Comercializadora Brever
MexicoFDA applicant, unverified
- Devices
- 1
What Comercializadora Brever makes
Comercializadora Brever manufactures sterilization wraps in two gram weights (70 gsm and 44 gsm) for use in hospital sterilization processes. These wraps are designed to protect medical instruments and equipment during autoclave sterilization.
The company’s sterilization wraps are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The products are based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Comercializadora Brever have in the registry?
The registry currently lists 1 device for Comercializadora Brever. Devices recorded under merged duplicate company entries are counted once.
Which registries list Comercializadora Brever's devices?
Among its 1 most recently registered device, Comercializadora Brever has devices listed in FDA 510(k) (1 device).
What risk classes do Comercializadora Brever's devices fall under?
Among its 1 most recently registered device, the classes recorded for Comercializadora Brever's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Comercializadora Brever in the registry?
The most recently registered devices listed for Comercializadora Brever include CDB Hospital ® Sterilization Wrap (70 gsm); CDB Hospital ® Sterilization Wrap (44 gsm).