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Unique Device Identification
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#	Item
381	FOR IMMEDIATE RELEASE September 26, 2013 Contact: Cynthia McKee[removed] Add to Reading List Source URL: mdic.org Language: English - Date: 2013-09-27 15:18:29 Technology Medical technology Pharmacology Medical equipment Center for Devices and Radiological Health Medical device Unique Device Identification Medicine Food and Drug Administration Health
382	Center for Devices and Radiological Health Add to Reading List Source URL: www.fda.gov Language: English Center for Devices and Radiological Health Medical device Premarket approval Jeffrey Shuren Global Harmonization Task Force Patient safety Unique Device Identification Medicine Food and Drug Administration Health
383	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Health Medical device Center for Devices and Radiological Health Title 21 of the Code of Federal Regulations Laser Title 21 CFR Part 11 Unique Device Identification Medicine Food and Drug Administration Technology
384	PDF Document Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-07-15 09:35:02 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
385	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Health Medical device Center for Devices and Radiological Health Title 21 of the Code of Federal Regulations Laser Title 21 CFR Part 11 Unique Device Identification Medicine Food and Drug Administration Technology
386	PDF Document Add to Reading List Source URL: www.fda.gov Language: English Pharmaceutical sciences Center for Devices and Radiological Health Title 21 of the Code of Federal Regulations Abbreviated New Drug Application Documentation Title 21 CFR Part 11 Unique Device Identification Food and Drug Administration Medicine Health
387	[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 09:02:46 Food and Drug Administration Clinical pharmacology Therapeutics United States Public Health Service Ofloxacin ClinicalTrials.gov Unique Device Identification Pharmaceutical sciences Clinical research Pharmacology
388	INSERT EVENT (AND AGENDA ITEM NUMBER, IF APPROPRIATE)] Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-07-08 11:38:04 Clinical research Pharmaceutical industry Food and Drug Administration Pharmacology Medical equipment Medical device Patient safety Unique Device Identification European Medicines Agency Medicine Health Technology
389	Microsoft Word - P890003s285a001.Letter.Appr.doc Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-05-06 11:11:30 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
390	Microsoft Word - P890003s285a001.Letter.Appr.doc Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-05-06 11:11:30 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

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