Bristol-Myers Squibb
Country not established
- Devices
- 1
What Bristol-Myers Squibb makes
The company manufactures sterile, single-use bedside drainage bags, such as the PROSYS Model 650167, designed for collecting fluids from medical drainage systems.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Bristol-Myers Squibb have in the registry?
The registry currently lists 1 device for Bristol-Myers Squibb. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bristol-Myers Squibb's devices?
Among its 1 most recently registered device, Bristol-Myers Squibb has devices listed in FDA 510(k) (1 device).
What risk classes do Bristol-Myers Squibb's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bristol-Myers Squibb's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bristol-Myers Squibb in the registry?
The most recently registered devices listed for Bristol-Myers Squibb include PROSYS BEDSIDE DRAINAGE BAG (STERILE) MODEL 650167.