Stimel, Ltd.
Country not established
- Devices
- 1
What Stimel, Ltd. makes
Stimel, Ltd. manufactures the STIMEL-03, a medical device designed for [specific application not detailed in provided data].
The device is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Stimel-03 Ref K130424
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stimel, Ltd. have in the registry?
The registry currently lists 1 device for Stimel, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stimel, Ltd.'s devices?
Among its 1 most recently registered device, Stimel, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Stimel, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Stimel, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stimel, Ltd. in the registry?
The most recently registered devices listed for Stimel, Ltd. include STIMEL-03.