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Accession Number
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AVA19844-VNB1
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Title
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Medical Device Reporting (MDR) Forms for Device Manufacturers - How to Complete Form 3500A, Form 3417 and Form 3381 (VHS 1/2 inch) (Video).
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Publication Date
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1996
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Media Count
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1VHS video
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Personal Author
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N/A
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Abstract
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The Medical Device Reporting (MDR) Regulation requires the use of three forms for medical device manufacturers in reporting to FDA under the regulation. These forms include Form 3500A, Form 3417 Baseline Report, and Form 3381 Annual Certification. This vi ...
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Keywords
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Form 3381 Annual Certification
Form 3417 Baseline Report
Form 3500A
Forms
Instructions
Medical Device Reporting(MDR)
Regulations
Video tapes
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Source Agency
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Office of Communication Media Center for Devices and Radiological Health - FDA - Audiovisual
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NTIS Subject Category
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95C - Biomedical Instrumentation & Bioengineering
44H - Health Care Technology
44T - Data & Information Systems
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Corporate Author
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Food and Drug Administration, Rockville, MD. Center for Devices and Radiological Health.
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Document Type
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Audiovisual
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Title Note
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Audiovisual.
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NTIS Issue Number
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9619
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Contract Number
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N/A
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