Loversan
Country not established
- Devices
- 3
What Loversan makes
Loversan manufactures sterile infusion and administration sets, including devices for delivering intravenous fluids, blood, and plasma. These products are designed for single-use medical procedures to ensure aseptic administration of therapeutic solutions.
The company’s portfolio is regulated under FDA’s Class II device classification, with products listed via the 510(k) pathway. These devices are registered in the FDA’s 510(k) database and comply with U.S. medical device regulations.
Catalogue
Infusion Set-Sterile Ref K840409
Regimes: 510(k) Registry: 510(k)Solution Admin. Set Sterile Ref K840410
Regimes: 510(k) Registry: 510(k)Blood & Plasma Admin. Dev-Sterile Ref K840411
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Loversan have in the registry?
The registry currently lists 3 devices for Loversan. Devices recorded under merged duplicate company entries are counted once.
Which registries list Loversan's devices?
Among its 3 most recently registered devices, Loversan has devices listed in FDA 510(k) (3 devices).
What risk classes do Loversan's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Loversan's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Loversan in the registry?
The most recently registered devices listed for Loversan include INFUSION SET-STERILE, SOLUTION ADMIN. SET STERILE and BLOOD & PLASMA ADMIN. DEV-STERILE.