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Unique Device Identification System (US Food and Drug Administration Regulation) (FDA) (2018 Edition) - Softcover
Synopsis
Unique Device Identification System (US Food and Drug Administration Regulation) (FDA) (2018 Edition) The Law Library presents the complete text of the Unique Device Identification System (US Food and Drug Administration Regulation) (FDA) (2018 Edition). Updated as of May 29, 2018 The Food and Drug Administration (FDA) is issuing a final rule to establish a system to adequately identify devices through distribution and use. This rule requires the label of medical devices to include a unique device identifier (UDI), except where the rule provides for an exception or alternative placement. The labeler must submit product information concerning devices to FDA's Global Unique Device Identification Database (GUDID), unless subject to an exception or alternative. The system established by this rule requires the label and device package of each medical device to include a UDI and requires that each UDI be provided in a plain-text version and in a form that uses automatic identification and data capture (AIDC) technology. The UDI will be required to be directly marked on the device itself if the device is intended to be used more than once and intended to be reprocessed before each use. This book contains: - The complete text of the Unique Device Identification System (US Food and Drug Administration Regulation) (FDA) (2018 Edition) - A table of contents with the page number of each section
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Unique Device Identification System (US Food and Drug Administration Regulation) (FDA) (2018 Edition)
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CreateSpace Independent Publishing Platform, 2018
ISBN 10: 1727701925
ISBN 13: 9781727701920
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Softcover
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Unique Device Identification System (US Food and Drug Administration Regulation) (FDA) (2018 Edition)
Published by
CreateSpace Independent Publishing Platform, 2018
ISBN 10: 1727701925
ISBN 13: 9781727701920
New
Softcover
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Unique Device Identification System (US Food and Drug Administration Regulation) (FDA) (2018 Edition)
Published by
Createspace Independent Publishing Platform, 2018
ISBN 10: 1727701925
ISBN 13: 9781727701920
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Paperback / softback
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Unique Device Identification System (US Food and Drug Administration Regulation) (FDA) (2018 Edition)
Published by
CreateSpace Independent Publishing Platform, 2018
ISBN 10: 1727701925
ISBN 13: 9781727701920
Used
Softcover
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Condition: very good. Gut/Very good: Buch bzw. Schutzumschlag mit wenigen Gebrauchsspuren an Einband, Schutzumschlag oder Seiten. / Describes a book or dust jacket that does show some signs of wear on either the binding, dust jacket or pages. Seller Inventory # M01727701925-V
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Unique Device Identification System (US Food and Drug Administration Regulation) (FDA) (2018 Edition) (Paperback)
Published by
Createspace Independent Publishing Platform, 2018
ISBN 10: 1727701925
ISBN 13: 9781727701920
New
Paperback
Seller: CitiRetail, Stevenage, United Kingdom
Seller rating 5 out of 5 stars
Paperback. Condition: new. Paperback. Unique Device Identification System (US Food and Drug Administration Regulation) (FDA) (2018 Edition) The Law Library presents the complete text of the Unique Device Identification System (US Food and Drug Administration Regulation) (FDA) (2018 Edition). Updated as of May 29, 2018 The Food and Drug Administration (FDA) is issuing a final rule to establish a system to adequately identify devices through distribution and use. This rule requires the label of medical devices to include a unique device identifier (UDI), except where the rule provides for an exception or alternative placement. The labeler must submit product information concerning devices to FDA's Global Unique Device Identification Database (GUDID), unless subject to an exception or alternative. The system established by this rule requires the label and device package of each medical device to include a UDI and requires that each UDI be provided in a plain-text version and in a form that uses automatic identification and data capture (AIDC) technology. The UDI will be required to be directly marked on the device itself if the device is intended to be used more than once and intended to be reprocessed before each use. This book contains: - The complete text of the Unique Device Identification System (US Food and Drug Administration Regulation) (FDA) (2018 Edition) - A table of contents with the page number of each section Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability. Seller Inventory # 9781727701920
Quantity: 1 available