Extension of the MDD Certificate for Our Medical Devices Supporting Women’s Wellness at Every Stage of Life The MDR Regulation, in effect since May 2017 and applicable from May 2021, governs medical devices in Europe. Deadline extensions allow the marketing of devices compliant with the Medical Device Directive (MDD) until December 31, 2027, for class…
Ear Spray for Hygiene: Cerumen Removal and Prevention of Irritation and Inflammation – Class I Medical Device We recently registered in Jordan for a Class I medical device: an ear spray with a gas-free cannula, formulated with sodium chloride (NaCl) and boric acid. This product is specifically indicated for the hygiene of the ear cavities,…
Treatment for Vulvovaginal Mycotic Infections: FarmaImpresa Group certifies a new Medical Device in Macedonia We have completed the registration with the competent authorities in Macedonia for a Class I medical device, designed for the treatment of vulvovaginal mycotic infections. The medical device is formulated as a vaginal suppository based on hyaluronic acid, boric acid, and…