Bayer U.S., LLC
Country not established
- Devices
- 1
What Bayer U.S., LLC makes
Bayer U.S., LLC manufactures the MEDRAD® Imaging Bulk Package Transfer Set, a sterile, single-use device designed for transferring contrast media in medical imaging procedures.
This product is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
MEDRAD® Imaging Bulk Package Transfer Set Ref K173913
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bayer U.S., LLC have in the registry?
The registry currently lists 1 device for Bayer U.S., LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bayer U.S., LLC's devices?
Among its 1 most recently registered device, Bayer U.S., LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Bayer U.S., LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bayer U.S., LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bayer U.S., LLC in the registry?
The most recently registered devices listed for Bayer U.S., LLC include MEDRAD® Imaging Bulk Package Transfer Set.