BEACMED S.R.L.
IT-MF-000023616 · Italy · Portalbera (PV)
BEACMED S.R.L. is registered in the European database on medical devices as a manufacturer, with 71 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 71 |
|---|
Among these devices, 21 are declared active.
Devices declared under this manufacturer
- PERIPROBE AIR STIM
- PERIPROBE ANA-BF
- PERIPROBE ANALIA
- PERIPROBE Aerolys Vaginale
- PERIPROBE PERISIZE 4
- PERIPROBE VAG-2STF
- PERIPROBE VAG-2STW
- PERIPROBE VAG-BFT
- PERISPHERA L
- PERISPHERA Q
- PERISPHERA U
- evoStim E
Showing 12 of 71 declared devices.
Catalogue references include ANALIA, Aerolys Vaginale, Perisize 4, RU/ABF-n, evoStimE-001, evoStimE-002.
European nomenclature codes declared: U070399, Z120601,Z12062701, Z120601,Z12062499,Z12062701, Z12062701, Z120601, Z120622.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 71 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 71 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. BEACMED S.R.L. was not found in either the U.S. or the Canadian register.