Blease USA, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Blease USA, Inc. makes
Blease USA, Inc. manufactures the BLEAS ESIRIUC Anaesthesia System, offered in models 3000 and 2000, as well as a device named DATUM.
All of its products are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Datum Ref K942799
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Blease USA, Inc. have in the registry?
The registry currently lists 2 devices for Blease USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Blease USA, Inc.'s devices?
Among its 2 most recently registered devices, Blease USA, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Blease USA, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Blease USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Blease USA, Inc. in the registry?
The most recently registered devices listed for Blease USA, Inc. include BLEAS ESIRIUC ANAESTHSIA SYSTEM, MODELS 3000, 2000 and DATUM.