Ferno Ille
Country not established
- Devices
- 1
What Ferno Ille makes
Ferno Ille manufactures the HYDROTRACK, a device designed for patient transfer and repositioning in clinical settings, including hospitals and emergency medical services. This product is intended to assist healthcare providers in safely moving patients with minimal risk of injury or discomfort, particularly in scenarios requiring hydration or fluid management during transport.
The HYDROTRACK is classified as a Class I medical device under FDA regulations and has been submitted for clearance via the 510(k) pathway. The company is based in the United States, where its devices are subject to compliance with U.S. regulatory requirements.
Catalogue
Hydrotrack Ref K935509
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ferno Ille have in the registry?
The registry currently lists 1 device for Ferno Ille. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ferno Ille's devices?
Among its 1 most recently registered device, Ferno Ille has devices listed in FDA 510(k) (1 device).
What risk classes do Ferno Ille's devices fall under?
Among its 1 most recently registered device, the classes recorded for Ferno Ille's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ferno Ille in the registry?
The most recently registered devices listed for Ferno Ille include HYDROTRACK.