Schneider (Europe) GmbH
Country not established
- Devices
- 5
What Schneider (Europe) GmbH makes
Schneider (Europe) GmbH manufactures coronary guidewires, including the Docking-Extension Wire, Clyde, Hannibal, and C-Thru, designed for use in percutaneous coronary interventions. The company also produces the Flamingo Wallstent Esophageal Endoprosthesis, a stent for esophageal strictures or leaks.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Docking-Extension Wire Ref K982592
Regimes: 510(k) Registry: 510(k)Clyde Coronary Guidewire Ref K970528
Regimes: 510(k) Registry: 510(k)Hannibal Guidewire Ref K970494
Regimes: 510(k) Registry: 510(k)C-Thru Coronary Guide Wire Ref K951109
Regimes: 510(k) Registry: 510(k)Flamingo Wallstent Esophageal Endoprosthesis Ref K984068
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Schneider (Europe) GmbH have in the registry?
The registry currently lists 5 devices for Schneider (Europe) GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Schneider (Europe) GmbH's devices?
Among its 5 most recently registered devices, Schneider (Europe) GmbH has devices listed in FDA 510(k) (5 devices).
What risk classes do Schneider (Europe) GmbH's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Schneider (Europe) GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Schneider (Europe) GmbH in the registry?
The most recently registered devices listed for Schneider (Europe) GmbH include DOCKING-EXTENSION WIRE, CLYDE CORONARY GUIDEWIRE, HANNIBAL GUIDEWIRE and C-THRU CORONARY GUIDE WIRE.