Roussel (Canada), Ltd.
Country not established
- Devices
- 1
What Roussel (Canada), Ltd. makes
Roussel (Canada), Ltd. manufactures the Clinifeeding System 1, a Class II medical device designed for enteral nutrition support in clinical settings.
The Clinifeeding System 1 is regulated under the FDA’s 510(k) pathway as a Class II device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Clinifeeding System 1 Ref K791758
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Roussel (Canada), Ltd. have in the registry?
The registry currently lists 1 device for Roussel (Canada), Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Roussel (Canada), Ltd.'s devices?
Among its 1 most recently registered device, Roussel (Canada), Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Roussel (Canada), Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Roussel (Canada), Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Roussel (Canada), Ltd. in the registry?
The most recently registered devices listed for Roussel (Canada), Ltd. include CLINIFEEDING SYSTEM 1.