Device Model definition

Device Model means a software model of a specific target architecture device or family of devices used for modeling the internal behavior and programming interfaces of the device(s). Device Models provided by Wind River are considered “Software” under the terms of this Agreement.
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Device Model means, in respect of a Communications Hub or a Device (other than a Communications Hub Function or a Gas Proxy Function), the Manufacturer, the model, the hardware version and the firmware version of the Communications Hub or Device.
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Device Model means a grouping of similar ROBD devices made by one manufacturer, vendor, and/or service provider (e.g. CC-ROBD), that are applicable to the same vehicle(s) makes and models, and applicable to the same OBD protocol(s).
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Examples of Device Model in a sentence

  • The date within the draft timetable upon which it is proposed to decommission any particular Requesting Party shall be no earlier than twelve months after the date upon which the SMETS1 Eligible Product Combinations is updated by the DCC so as to include an entry for each of the Device Model combinations contained within each Group that pertains to that Requesting Party.

  • Prior to making such a determination, and with the exception of the SMETS1 ESME Device Model component(s) of the DMC(s) for FOC (as further set out in Clauses 13.10 to 13.12), the DCC shall discuss its proposals with stakeholders and set out the rationale for its selection.

  • Such notifications shall be via the reports produced pursuant to Clause 16.1. In the case of FOC, with the exception of references in Clauses 13.3 to 13.11 references in the Code to DMCs selected for use in Migration Test Phases or SIT Test Phases shall be deemed to include the SMETS1 ESME Device Model components from time to time chosen by the DCC pursuant to this Clause 13.

  • ESD stress levels were performed in compliance with the following JEDEC standards with the results indicated below:• Charged Device Model (CDM), based on JEDEC Specification JESD22-C101, passed at ±500 V• Human Body Model (HBM), based on JEDEC Specification JESD22-A114, passed at ±1500 VNOTE:According to industry research publications, ESD-CDM testing results show better correlation to manufacturing line and field failure rates than ESD-HBM testing.

  • In the case of FOC, with the exception of references in Clauses 13.3 to 13.11 references in the Code to DMCs selected for use in Migration Test Phases or SIT Test Phases shall be deemed to include the SMETS1 ESME Device Model components from time to time chosen by the DCC pursuant to this Clause 13.

  • This Clause 13.4 and Clauses 13.5 to 13.9 do not apply in respect of the SMETS1 ESME Device Model component(s) of the DMC(s) for FOC (as to which see Clauses 13.10 to 13.12).

  • Prior to making such a determination, and with the exception of the SMETS1 ESME Device Model component(s) of the DMC(s) for FOC (as further set out in Clauses 13.10 to 13.12), the DCC shall discuss its proposals with stakeholders and set out the rationale for its selection.This Clause 13.4 and Clauses 13.5 to 13.9 do not apply in respect of the SMETS1 ESME Device Model component(s) of the DMC(s) for FOC (as to which see Clauses13.10 to 13.12).

  • Device Model.....................................................................................

  • An OEM for use in a Customer Device Model for a U.S. Service Provider that either (a) prior to the date this Order is issued, selects the relevant SOCs for use in a Customer Device Model, or (b) has a Legacy Service Provider Contract and, prior to the expiration of that contract, selects the relevant SOCs for use in a Customer Device Model.

  • Q.Ouyang, H.Wang, S.Mudanai, S.Khan, M.Manassian, A.Tasch, C.Maziar and S.Banerjee, “Representative Deep Submicron MOS Device Structures for Device Model and Device Simulator Evaluation,” SRC TECHCON, 1998.


More Definitions of Device Model

Device Model means a unique number or name given to portable test equipment that is made by a device manufacturer.
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Related to Device Model

  • Licensed Software includes error corrections, upgrades, enhancements or new releases, and any deliverables due under a maintenance or service contract (e.g., patches, fixes, PTFs, programs, code or data conversion, or custom programming).

  • Assay means a laboratory analysis of Crude Petroleum to include the following: A.P.I. Gravity, Reid vapor pressure, composition, pour point, water and sediment content, sulfur content, viscosity, distillation, hydrogen sulfide, flash/boiling point and other characteristics as may be required by Carrier.

  • 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.

  • 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.

  • Supplier Software means software which is proprietary to the Supplier or its Affiliates which is used or supplied by the Supplier in the provision of the Services; Supplier Staff means all persons employed or engaged by the Supplier together with the Supplier's servants, agents, suppliers, consultants and Sub-Contractors (and all persons employed by any Sub-Contractor together with the Sub-Contractor’s servants, consultants, agents, suppliers and Sub-Contractors) used in the performance of its obligations under this Contract; Time and Materials means the pricing mechanism for the Services as may be agreed by the Parties and set out at paragraph Error: Reference source not found in the SOW; TUPE means the Transfer of Undertakings (Protection of Employment) Regulations 2006 (SI 2006/246) as amended or replaced or any other regulations or UK legislation implementing the Acquired Rights Directive; Velocity means the Metric which measures the total number of Story Points for Stories that have been accepted in a Sprint, indicating the rate of progress towards Acceptance of all Stories from the Product Backlog;

  • Open-Source Components means any software component that is subject to any open-source copyright license agreement, including any GNU General Public License or GNU Library or Lesser Public License, or other obligation, restriction or license agreement that substantially conforms to the Open Source Definition as prescribed by the Open Source Initiative or otherwise may require disclosure or licensing to any third party of any source code with which such software component is used or compiled.

  • Accelerator-produced material means any material made radioactive by a particle accelerator.

  • Licensed Technology means the Licensed Know-How and Licensed Patents.

  • Customer Technology means Customer's proprietary technology, including Customer's Internet operations design, content, software tools, hardware designs, algorithms, software (in source and object forms), user interface designs, architecture, class libraries, objects and documentation (both printed and electronic), know-how, trade secrets and any related intellectual property rights throughout the world (whether owned by Customer or licensed to Customer from a third party) and also including any derivatives, improvements, enhancements or extensions of Customer Technology conceived, reduced to practice, or developed during the term of this Agreement by Customer.

  • Antibody means a molecule or a gene encoding such a molecule comprising or containing one or more immunoglobulin variable domains or parts of such domains or any existing or future fragments, variants, modifications or derivatives thereof.

  • Drug Substance means an active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body, but does not include intermediates used in the synthesis of such ingredient.

  • Clinical Data means the information concerning the safety or performance that is generated from the use of a device and that are sourced from the following:

  • Third Party Software means software which is proprietary to any third party (other than an Affiliate of the Contractor) which is or will be used by the Contractor for the purposes of providing the Services.

  • Computer software means computer programs, source code, source code listings, object code listings, design details, algorithms, processes, flow charts, formulae, and related material that would enable the software to be reproduced, recreated, or recompiled. Computer software does not include computer databases or computer software documentation.