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Unique Device Identification
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#	Item
311	Document number: GHTF/AHWG Title: Unique Device Identification (UDI) System Submitted by (name): GS1 Healthcare Comment Add to Reading List Source URL: www.gs1.org Language: English - Date: 2010-04-13 09:25:38 Information Barcodes Universal identifiers Automatic identification and data capture Technology Unique Device Identification Global Trade Item Number Radio-frequency identification GS1 Identification Identifiers Computing
312	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: 2013-12-24 12:27:32 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
313	Federal Register / Vol. 71, No[removed]Tuesday, July 25, [removed]Notices Notice of this meeting is given under the Federal Advisory Committee Act (5 U.S.C. app. 2). Dated: July 17, 2006. Randall W. Lutter, Add to Reading List Source URL: www.fda.gov Language: English - Date: 2006-07-25 08:01:14 Pharmacology Clinical pharmacology Therapeutics United States Public Health Service Federal Advisory Committee Act Unique Device Identification Food and Drug Administration Pharmaceutical sciences Clinical research
314	A Safer, Clearer, and Faster Course to Market Insights and Guidance for the Medical Technology Industry on the Role of Standards with Biocompatibility, Risk Management, and Sterility A Report on ... Add to Reading List Source URL: www.aami.org Language: English - Date: 2014-07-24 11:00:38 Medical device Medical equipment Medical technology ISO 10993 Center for Devices and Radiological Health Biocompatibility Association for the Advancement of Medical Instrumentation Unique Device Identification Medicine Health Food and Drug Administration
315	ycherry on PROD1PC64 with NOTICES[removed]Federal Register / Vol. 71, No[removed]Thursday, October 26, [removed]Notices Add to Reading List Source URL: www.fda.gov Language: English - Date: 2006-10-26 08:20:31 Pharmaceutical sciences MedWatch Premarket approval Center for Devices and Radiological Health Medical device Rosiglitazone Unique Device Identification Federal Food Drug and Cosmetic Act Food and Drug Administration Medicine Health
316	GS1 Healthcare Newsletter No. 17 – Winter[removed]Also in this issue: Add to Reading List Source URL: www.ismp-canada.org Language: English - Date: 2010-10-05 15:12:47 Universal identifiers Standards organizations Electronic commerce GS1 Unique Device Identification Global Data Synchronization Network Global Trade Item Number Global Location Number Traceability Identification Barcodes Identifiers
317	PDF Document Add to Reading List Source URL: docs.house.gov Language: English - Date: 2014-07-21 16:43:11 Technology Unique Device Identification Medical device Center for Devices and Radiological Health Premarket approval Adverse event Clinical research Food and Drug Administration Modernization Act Disease registry Food and Drug Administration Medicine Health
318	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: 2014-01-15 14:08:44 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
319	PDF Document Add to Reading List Source URL: www.fda.gov Language: English - Date: 2006-06-16 09:54:34 Pharmaceutical sciences Center for Devices and Radiological Health Medical device Unique Device Identification Food and Drug Administration Medicine Health
320	DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration General and Plastic Surgery Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting AGENCY: ACTION: Add to Reading List Source URL: www.fda.gov Language: English - Date: 2006-07-24 09:44:28 Technology Center for Devices and Radiological Health Medical device Premarket approval Federal Advisory Committee Act Unique Device Identification Food and Drug Administration Medicine Health

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