Biermar AG
Country not established
- Devices
- 1
What Biermar AG makes
Biermar AG manufactures nebulizer devices, including the PUP II and Mini-Nebulizer, designed for delivering aerosolized medication to patients via inhalation.
These devices are regulated under the FDA’s 510(k) pathway and are listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Model Pup Ii And Mini-Nebulizer Ref K827291
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biermar AG have in the registry?
The registry currently lists 1 device for Biermar AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biermar AG's devices?
Among its 1 most recently registered device, Biermar AG has devices listed in FDA 510(k) (1 device).
What are the newest devices from Biermar AG in the registry?
The most recently registered devices listed for Biermar AG include MODEL PUP II AND MINI-NEBULIZER.