Bremed Italia, S.r.l.
Country not established
- Devices
- 3
What Bremed Italia, S.r.l. makes
Bremed Italia, S.R.L. manufactures portable nebulizer devices, including the MASTER NEB II, ULTRANEB, and BRENEB, designed for delivering inhaled medications to patients.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Master Neb Ii Ref K970542
Regimes: 510(k) Registry: 510(k)Ultraneb Ref K974379
Regimes: 510(k) Registry: 510(k)Breneb Ref K982043
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bremed Italia, S.R.L. have in the registry?
The registry currently lists 3 devices for Bremed Italia, S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bremed Italia, S.R.L.'s devices?
Among its 3 most recently registered devices, Bremed Italia, S.R.L. has devices listed in FDA 510(k) (3 devices).
What risk classes do Bremed Italia, S.R.L.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Bremed Italia, S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bremed Italia, S.R.L. in the registry?
The most recently registered devices listed for Bremed Italia, S.R.L. include MASTER NEB II, ULTRANEB and BRENEB.