Unique Device Identification - PDFSEARCH.IO - Document Search Engine

Unique Device Identification
Results: 463

#	Item
241	DEPARTMENT OF HEALTH AND HUMAN SERVICES Display Dab Food and Drug Administration Publication Date Add to Reading List Source URL: www.fda.gov Language: English - Date: 2007-12-18 07:04:29 Clinical research Center for Biologics Evaluation and Research Unique Device Identification FDA Warning Letter Food and Drug Administration Medicine Pharmaceutical sciences
242	Public Health Service DEPARTMENT OF HEALTH & HUMAN SERVICES Nick Lewis M.Sc., RAC (US) Regulatory Affairs Manager Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2012-07-11 11:28:55 Health Medical device Center for Devices and Radiological Health Premarket approval 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
243	0p 4 DEPARTMENT OF HEALTH & HUMAN SERVICES Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-05 19:49:38 Technology 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 Investigational Device Exemption Unique Device Identification Food and Drug Administration Medicine Health
244	OF HEALTH & HUMAN SERVICES 4-CDEPARTMENT SEP[removed] Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:11:02 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 Investigational Device Exemption Unique Device Identification Food and Drug Administration Medicine Technology
245	[removed]Federal Register / Vol. 72, No[removed]Wednesday, September 12, [removed]Notices DEPARTMENT OF HEALTH AND HUMAN SERVICES Add to Reading List Source URL: www.fda.gov Language: English - Date: 2007-09-12 08:04:56 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
246	DEPARTMENT OF HEALTH & HUMAN SERVICES MAY[removed]Public Health Service Food and Drug Administration Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2011-06-02 10:40:22 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
247	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: 2012-06-20 14:51:20 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
248	P100040 Device: Valiant Thoracic Stent Graft with the Captivia Delivery System Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:11:20 Technology Center for Devices and Radiological Health Premarket approval Medical device Federal Food Drug and Cosmetic Act Aneurysm Title 21 of the Code of Federal Regulations Adverse event Unique Device Identification Medicine Food and Drug Administration Health
249	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 12:11:15 Technology 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 Health
250	DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-05 18:21:15 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

UPDATE