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Unique Device Identification
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71	Federal Register / Vol. 79, No[removed]Friday, November 21, [removed]Notices Reduction Act of[removed]U.S.C. 3501– [removed]The collections of information in 21 CFR[removed]and Form FDA 356h have been approved under OMB con Add to Reading List Source URL: www.gpo.gov Language: English - Date: 2014-11-21 08:51:04 Pharmacology Unique Device Identification Dermatologic and Ophthalmic Drugs Advisory Committee Food and Drug Administration Pharmaceutical sciences Clinical research
72	Microsoft Word - finaldraft 010608clean _3_.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-03 12:43:06 Pharmacology Food and Drug Administration European Union directives Medical equipment Pharmaceutical industry Medical device Medical Devices Directive Unique Device Identification Global Harmonization Task Force Medicine Health Technology
73	Today the legislative framework for medical devices in Europe comprises three main Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-03 12:39:14 Medical technology Medical device European Union directives Pharmaceutical industry Medical Devices Directive CE mark Notified Body Unique Device Identification Breast implant Medicine Technology Medical equipment
74	MEDICAL INNOVATION When it comes to medical devices in the European Union, explains Commissioner Neven Mimica, the European Commission wishes to ensure patient safety while promoting innovation Add to Reading List Source URL: www.paneuropeannetworks.com Language: English - Date: 2014-08-20 10:45:12 Medical equipment Pharmacology Clinical research Pharmaceutical industry Medical device Patient safety Unique Device Identification Clinical trial Medicine Health Food and Drug Administration
75	Microsoft Word - Agenda_Denmark_draft_v40 Add to Reading List Source URL: www.gs1.org Language: English - Date: 2014-10-14 09:13:33 Medicine Standards organizations Technology Food and Drug Administration Unique Device Identification Automatic identification and data capture GS1 Global Data Synchronization Network Traceability Identification Identifiers Barcodes
76	EDMA R ESPONSE – EU C OMMISSION C ONSULT ATION D IRECTIVES ON THE R ECAS T M EDIC AL D EV ICE S Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-03 12:43:21 Medical technology Medical device Global Harmonization Task Force Medical Devices Directive CE mark Notified Body IVD Unique Device Identification Medicine Technology Medical equipment
77	EDMA R ESPONSE – EU C OMMISSION C ONSULT ATION D IRECTIVES ON THE R ECAS T M EDIC AL D EV ICE S Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-03 12:43:19 Medical technology Medical device Global Harmonization Task Force Medical Devices Directive CE mark Notified Body IVD Unique Device Identification Medicine Technology Medical equipment
78	Microsoft Word - Recast_NAM.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-03 12:39:14 Medical technology Global Harmonization Task Force Medical device CE mark Unique Device Identification Notified Body Medical equipment Medicine Technology
79	Microsoft Word[removed]UDI Ltr to Burwell Sept 23 w sig.docx Add to Reading List Source URL: www.ncvhs.hhs.gov Language: English - Date: 2014-10-02 20:39:26 Health Insurance Portability and Accountability Act Privacy law Electronic health record Patient safety Udi people Patient Protection and Affordable Care Act Unique Device Identification Medicine Health Data privacy
80	Agenda for Quarterly Meeting on MDUFA III (FY[removed]Performance November 18, [removed]:00 A.M. Welcome. Barbara Zimmerman, CDRH-ODE. Guidance Development • Add to Reading List Source URL: www.fda.gov Language: English Health Premarket approval Investigational Device Exemption Center for Devices and Radiological Health Medical device Humanitarian Device Exemption Unique Device Identification Food and Drug Administration Medicine Technology

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