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.

Organization

Country / Region

Argentina

License

Creative Commons Attribution 4.0

Feedback

Suggest an improvement to this page

Actions

Social networks

Embed