Siemens Molecular Imaging, Ltd.
Country not established
- Devices
- 2
What Siemens Molecular Imaging, Ltd. makes
Siemens Molecular Imaging, Ltd. makes nuclear medicine imaging devices, specifically the SCENIUM and SCENIUM 1.1 systems, which are used for molecular imaging procedures.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Scenium 1.1 Ref K061545
Regimes: 510(k) Registry: 510(k)Scenium Ref K042863
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Siemens Molecular Imaging, Ltd. have in the registry?
The registry currently lists 2 devices for Siemens Molecular Imaging, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Siemens Molecular Imaging, Ltd.'s devices?
Among its 2 most recently registered devices, Siemens Molecular Imaging, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Siemens Molecular Imaging, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Siemens Molecular Imaging, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Siemens Molecular Imaging, Ltd. in the registry?
The most recently registered devices listed for Siemens Molecular Imaging, Ltd. include SCENIUM 1.1 and SCENIUM.