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Unique Device Identification
Results: 463

#	Item
231	Public Health Service DEPARTMENT OF HEALTH & HUMAN SERVICES Food and Drug Administration[removed]New Hampshire Avenue Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:11:22 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 Medicine Food and Drug Administration Technology
232	Food and Drug Administration DEPARTMENT OF HEALTH & HUMAN SERVICES[removed]New Hampshire Avenue Silver Spring, MD 20993 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:10:39 Health Premarket approval Center for Devices and Radiological Health Medical device Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Unique Device Identification Investigational Device Exemption Food and Drug Administration Medicine Technology
233	Federal Register / Vol. 69, No[removed]Tuesday, June 1, [removed]Notices project, and their applicability to policy and practice. The provision of a detailed discussion of the objectives and of the extent to which they are Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2010-12-01 23:14:23 Technology Medical device Validation Center for Devices and Radiological Health Center for Biologics Evaluation and Research Title 21 of the Code of Federal Regulations Title 21 CFR Part 11 Unique Device Identification Medicine Food and Drug Administration Health
234	[removed]Federal Register / Vol. 72, No[removed]Wednesday, December 19, [removed]Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Add to Reading List Source URL: www.fda.gov Language: English - Date: 2007-12-19 08:14:22 Pharmaceutical sciences Federal Food Drug and Cosmetic Act Premarket approval Center for Biologics Evaluation and Research New Drug Application Center for Devices and Radiological Health FDA Warning Letter Unique Device Identification Food and Drug Administration Medicine Health
235	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire Avenue Document Control Room -WO66-G609 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:10:53 Health Center for Devices and Radiological Health Premarket approval Medical device 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
236	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire Avenue Silver Spring, MD 20993 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:11:43 Technology Medical device Center for Devices and Radiological Health Premarket approval Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Unique Device Identification Medicine Food and Drug Administration Health
237	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration[removed]New Hampshire Avenue Document Control Room -W066-G609 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:10:41 Health Premarket approval Center for Devices and Radiological Health Medical device Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Unique Device Identification Investigational Device Exemption Food and Drug Administration Medicine Technology
238	DEPARTMENT OF HEALTH & HUMAN SERVICES Food and Drug Administration[removed]New Hampshire Avenue Document Mail Center - W066-G609 Silver Spring, MD[removed] Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:10:50 Health Center for Devices and Radiological Health Premarket approval Medical device Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Unique Device Identification Investigational Device Exemption Food and Drug Administration Medicine Technology
239	DEPARTMENT OF HEALTH & HUMAN SERVICES Food and Drug Administration[removed]New Hampshire Avenue Silver Spring, MD 20993 Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:12:01 Health Premarket approval Center for Devices and Radiological Health Medical device Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Unique Device Identification Investigational Device Exemption Food and Drug Administration Medicine Technology
240	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: 2013-12-06 12:10:34 Health Center for Devices and Radiological Health Premarket approval Medical device 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

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