Nu-Rise, SA
PortugalFDA applicant, unverified
- Devices
- 1
What Nu-Rise, SA makes
Nu-Rise, SA manufactures the PRO-DOSE System, a medical device designed for precise dosing and delivery of pharmaceuticals in clinical or procedural settings. This system is intended to automate medication administration, ensuring accurate and controlled delivery to patients.
The PRO-DOSE System is classified as a Class II device under FDA regulations and has undergone the 510(k) clearance process. The company is based in the United States, and the device is listed in the FDA’s 510(k) registry.
Catalogue
PRO-DOSE System Ref K250083
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nu-Rise, SA have in the registry?
The registry currently lists 1 device for Nu-Rise, SA. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nu-Rise, SA's devices?
Among its 1 most recently registered device, Nu-Rise, SA has devices listed in FDA 510(k) (1 device).
What risk classes do Nu-Rise, SA's devices fall under?
Among its 1 most recently registered device, the classes recorded for Nu-Rise, SA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nu-Rise, SA in the registry?
The most recently registered devices listed for Nu-Rise, SA include PRO-DOSE System.