Health / Medical Topics

    FDA Device Listing Number

    Definition 1

    A number assigned by the FDA to a device during Registration and Listing. (NCI Thesaurus)

    Definition 2

    Number assigned by FDA during Registration and Listing to all devices in commercial distribution, regardless of pre-market authorization requirements, per 21 CFR 807.28(f). See 21 CFR 807 for all Registration and Listing requirements. (Food and Drug Administration)




    YOU MAY ALSO LIKE

    The class of medical device as determined by the US Food and Drug Administration, based upon the level of control necessary to…
    Sterilization methods that do not have a long history of safe and effective use and for which there are no FDA-recognized standards,…
    Terminology used in individual case reports for voluntary and mandatory reporting of adverse reactions or adverse events during both pre and post…
    A set of terminology created to support the efforts of the FDA CDRH Global Unique Device Identification Database project.
    A written regulatory communication from FDA to an applicant, who submitted request to the agency to approve marketing or to license medical…
    Terminology codelist used to describe the principal observations for human clinical and non-human non-clinical studies for the FDA CDA guide.

    © 1991-2023 The Titi Tudorancea Bulletin | Titi Tudorancea® is a Registered Trademark | Terms of use and privacy policy
    Contact