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Unique Device Identification
Results: 463

#	Item
81	[removed]Federal Register / Vol. 70, No[removed]Wednesday, May 25, [removed]Notices information within the meaning of the Freedom of Information Act and FDA’s Add to Reading List Source URL: www.fda.gov Language: English - Date: 2005-05-25 09:03:55 Piperazines Clinical research Food and Drug Administration Cyclopropanes Therapeutics Ciprofloxacin Ofloxacin ClinicalTrials.gov Unique Device Identification Pharmacology Medicine Otologicals
82	Microsoft Word - Dear Non-sterile Ortho Set Labelers[removed]FINAL.doc Add to Reading List Source URL: www.fda.gov Language: English Medical technology Neurosurgery Implants Unique Device Identification Vertebral fixation Medical device Spinal fusion Biomet Title 21 of the Code of Federal Regulations Medicine Orthopedic surgery Prosthetics
83	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire Avenue Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-11-12 10:07:46 Health Center for Devices and Radiological Health Medical device Unique Device Identification Premarket approval Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Dexcom Adverse event Food and Drug Administration Medicine Technology
84	Electronic Medical Device Reporting (eMDR) Basics November 4, 2014 Andrew Xiao Consumer Safety Officer Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Medical device Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Unique Device Identification Food and Drug Administration Medicine Health
85	November 2, 2012 Farzad Mostashari, MD, ScM National Coordinator for Health Information Technology Department of Health and Human Services 200 Independence Avenue, SW Washington, DC 20201 Add to Reading List Source URL: www.healthit.gov Language: English - Date: 2013-01-18 20:42:27 Health informatics Pharmaceutical sciences Medicine GMDN Udi people SNOMED CT Health Food and Drug Administration Unique Device Identification
86	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire Avenue Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-10-24 14:23:34 Health Center for Devices and Radiological Health Premarket approval Medical device Unique Device Identification Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Investigational Device Exemption Food and Drug Administration Medicine Technology
87	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire Avenue Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-10-14 11:52:12 Technology Premarket approval Center for Devices and Radiological Health Medical device Federal Food Drug and Cosmetic Act Unique Device Identification Adverse event Title 21 of the Code of Federal Regulations Institutional review board Food and Drug Administration Medicine Health
88	[removed]Federal Register / Vol. 79, No[removed]Thursday, October 23, [removed]Proposed Rules the Commission’s standards in more specific, codified, and readily accessible Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-10-23 02:41:55 Food and drink Food Safety Modernization Act Rulemaking Federal Food Drug and Cosmetic Act Center for Food Safety and Applied Nutrition Food Safety and Modernization Act Unique Device Identification Food and Drug Administration Health Medicine
89	Girl with shopping bags looking at falling matrix Add to Reading List Source URL: www.gs1.org Language: English - Date: 2014-10-09 10:25:26 Standards organizations Electronic commerce Universal identifiers GS1 Global Data Synchronization Network Unique Device Identification Global Trade Item Number Electronic Product Code International Article Number Identifiers Identification Barcodes
90	FDA’s Home Use Medical Device Initiative Add to Reading List Source URL: www.fda.gov Language: English Technology Unique Device Identification Center for Devices and Radiological Health Medical device Premarket approval Adverse event Title 21 CFR Part 11 Structured Product Labeling Food and Drug Administration Medicine Health

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