Eidosmed, LLC
Country not established
- Devices
- 1
What Eidosmed, LLC makes
Eidosmed, LLC manufactures the EDG4.0, a medical device designed for endoscopic ultrasound-guided fine-needle aspiration procedures, enabling tissue sampling and fluid collection during diagnostic imaging.
The EDG4.0 is classified as a Class II device under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Eidosmed, Model EDG4.0 Ref K091992
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eidosmed, LLC have in the registry?
The registry currently lists 1 device for Eidosmed, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eidosmed, LLC's devices?
Among its 1 most recently registered device, Eidosmed, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Eidosmed, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Eidosmed, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eidosmed, LLC in the registry?
The most recently registered devices listed for Eidosmed, LLC include EIDOSMED, MODEL EDG4.0.