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Unique Device Identification
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111	Federal Register / Vol. 77, No[removed]Monday, May 21, [removed]Notices ebenthall on DSK5SPTVN1PROD with NOTICES Transcripts: Please be advised that as soon as a transcript is available, it will Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2013-05-23 10:58:13 Medicine Food Safety Modernization Act Validation Center for Food Safety and Applied Nutrition Unique Device Identification Food Safety and Modernization Act Food and Drug Administration Pharmaceutical sciences Health
112	FDA’s Regulatory Tutorials Online and Webpage Navigation Add to Reading List Source URL: www.fda.gov Language: English Medicine Food Safety and Modernization Act Center for Food Safety and Applied Nutrition Unique Device Identification Food and Drug Administration Health Pharmaceutical sciences
113	asabaliauskas on DSK5VPTVN1PROD with NOTICES Federal Register / Vol. 79, No[removed]Wednesday, October 8, [removed]Notices 5:30 p.m., and Thursday, November 20, 2014, from approximately 8:30 a.m. to 12:45 p.m. Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-10-08 12:12:15 Pharmaceutical sciences Pharmaceuticals policy National Institutes of Health Therapeutics United States Public Health Service Prescription Drug User Fee Act Unique Device Identification Food and Drug Administration Modernization Act Food and Drug Administration Medicine Health
114	DEPARTMENT OF HEALTH & HUMAN SERVICES April 10, 2014 Public Health Service Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-08-13 16:39:39 Health Medical device Premarket approval Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Investigational Device Exemption Unique Device Identification Food and Drug Administration Medicine Technology
115	Agenda for Quarterly Meeting on MDUFA III (FY[removed]Performance July 30, [removed]:00 A.M. Welcome. Barbara Zimmerman, CDRH-ODE. Guidance Development Add to Reading List Source URL: www.fda.gov Language: English Technology Premarket approval Center for Devices and Radiological Health Medical device Investigational Device Exemption Federal Food Drug and Cosmetic Act Center for Biologics Evaluation and Research Unique Device Identification Food and Drug Administration Medicine Health
116	NWX HHS FDA (US) Moderator: Irene Aihie[removed]:30 am CT Confirmation # [removed]Page 1 Add to Reading List Source URL: www.fda.gov Language: English Health informatics Unique Device Identification Medical device Health Level 7 Center for Devices and Radiological Health GMDN Medicine Health Food and Drug Administration
117	Agenda for Quarterly Meeting on MDUFA III (FY[removed]Performance November 5, [removed]:00 A.M. Welcome. Barbara Zimmerman, CDRH-ODE. Guidance Development Add to Reading List Source URL: www.fda.gov Language: English Technology Premarket approval Center for Devices and Radiological Health Unique Device Identification Medical device Investigational Device Exemption Federal Food Drug and Cosmetic Act Center for Biologics Evaluation and Research Title 21 CFR Part 11 Food and Drug Administration Medicine Health
118	DEPARTMENT OF HEALTH & HUMAN SERVICES April 10, 2014 Public Health Service Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-08-13 16:40:33 Health Medical device Premarket approval Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Investigational Device Exemption Unique Device Identification Food and Drug Administration Medicine Technology
119	DEPARTMENT OF HEALTH & HUMAN SERVICES April 10, 2014 Public Health Service Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-08-13 16:40:55 Health Medical device Premarket approval Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Investigational Device Exemption Unique Device Identification Food and Drug Administration Medicine Technology
120	Attachment E CDRH Final Guidance Cover Sheet Add to Reading List Source URL: www.fda.gov. Language: English Health Unique Device Identification Medical device Federal Food Drug and Cosmetic Act Center for Devices and Radiological Health Quality management system Radio-frequency identification Food and Drug Administration Medicine Technology

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