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

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