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Unique Device Identification
Results: 463

#	Item
91	07.__H130005.A002_APPROVAL_ORDER[removed]pdf Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-08-22 15:51:34 Technology Center for Devices and Radiological Health Federal Food Drug and Cosmetic Act Medical device Title 21 of the Code of Federal Regulations Adverse event Humanitarian Device Exemption Unique Device Identification Food and Drug Administration Medicine Health
92	IMDRF - Meeting 4 Washinton DC, September 2014 outcome statement Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2014-09-30 21:03:40 Asia-Pacific Economic Cooperation Unique Device Identification International relations Economics Food and Drug Administration Research Working group
93	FDA’s Home Use Medical Device Initiative Add to Reading List Source URL: www.fda.gov Language: English Technology Center for Devices and Radiological Health Medical device Federal Food Drug and Cosmetic Act Center for Food Safety and Applied Nutrition Office of Regulatory Affairs Adverse event Unique Device Identification Premarket approval Food and Drug Administration Medicine Health
94	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 16:41:56 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
95	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: 2014-09-02 11:06:04 Technology 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 Health
96	UDI guidance: Unique Device Identification (UDI) of medical devices Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2014-09-01 00:56:15 Automatic identification and data capture Food and Drug Administration Unique Device Identification Medical technology Global Harmonization Task Force Medical device Barcode Radio-frequency identification Technology Medicine Medical equipment
97	G:OCSFIL~1IES~17238.XML Add to Reading List Source URL: www.fda.gov Language: English - Date: 2007-10-11 08:10:14 Pharmacology European Medicines Agency Unique Device Identification Regulation of tobacco by the U.S. Food and Drug Administration Food and Drug Administration Pharmaceutical sciences Clinical research
98	OUTCOME STATEMENT of the IMDRF-6 MANAGEMENT COMMITTEE 16 to 18 September 2014 Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2014-09-30 21:03:40 Asia-Pacific Economic Cooperation Unique Device Identification International relations Economics Food and Drug Administration Research Working group
99	MS_DeviceBarcode01_km_OWN.jpg Add to Reading List Source URL: www.pewtrusts.org Language: English - Date: 2014-07-30 15:27:25 Health informatics Unique Device Identification Pharmaceutical sciences International standards Medical equipment Electronic health record Medical device Adverse event Medicine Health Food and Drug Administration
100	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 16:41:56 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

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