Angiologica B. M. SRL
ItalyFDA applicant, unverified
- Devices
- 2
What Angiologica B. M. SRL makes
Angiologica B. M. Srl manufactures vascular repair and occlusion devices, including the HEMORPEX SYSTEM for hemorrhoidal treatment and the REPOL line of endovascular occlusion products. These include mesh implants (REPOL ANGIMESH, FOLDED MESH), plug systems (REPOL PLUG BASIC, REPOL PLUG FLOWER AND WINGS MESH), and accessories like the REPOL PLUG CAP.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices. Products are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Hemorpex System Ref K090432
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Angiologica B. M. Srl have in the registry?
The registry currently lists 2 devices for Angiologica B. M. Srl. Devices recorded under merged duplicate company entries are counted once.
Which registries list Angiologica B. M. Srl's devices?
Among its 2 most recently registered devices, Angiologica B. M. Srl has devices listed in FDA 510(k) (2 devices).
What risk classes do Angiologica B. M. Srl's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Angiologica B. M. Srl's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Angiologica B. M. Srl in the registry?
The most recently registered devices listed for Angiologica B. M. Srl include HEMORPEX SYSTEM and REPOL ANGIMESH, ANGIMESH PRE, FOLDED MESH, REPOL PLUG BASIC, REPOL PLUG CAP, REPOL PLUG FLOWER AND WINGS MESH.