Back to Results
First PageMeta Content
Unique Device Identification / National Drug Code / Data Universal Numbering System / Medical device / Title 21 CFR Part 11 / Structured Product Labeling / Validation / Health Level 7 / Federal Food /  Drug /  and Cosmetic Act / Medicine / Food and Drug Administration / Health


Attachment B CDRH Draft Guidance Cover Sheet
Add to Reading List

Document Date: 2014-06-25 15:47:45


Open Document

File Size: 2,78 MB

Share Result on Facebook

City

Rockville / /

Company

Dun & Bradstreet / UDI Work Group / /

/

Event

Credit Rating / /

IndustryTerm

software solution/tool / certain medical devices / biological products / public search / food supply / tobacco products / manufacturing practice requirements / software version number / diagnostic products / stand-alone software / medical device products / healthcare services / combination products / cellular and tissue-based products / /

MedicalTreatment

dietary supplements / radiation / /

Organization

U.S. Department of Health and Human Services / HL7 / office of Communication / Outreach and Development / Food and Drug Administration / DUNS / FDA ACCREDITED ISSUING AGENCY / i.e. / Center for Devices and Radiological Health / FDA ESG / GMDN Agency / Division of Dockets Management / Food and Drug Administration Center for Devices / European Commission / GUDID DI / Center for Biologics Evaluation and Research / Center for Devices and Radiological Health Center for Biologics Evaluation and Research / Labeler Organization / /

Person

Silver Spring / /

/

Position

GUDID Coordinator / contractor / Governor / responsible official / Coordinator / Each Coordinator / /

Product

Final Rule / /

ProgrammingLanguage

XML / /

ProvinceOrState

Maryland / /

Technology

radiation / XML / extensible markup language / /

URL

http /

SocialTag