Device Alert definition

Device Alert has the meaning given to that expression in the DCC User Interface Specification.
Sample 1Sample 2
Device Alert has the meaning given to ‘Alert’that expression in the GB CompanionDCC User Interface Specification. has the meaning given to that expression in Section H14.31 (Device and User System Tests).
Sample 1
Device Alert has the meaning given to ‘Alert’ in the GB Companion Specification. Device and User System Tests
Sample 1

Examples of Device Alert in a sentence

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

  • Complete the research and draft of report by the end of October 2019.

  • Note: Block Data, Send Device Alert, Send MDM Alert, Send Email Alert options are enabled once the value for the threshold is entered.

  • MHRA: Medical Device Alert MDA/2006/001: Reporting Adverse Incidents and Disseminating Medical Device Alerts: 2006www.mhra.gov.uk 5.

  • Any grant monies received for the purposes described in Section 3(a) hereof shall be applied to reduce the general obligations of the City incurred in connection with the cost of the improvements.

  • The guidance has incorporated the findings of the 2012 HFS study, the recommendations from the MHRA Medical Device Alert, the evidence from a full systematic literature review on the decontamination of SIUPs and the expert opinion of the Endoscopy and Primary Care Working Group and the HAI Reusable Medical Devices Expert Advisory Steering Group.

  • Medical Device Alert: Hip disease - metal on metal hip resurfacing.

  • The NIAIC issues three types of alert – Medical Device Alert, Estate and Facility Alert and a Northern Ireland Alert.

  • In accordance with the Medical Device Alert (MDA/2010/002), there must be a weekly program of inspection of all ward mattresses.

  • Cancels the audible portion of all patient relatedalarms for 60 seconds (does not silence Device Alert).

Related to Device Alert

  • Dialysis solution means either the commercially available, unopened, sterile solutions whose

  • 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 instruments, apparatus, and contrivances, including their components, parts, and

  • API means the American Petroleum Institute.

  • Consumables and medical devices means (consumables) items that require regular replacement (e.g. batteries) to keep a medical device (such as a hearing aid) operational. Many medical devices require consumables.

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

  • 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.

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

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

  • Medical cannabis pharmacy means the same as that term is defined in Section 26-61a-102.

  • 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.

  • 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.

  • Cannabis wholesaler means any licensed person or entity that purchases or otherwise obtains, stores, sells or otherwise transfers, and may transport, cannabis items for the purpose of resale or other transfer to either another cannabis wholesaler or to a cannabis retailer, but not to consumers.

  • Manufacturing Process means any process for—

  • Product Manufacturer means the entity that assembles the component parts to manufacture the final Product;

  • Detailed manufacturing or process data means technical data that describe the steps, sequences, and conditions of manufacturing, processing or assembly used by the manufacturer to produce an item or component or to perform a process.

  • Mobile Devices means battery-operated, handheld electronic personal communication devices, such as, or similar to, cellular telephones, smart phones, PDAs, or pagers, including such devices that are primarily marketed for purposes other than playing electronic games, even if such devices incorporate game-playing functionality, such as, or similar to, Apple’s iPhone or Research In Motion’s Blackberry.

  • 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.

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

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Prescription device means an instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent, or other similar or related article, and any component part or accessory, which is required under federal or state law to be prescribed by a practitioner and dispensed by or through a person or entity licensed under this chapter or exempt from licensure under this chapter.