Medical Enterprises, Ltd.
Country not established
- Devices
- 1
What Medical Enterprises, Ltd. makes
Medical Enterprises, Ltd. manufactures the UNILYTE A, a medical device designed for [specific clinical purpose implied by the name, e.g., urinary catheterization or drainage], as indicated by its classification and regulatory pathway.
The UNILYTE A is classified as a Class II device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Unilyte A Ref K843623
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Enterprises, Ltd. have in the registry?
The registry currently lists 1 device for Medical Enterprises, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Enterprises, Ltd.'s devices?
Among its 1 most recently registered device, Medical Enterprises, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Medical Enterprises, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medical Enterprises, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Enterprises, Ltd. in the registry?
The most recently registered devices listed for Medical Enterprises, Ltd. include UNILYTE A.