GE Medical Systems F.I. Haifa
IsraelFDA applicant, unverified
- Devices
- 17
What GE Medical Systems F.I. Haifa makes
The company manufactures nuclear medicine imaging systems, including the Quasar nuclear medicine system and the Discovery NM/CT 670, which combine nuclear and computed tomography imaging. It also produces processing and review workstations like the Xeleris 3 and Xeleris 3.1, as well as software applications for processing nuclear imaging data, such as QPS/BPGS/MOCO for the Entegra workstation. Additional offerings include attenuation correction systems (MG ATC and VTransact) for dual-head gamma cameras, photon energy recovery options, and the MyoLight system for specialized imaging. Ventri and Ventri 1.1 are part of its nuclear medicine workflow solutions.
These devices are classified under Class II in the US and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Search and filter all 17 devicesFrequently asked questions
How many devices does Ge Medical Systems F.I. Haifa have in the registry?
The registry currently lists 17 devices for Ge Medical Systems F.I. Haifa. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ge Medical Systems F.I. Haifa's devices?
Among its 17 most recently registered devices, Ge Medical Systems F.I. Haifa has devices listed in FDA 510(k) (17 devices).
What risk classes do Ge Medical Systems F.I. Haifa's devices fall under?
Among its 17 most recently registered devices, the classes recorded for Ge Medical Systems F.I. Haifa's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ge Medical Systems F.I. Haifa in the registry?
The most recently registered devices listed for Ge Medical Systems F.I. Haifa include QPS/BPGS/MOCO PROCESSING APPLICATIONS FOR ENTEGRA WORKSTATION, VENTRI 1.1, XELERIS 3 PROCESSING AND REVIEW WORKSTATION and GE PHOTON ENERGY RECOVERY (PER) OPTION.