Nilimedix, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Nilimedix, Ltd. makes
Nilimedix, Ltd. manufactures the NILIMEDIX ADI, a medical device designed for [specific application or function not provided in data]. This product is intended for [clinical use or purpose not detailed in data].
The NILIMEDIX ADI is classified under Class II devices and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Nilimedix Adi Ref K070844
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nilimedix, Ltd. have in the registry?
The registry currently lists 1 device for Nilimedix, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nilimedix, Ltd.'s devices?
Among its 1 most recently registered device, Nilimedix, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Nilimedix, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nilimedix, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nilimedix, Ltd. in the registry?
The most recently registered devices listed for Nilimedix, Ltd. include NILIMEDIX ADI.