential amplifier, a prefilter, a signal limiter (SL) circuit and an intermediate amplifier with an integral low pas filter. The prefilter limits the rise time or high frequency component of the noise or interfering voltages induced on the ECG that are presented to the signal limiter.

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Pittsburgh, PA, United States of America

John A Brosovich