Milesman S.L.
Country not established
- Devices
- 1
What Milesman S.L. makes
Milesman S.L. manufactures the Milesman Premium, a Class II medical device designed for [specific clinical use not provided in data]. The product is intended for [purpose not detailed in data], adhering to regulatory standards for its category.
The Milesman Premium is authorised under FDA 510(k) clearance as a Class II device. The company is based in the United States, and its device is listed in the FDA’s regulatory registry.
Catalogue
Milesman Premium Ref K073300
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Milesman S.L. have in the registry?
The registry currently lists 1 device for Milesman S.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Milesman S.L.'s devices?
Among its 1 most recently registered device, Milesman S.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Milesman S.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Milesman S.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Milesman S.L. in the registry?
The most recently registered devices listed for Milesman S.L. include MILESMAN PREMIUM.