Minos Medical
Country not established
- Devices
- 1
What Minos Medical makes
Minos Medical manufactures the MEGACHANNEL ENDOSCOPIC OVERTUBE (Model OT22), a reusable device designed for endoscopic procedures to facilitate instrument passage and improve procedural efficiency.
The MEGACHANNEL ENDOSCOPIC OVERTUBE (Model OT22) is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Megachannel Endoscopic Overtube, Model OT22 Ref K080550
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Minos Medical have in the registry?
The registry currently lists 1 device for Minos Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Minos Medical's devices?
Among its 1 most recently registered device, Minos Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Minos Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Minos Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Minos Medical in the registry?
The most recently registered devices listed for Minos Medical include MEGACHANNEL ENDOSCOPIC OVERTUBE, MODEL OT22.