Noblitt & Rueland
Country not established
- Devices
- 1
What Noblitt & Rueland makes
Noblitt & Rueland manufactures the BM3 and BM3 PLUS, which are medical devices designed for blood monitoring or processing applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
BM3/BM3 Plus Ref K132033
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Noblitt & Rueland have in the registry?
The registry currently lists 1 device for Noblitt & Rueland. Devices recorded under merged duplicate company entries are counted once.
Which registries list Noblitt & Rueland's devices?
Among its 1 most recently registered device, Noblitt & Rueland has devices listed in FDA 510(k) (1 device).
What risk classes do Noblitt & Rueland's devices fall under?
Among its 1 most recently registered device, the classes recorded for Noblitt & Rueland's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Noblitt & Rueland in the registry?
The most recently registered devices listed for Noblitt & Rueland include BM3/BM3 PLUS.