Eris Medical Technology
Country not established
- Devices
- 3
What Eris Medical Technology makes
Eris Medical Technology produces diagnostic systems and accessories for urological procedures, including the ERIS URO-DIAGNOSTIC SYSTEM for imaging and analysis, a CATHETER WITHDRAWAL UNIT for safe catheter handling, and a FILLING VOLUME OPTION for procedural fluid management.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Eris Uro-Diagnostic System Ref K850169
Regimes: 510(k) Registry: 510(k)Catheter Withdrawal Unit Ref K881878
Regimes: 510(k) Registry: 510(k)Filling Volume Option Ref K882295
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eris Medical Technology have in the registry?
The registry currently lists 3 devices for Eris Medical Technology. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eris Medical Technology's devices?
Among its 3 most recently registered devices, Eris Medical Technology has devices listed in FDA 510(k) (3 devices).
What risk classes do Eris Medical Technology's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Eris Medical Technology's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eris Medical Technology in the registry?
The most recently registered devices listed for Eris Medical Technology include ERIS URO-DIAGNOSTIC SYSTEM, CATHETER WITHDRAWAL UNIT and FILLING VOLUME OPTION.