Eureduc
FranceFDA 510(k) applicant, unverified
- Devices
- 2
What Eureduc makes
Eureduc manufactures pneumatic drainage systems, including the Model TP03, designed for medical applications requiring controlled fluid evacuation from body cavities or surgical sites.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The portfolio is regulated in the United States.
Catalogue
Eureduc Pneumatic Drainage System Model TP03 Ref K960902
510(k) 510(k)Eureduc Pneumatic Drainage System Ref K954788
510(k) 510(k)
Frequently asked questions
How many devices does Eureduc have in the registry?
The registry currently lists 2 devices for Eureduc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eureduc's devices?
Among its 2 most recently registered devices, Eureduc has devices listed in FDA 510(k) (2 devices).
What risk classes do Eureduc's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Eureduc's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eureduc in the registry?
The most recently registered devices listed for Eureduc include EUREDUC PNEUMATIC DRAINAGE SYSTEM MODEL TP03 and EUREDUC PNEUMATIC DRAINAGE SYSTEM.