Xeridiem (Formerly MRI)
Country not established
- Devices
- 2
What Xeridiem (Formerly MRI) makes
Xeridiem manufactures balloon dilation kits and extension sets for endoscopic procedures, including low-profile balloon systems and medication delivery extensions. It also produces multi-lumen gastrostomy feeding tubes designed for nutritional support, available in bi-funnel and tri-funnel configurations.
The company’s products are classified as Class II medical devices under FDA regulations and are authorised via the 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Xeridiem (Formerly Mri) have in the registry?
The registry currently lists 2 devices for Xeridiem (Formerly Mri). Devices recorded under merged duplicate company entries are counted once.
Which registries list Xeridiem (Formerly Mri)'s devices?
Among its 2 most recently registered devices, Xeridiem (Formerly Mri) has devices listed in FDA 510(k) (2 devices).
What risk classes do Xeridiem (Formerly Mri)'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Xeridiem (Formerly Mri)'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Xeridiem (Formerly Mri) in the registry?
The most recently registered devices listed for Xeridiem (Formerly Mri) include Endo Vive 3S Low Profile Balloon Kit, Endo Vive 3S Bolus Extension Sets, Endo Vive 3S Continuous Extension Sets, Endo Vive 3S Medication Extension Set and BI-FUNNEL GASTROSTOMY FEEDING TUBE, TRI-FUNNEL GASTROSTOMY FEEDING TUBE.