Jostra Medizintechnik AG
Country not established
- Devices
- 2
What Jostra Medizintechnik AG makes
Jostra Medizintechnik AG manufactures a centrifugal pump system for extracorporeal circulation and a heparin-bonded arterial filter designed to remove emboli during cardiac procedures.
The company’s products are classified as Class II devices under FDA regulations and are listed in the 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Quart Arterial Filter, Model Hbf 140 Ref K001787
510(k) 510(k)Rotaflow Centrifugal Pump System Ref K991864
510(k) 510(k)
Frequently asked questions
How many devices does Jostra Medizintechnik AG have in the registry?
The registry currently lists 2 devices for Jostra Medizintechnik AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jostra Medizintechnik AG's devices?
Among its 2 most recently registered devices, Jostra Medizintechnik AG has devices listed in FDA 510(k) (2 devices).
What risk classes do Jostra Medizintechnik AG's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Jostra Medizintechnik AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Jostra Medizintechnik AG in the registry?
The most recently registered devices listed for Jostra Medizintechnik AG include QUART ARTERIAL FILTER, MODEL HBF 140 and ROTAFLOW CENTRIFUGAL PUMP SYSTEM.