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Accession Number AVA12486-VM00
Title Medical Device Reporting Regulation.
Publication Date 1994
Media Count 1AV-Beta 2 - 1 cassette
Personal Author N/A
Abstract This program provides an overview of the regulation which requires manufacturers and importers of medical devices to report to FDA whenever they receive information suggesting that one of their devices may have caused or contributed to a death or serious ...
Keywords Deaths
Imports
Liability
Manufacturing
Medical devices
Medical equipment
Regulations
Reporting requirements
US FDA
Wounds and injuries
 
Please call 1-800-553-6847 or 703-605-6000 to order (NTIS Order Number AVA12486-VM00).
Source Agency Office of Communication Media Center for Devices and Radiological Health - FDA - Audiovisual
NTIS Subject Category 95A - Prosthetics & Mechanical Organs
95C - Biomedical Instrumentation & Bioengineering
44H - Health Care Technology
92D - Education, Law, & Humanities
Corporate Author Food and Drug Administration, Rockville, MD. Office of Communication Media Center for Devices and Radiological Health.
Document Type Audiovisual
Title Note N/A
NTIS Issue Number 0001
Contract Number N/A

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