R. Bell
Country not established
- Devices
- 1
What R. Bell makes
R. Bell manufactures sample manifold holders, which are designed to support and stabilize laboratory apparatus used in fluid handling and sample preparation processes. These devices are commonly employed in clinical, research, and industrial settings to ensure precise and consistent sample processing.
The company’s sample manifold holders are classified as Class II medical devices under FDA regulations and are listed via the 510(k) clearance pathway. These products are intended for use in the United States, where they must comply with applicable FDA requirements for safety and performance.
Catalogue
Sample Manifold Holder Ref K860889
510(k) 510(k)
Frequently asked questions
How many devices does R. Bell have in the registry?
The registry currently lists 1 device for R. Bell. Devices recorded under merged duplicate company entries are counted once.
Which registries list R. Bell's devices?
Among its 1 most recently registered device, R. Bell has devices listed in FDA 510(k) (1 device).
What risk classes do R. Bell's devices fall under?
Among its 1 most recently registered device, the classes recorded for R. Bell's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from R. Bell in the registry?
The most recently registered devices listed for R. Bell include SAMPLE MANIFOLD HOLDER.