|
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
|
|
|
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
|
