Lauer Membran Wassertechnik GmbH
GermanyFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lauer Membran Wassertechnik GmbH have in the registry?
The registry currently lists 1 device for Lauer Membran Wassertechnik GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lauer Membran Wassertechnik GmbH's devices?
Among its 1 most recently registered device, Lauer Membran Wassertechnik GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Lauer Membran Wassertechnik GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lauer Membran Wassertechnik GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lauer Membran Wassertechnik GmbH in the registry?
The most recently registered devices listed for Lauer Membran Wassertechnik GmbH include AQUABOSS ECORO DIA I (HT); AQUABOSS ECORO DIA II (HT).