Device Alert definition

Device Alert has the meaning given to that expression in the DCC User Interface Specification. Device and User System Tests has the meaning given to that expression in Section H14.31 (Device and User System Tests).
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Device Alert has the meaning given to that expression in the DCC User Interface Specification.
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Device Alert has the meaning given to ‘Alert’ in the GB Companion Specification. Device and User System Tests has the meaning given to that expression in Section H14.31 (Device and User System Tests).
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Examples of Device Alert in a sentence

  • When the stored Command is executed at the specified future dated execution date and time an Alert is sent to confirm the Commands execution (which is sent to the relevant User as a Device Alert).

  • The User shall ensure that its Receive Response Service sends a synchronous Acknowledgement to the DCC following the User’s receipt of each Service Response, Device Alert or DCC Alert.

  • On November 13, 2009 the U.S. Food and Drug Administration (FDA) released a Medical Device Alert regarding the use of negative pressure wound therapy systems.

  • On November 13, 2009, the U.S. Food and Drug Administration (FDA) released a Medical Device Alert regarding the use of negative pressure wound therapy systems.

  • DCC Alert means an alert generated in the DCC Total System (with the exception of any Device Alert generated) which is to be sent to a relevant User(s) depending on the alert, in the format specified in clause 3.6.3. DCC Scheduled means a mode of operation in which a Service Request is to be generated and processed by the DCC on behalf of the User at regular intervals for future times as specified in the Service Request.

  • Medical Device Alert ref MDA/2009/080: Ultrasound transducer probes with an internal lumen used for taking transrectal prostrate biopsies.

  • Device Alert means either a communication in the format set out in clause 3.6.2 containing an Alert as defined by GBCS, generated by a Device, or a SMETS1 Alert, which (in either case) is to be sent to a User.

  • It is especially important for protection from discrimination, violence, abuse and exploitation, and for ensuring their best interests in all actions involving or having an impact on them...”.

  • The Agency will sometimes issue a Medical Device Alert (MDA) warning of hazardous products, potential safety issues or unsafe procedures, and providing relevant advice.

  • Medical Device Alert: ASRTM hip replacement implant manufactured by DePuy International Ltd.

Related to Device Alert

  • Step therapy protocol means a protocol or program that establishes the specific

  • Therapeutic school means a residential group living facility:

  • Quality system means documented organizational procedures and policies: internal audits of those policies and procedures: management review and recommendation for quality improvement.”

  • Devices means any and all devices owned or purchased from time to time by Party A and utilized for the purposes of the provision of the Services.

  • 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:

  • Device means each of a computer, workstation, terminal, handheld PC, pager, telephone, personal digital assistant, “smart phone,” server or any other hardware where software can be installed that would allow End User to interact with the Product.

  • API means American Petroleum Institute.

  • Radiopharmaceutical quality assurance means, but is not limited to, the performance of appropriate chemical, biological, and physical tests on potential radiopharmaceuticals and the interpretation of the resulting data to determine their suitability for use in humans and animals, including internal test assessment, authentication of product history, and the keeping of proper records.

  • Veterinarian means a veterinarian authorized by law to practice veterinary medicine in this State.

  • Diagnostic clinical procedures manual means a collection of written procedures that describes each method (and other instructions and precautions) by which the licensee performs diagnostic clinical procedures; where each diagnostic clinical procedure has been approved by the authorized user and includes the radiopharmaceutical, dosage, and route of administration.

  • Tobacco product manufacturer means an entity that after the date of enactment of this Act directly (and not exclusively through any affiliate):

  • 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.

  • Manufacturing Process means any process for—

  • Manufacturing means all activities related to the manufacture of a Compound, including planning, purchasing, manufacture, processing, compounding, storage, filling, packaging, waste disposal, labeling, leafleting, testing, quality assurance, sample retention, stability testing, release, dispatch and supply, as applicable.

  • Prescription device means an instrument, apparatus, implement, machine,