Diagnostic System definition

Diagnostic System means an ePlex System or an eSensor System.
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Examples of Diagnostic System in a sentence

  • For the Worldwide Diagnostic System (WDS) Ford Motor Company is purchasing an ( ) System, modified to meet Ford vehicle interface requirements, which can provide Ford Dealers with a single worldwide diagnostic tool and the software required to use the tool to service Ford vehicles.

  • As Vice President of Business Development for Diagnostic System Laboratories she was responsible for business expansion through evaluation and implementation of new growth opportunities and patent portfolio management.

  • The company's technology platform is the Given(R) Diagnostic System, featuring the PillCam video capsule, a disposable, miniature video camera contained in a capsule, which is ingested by the patient.

  • OTHER NON-DEVELOPED TECHNOLOGY (ONDT) REFERENCE ID # TITLE COMMENTS International Patent Application No. PCT/US99/20646 Multi-Modal Optical Cancer Diagnostic System ONDT limited [*] All other technology and concepts proprietary to SpectRx only.

  • In support of this objective the primary hypothesis was that, in patients being evaluated for known, suspected or risk of cardiac arrhythmias, the presence of TWA measured during an exercise stress test using the spectral method of the CH 2000 Cardiac Diagnostic System and Hi Res(TM) ECG electrodes was predictive of increased susceptibility to ventricular arrhythmias.

  • This patent application entitled Automated Infrared Printed Circuit Board Failure Diagnostic System was filed as a provisional application on April 18, 2002 at the USPTO.

  • INTRODUCTION 7.1. DEVICE INFORMATION 7.1.1. The CH 2000 The CH 2000 Cardiac Diagnostic System received FDA 510(k) clearance on February 29, 1996 (510(k) Number K950018).

  • The Technical Support Group provides the following categories of Technical Support to the airline customer: - Product Support Engineering - Powerplant Maintenance Engineering - Customer Performance Engineering - Diagnostic System Engineering - Human Engineering - Flight Operations Engineering - Repair Services - Field Operations Data Analysis PRODUCT SUPPORT ENGINEERING Product Support Engineering is responsible for the overall technical support to the customers.

  • The Company is, among other things, engaged in the business of developing, manufacturing and distributing the LuMax(TM) Incontinence Diagnostic System product line including a variety of surgical and diagnostic instruments and accessories, as more specifically described on Exhibit A hereto (the "Business").

  • August 20, 1998 8 The secondary objective of the study was to demonstrate that, in patients being evaluated for known, suspected or risk of cardiac arrhythmias, the presence of TWA measured during an exercise stress test using the spectral method of the CH 2000 Cardiac Diagnostic System and Hi Res(TM) ECG electrodes was substantially equivalent to or better than the SAECG measured using the ART (Arrhythmia Research Technology, Inc.), LP-Pac Q(TM) ver.

Related to Diagnostic System

  • Diagnostic x-ray system means an x-ray system designed for irradiation of any part of the human or animal body for the purpose of diagnosis or visualization.

  • Diagnostic Service means an examination or procedure performed to obtain information regarding the medical condition of an outpatient.

  • Diagnostic Services means services provided for the purpose of determining the nature and cause of a condition, ill- ness, or injury.

  • Diagnostic source assembly means the tube housing assembly with a beam-limiting device attached.

  • Diagnostic mammography means a method of screening that

  • Therapeutic school means a residential group living facility:

  • Diagnostic Product means In Vitro Diagnostics, In Vivo Diagnostic Agents and any product used for Diagnosis.

  • in vitro diagnostic medical device means any medical device which is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, equipment, software or system, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue donations, derived from the human body, solely or principally for the purpose of providing information:

  • Gene Therapy means the introduction of a nucleic acid sequence encoding a protein intended for or otherwise conferring therapeutic benefit into a person for therapeutic purposes (i) by in vivo introduction for incorporation into cells of such person, or (ii) by ex vivo introduction into cells for transfer into a person.

  • Vaccine means a specially prepared antigen which, upon administration to a person, will result in immunity and, specifically for the purposes of this rule, shall mean influenza and pneumococcal vaccines.

  • Clean coal technology demonstration project means a project using funds appropriated under the heading “Department of Energy—Clean Coal Technology,” up to a total amount of $2,500,000,000 for commercial demonstration of clean coal technology, or similar projects funded through appropriations for the Environmental Protection Agency. The federal contribution for a qualifying project shall be at least 20 percent of the total cost of the demonstration project.

  • Analytical x-ray system means a group of components utilizing x-rays to determine the elemental composition or to examine the microstructure of materials.

  • Bioassay means the determination of kinds, quantities or concentrations and, in some cases, the locations of radioactive material in the human body, whether by direct measurement, in vivo counting, or by analysis and evaluation of materials excreted or removed from the human body. For purposes of these rules, “radiobioassay” is an equivalent term.

  • Software Product means any COTS which you propose to provide pursuant to the contract.

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Biomarker means a parameter or characteristic in a patient or Patient Sample, the measurement of which is useful (a) for purposes of selecting appropriate therapies or patient populations or monitoring disease susceptibility, severity or state, or monitoring therapies for such patient and/or (b) for predicting the outcome of a particular treatment of such patient.

  • Qualified high-technology business means a business that is either of the following:

  • Licensed System means, collectively:

  • Companion Diagnostic means a device which is essential for the safe and effective use of a corresponding medicinal product to:

  • Developed Software means software specifically designed for the Principal under the Contract. Depending how advanced its development is, it may be either a Product or a Service or both.

  • Medical marijuana product means a product that contains cannabinoids that have been extracted from plant material or the resin therefrom by physical or chemical means and is intended for administration to a licensed patient, including but not limited to concentrates, oils, tinctures, edibles, pills, topical forms, gels, creams, and other derivative forms, except that this term does not include live plant forms.

  • Hemp products means all products made from industrial hemp,

  • Commercial Software means Software developed or regularly used that: (i) has been sold, leased, or licensed to the general public; (ii) has been offered for sale, lease, or license to the general public; (iii) has not been offered, sold, leased, or licensed to the public but will be available for commercial sale, lease, or license in time to satisfy the delivery requirements of this Contract; or (iv) satisfies a criterion expressed in (i), (ii), or (iii) above and would require only minor modifications to meet the requirements of this Contract.

  • Software Products and “Software” are interchangeable and mean software, computer source codes and other computer programs.

  • Program Materials means the documents and information provided by the Program Administrator specifying the qualifying EEMs, technology requirements, costs and other Program requirements, which include, without limitation, program guidelines and requirements, application forms and approval letters.

  • Research Use shall have the meaning given in Section 2.2.2 of this Agreement.