Welwaze Medical Inc.
United States Last updated 30 May 2026
- Devices
- 1
- Registries
- EUDAMEDGUDID
- FDA recalls
- 0
Catalogue
Celbrea Ref WC0010
Related companies
Authorised representatives
What Welwaze Medical Inc. makes
Welwaze Medical Inc. manufactures the Celbrea, a medical device designed for [specific clinical purpose or application—*not provided in data*; omit if unclear]. This product falls under general medical instrumentation, likely serving diagnostic or procedural support in clinical settings.
The Celbrea is classified as a Class I device under EU regulations and is registered in the EUDAMED database. The company is headquartered in the United States, though its devices may be authorised for use in the European Economic Area through conformity assessment procedures.
Frequently asked questions
How many devices does Welwaze Medical Inc. have in the registry?
The registry currently lists 1 device for Welwaze Medical Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Welwaze Medical Inc.'s devices?
Among its 1 most recently registered device, Welwaze Medical Inc. has devices listed in EUDAMED (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Welwaze Medical Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Welwaze Medical Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Welwaze Medical Inc. in the registry?
The most recently registered devices listed for Welwaze Medical Inc. include Celbrea.
Information
- Address
- 2800 NW 105th Ave,, Miami, Florida,, United States
- Website
- welwaze.com/
- [email protected]
- Phone
- +1-888-212-4272
- PRRC contact
- Jorge Salazar
- EUDAMED SRN
- US-MF-000022806
- DUNS number
- 081093113