Biobarrier, Inc.
Country not established
- Devices
- 1
What Biobarrier, Inc. makes
Biobarrier, Inc. manufactures The Double Glove, a sterile barrier device designed to reduce contamination risk during medical procedures by providing an additional layer of protection between healthcare providers and patients.
The company’s portfolio is regulated under FDA Class I devices and includes products listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
The Double Glove Ref K060030
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biobarrier, Inc. have in the registry?
The registry currently lists 1 device for Biobarrier, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biobarrier, Inc.'s devices?
Among its 1 most recently registered device, Biobarrier, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Biobarrier, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Biobarrier, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Biobarrier, Inc. in the registry?
The most recently registered devices listed for Biobarrier, Inc. include THE DOUBLE GLOVE.