Maxter Catheters
FranceFDA applicant, unverified
- Devices
- 1
What Maxter Catheters makes
Maxter Catheters specializes in enteral feeding tubes and associated accessories, including the MGX/YY model designed for nutritional support delivery.
Their portfolio is regulated under FDA Class II devices, with products listed via the 510(k) clearance pathway. The company operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Maxter Catheters have in the registry?
The registry currently lists 1 device for Maxter Catheters. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maxter Catheters's devices?
Among its 1 most recently registered device, Maxter Catheters has devices listed in FDA 510(k) (1 device).
What risk classes do Maxter Catheters's devices fall under?
Among its 1 most recently registered device, the classes recorded for Maxter Catheters's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maxter Catheters in the registry?
The most recently registered devices listed for Maxter Catheters include MEDICINA ENTERAL FEEDING TUBES AND ACCESSORIES MODEL MGX/YY.