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Unique Device Identification
Results: 463

#	Item
271	Identifying Real-world Human Factors Issues Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Food and Drug Administration Unique Device Identification Medical equipment Pharmaceutical industry Medical device Adverse event Postmarketing surveillance Patient safety Medicine Health Clinical research
272	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 12:11:40 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
273	Definition and Glossary of Terms Used in GHTF Documents GHTF Steering Committee Final Document GHTF/SC/N4:2012 (Edition 2) GHTF/SC/N4:2012 (Edition 2) Add to Reading List Source URL: www.imdrf.org Language: English - Date: 2012-11-14 00:35:14 Pharmaceutical industry Health Clinical research Medical technology Food and Drug Administration Global Harmonization Task Force Medical device Unique Device Identification Clinical trial Medicine Technology Medical equipment
274	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 12:10:24 Health Medical device Center for Devices and Radiological Health Premarket approval Dexcom Federal Food Drug and Cosmetic Act Title 21 of the Code of Federal Regulations Adverse event Unique Device Identification Medicine Food and Drug Administration Technology
275	P080027 OraQuick Rapid HCV Antibody Test Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-05 19:51:26 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 HIV test Unique Device Identification Food and Drug Administration Medicine Health
276	P080029 Quick-Close® Vascular Suturing System Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:12:15 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 Investigational Device Exemption Unique Device Identification Food and Drug Administration Medicine Health
277	P090022 Softec HD Posterior Chamber hntraocular Lens (PCIOL) Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:11:58 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 Clinical research Adverse event Unique Device Identification Food and Drug Administration Medicine Health
278	P090003 Express® LD Iliac Premounted Stent System Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:12:06 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
279	P090006 Complete® SE Vascular Stent System (20-100mm lengths) Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:12:05 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
280	P980018/S010 HercepTestTM Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2013-12-06 12:10:14 Health Premarket approval Medical device Center for Devices and Radiological Health 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

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