EQS-News: Viromed Medical AG
/ Key word(s): Agreement/Alliance
Viromed Medical AG reaches milestone for cooperation with multinational corporation The special approval by the Federal Institute for Drugs and Medical Devices (BfArM) for the medical device PulmoPlas® for the treatment of ventilator-associated pneumonia (VAP) based on an ongoing study led by Prof. Hortense Slevogt, Hannover Medical School, is expected to be applied for from Q3 2025. The phase 3 study is expected to be completed in Q2 2025. The classification process for ViroCAP® as a class 2a medical device is proceeding according to plan. In addition, series production of the ViroCAP® system has begun with the manufacture of injection molds. In the first stage, Viromed will have around 1,000 devices produced for use as medical devices in dermatology and veterinary medicine. Viromed Medical AG specializes in the development, manufacture and distribution of medical products. The operating business of the company, which has been listed on the stock exchange since October 2022, focuses on the distribution of innovative cold plasma technology for medical applications via its wholly owned subsidiary Viromed Medical GmbH. Viromed can draw on a broad customer base in the DACH region. Viromed Medical AG is pursuing the goal of further advancing the use of CAP in medicine in the coming years and realizing the corresponding growth potential. Uwe Perbandt
28.02.2025 CET/CEST Dissemination of a Corporate News, transmitted by EQS News - a service of EQS Group. |
Language: | English |
Company: | Viromed Medical AG |
Flensburger Straße 18 | |
25421 Pinneberg | |
Germany | |
Phone: | +49 4101 809960 |
E-mail: | kontakt@viromed-medical.de |
Internet: | https://www.viromed-medical-ag.de/ |
ISIN: | DE000A3MQR65 |
WKN: | A3MQR6 |
Listed: | Regulated Unofficial Market in Berlin, Dusseldorf (Primärmarkt), Frankfurt (Basic Board), Hamburg |
EQS News ID: | 2093535 |
End of News | EQS News Service |
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2093535 28.02.2025 CET/CEST
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