Stoeckert Instrumente
Country not established
- Devices
- 13
What Stoeckert Instrumente makes
Stoeckert Instrumente manufactures perfusion equipment and accessories, including the Stockert Compact System, S3 pump modules, and various control units for cardioplegia, RPM, and power supply. Their product portfolio also features specialized surgical components such as pediatric aortic cannulae, arterial femoral cannulae, and cardiac pacing electrodes.
The company is based in the US, and its devices are categorized under Class I, Class II, and Class III regulatory classifications. These products are listed in the FDA 510(k) registry.
Catalogue
Search and filter all 13 devicesFrequently asked questions
How many devices does Stoeckert Instrumente have in the registry?
The registry currently lists 13 devices for Stoeckert Instrumente. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stoeckert Instrumente's devices?
Among its 13 most recently registered devices, Stoeckert Instrumente has devices listed in FDA 510(k) (13 devices).
What risk classes do Stoeckert Instrumente's devices fall under?
Among its 13 most recently registered devices, the classes recorded for Stoeckert Instrumente's devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Stoeckert Instrumente in the registry?
The most recently registered devices listed for Stoeckert Instrumente include STOCKERT COMPACT SYSTEM VERSION 2.0, INTERFACE MODULE IDDD, STOCKERT S3 DOUBLE HEAD PUMP MODULE and S3 CYCLIC RPM CONTROL.