According to D.R. No. 033-2017-DIGEMID-DG-MINSA, published early this year, DIGEMID issued a list of medical devices that may be marketed directly to end-users. This document does not list every medical device but establishes a criterion based on MD risk classification. Medical Devices Class I, II, III, and IV Laboratories and droguerías (pharmaceutical establishments) may directly
Pharma Consulting warns the general public about the danger of acquiring pharmaceutical products, medical devices, and other health products in unauthorized establishments or through advertisements on social networks and e-commerce websites. We express our concern about an increase in advertisements for products that lack the registration required, advertisements that proclaim unauthorized benefits, or therapeutic properties