Selio Medical Limited
IrelandFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Selio Medical Limited have in the registry?
The registry currently lists 1 device for Selio Medical Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Selio Medical Limited's devices?
Among its 1 most recently registered device, Selio Medical Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Selio Medical Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Selio Medical Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Selio Medical Limited in the registry?
The most recently registered devices listed for Selio Medical Limited include Pre-B Seal Lung Biopsy Plug System - 15cm Model (FG0001); Pre-B Seal Lung Biopsy Plug System - 16cm Model (FG0002); Pre-B Seal Lung Biopsy Plug System - 20cm Model (FG0003).