Provision 5706/2017
Information
Type
Regulation
Regulated products
Medical Devices
Topics
General Standards For Medical Products, Registration Of Medical Products
Published
January 1, 2017
Last updated
January 1, 2017
Description
This provision shall apply to applications for registration, modification and revalidation of Class I and II medical products and applications for modification of some characteristic data of Class III and IV medical products authorized by this Administration. B.O. June 2, 2017.
Tags
Organization
Country / Region
Argentina
License
Creative Commons Attribution 4.0