Bremi
NetherlandsFDA 510(k) applicant, unverified
- Devices
- 1
What Bremi makes
Bremi manufactures UVA sun systems designed for therapeutic or cosmetic skin treatments, utilizing controlled ultraviolet A light exposure.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Uva Sun Systems Ref K860859
510(k) 510(k)
Frequently asked questions
How many devices does Bremi have in the registry?
The registry currently lists 1 device for Bremi. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bremi's devices?
Among its 1 most recently registered device, Bremi has devices listed in FDA 510(k) (1 device).
What risk classes do Bremi's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bremi's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bremi in the registry?
The most recently registered devices listed for Bremi include UVA SUN SYSTEMS.