Paxeramed
Country not established
- Devices
- 1
What Paxeramed makes
Paxeramed manufactures the PAXERAPACS, a medical device designed for the storage and retrieval of radiographic images in healthcare settings, enabling efficient digital archiving and distribution of X-ray and other imaging data.
The PAXERAPACS is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Paxerapacs Ref K132586
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Paxeramed have in the registry?
The registry currently lists 1 device for Paxeramed. Devices recorded under merged duplicate company entries are counted once.
Which registries list Paxeramed's devices?
Among its 1 most recently registered device, Paxeramed has devices listed in FDA 510(k) (1 device).
What risk classes do Paxeramed's devices fall under?
Among its 1 most recently registered device, the classes recorded for Paxeramed's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Paxeramed in the registry?
The most recently registered devices listed for Paxeramed include PAXERAPACS.