BEACMED S.R.L.

BEACMED S.R.L. specializes in electrostimulation devices designed for pelvic floor rehabilitation. Their product range includes vaginal and anal probes (such as the PERIPROBE series) for therapeutic applications, standalone stimulators like the IntelliSTIM BE-28E and evoStim variants, as well as specialized probes for men (e.g., KEAT Men Probe) and accessories like the Kegel8 Glide Gold Vaginal Probe. These devices are intended to support muscle stimulation and recovery in pelvic floor therapy.

BEACMED S.R.L. is based in Italy. The company’s headquarters and manufacturing operations are located within the country, adhering to regional regulatory and quality standards.

BEACMED S.R.L.’s devices are listed in the EUDAMED database, which is the European Union’s central registry for medical devices. This registry ensures transparency and traceability of devices authorized for use within the EU market.

All of BEACMED S.R.L.’s devices fall under Class IIa classification in the EU. This classification is assigned based on risk assessment criteria outlined in EU Medical Device Regulations (MDR) or the previous Medical Device Directive (MDD), indicating moderate risk and requiring compliance with specific design controls, clinical evaluations, and post-market surveillance.