Mediwatch Plc
United KingdomFDA 510(k) applicant, unverified
- Devices
- 1
What Mediwatch Plc makes
Mediwatch Plc manufactures the PortaScan Bladder Scanner (Model PA00146), a handheld ultrasound device designed for non-invasive bladder volume measurement to monitor fluid intake and output in clinical settings.
The company’s portfolio is regulated under FDA’s Class II device classification, with the PortaScan Bladder Scanner listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Portascan Bladder Scanner, Model PA00146 Ref K033906
510(k) 510(k)
Frequently asked questions
How many devices does Mediwatch Plc have in the registry?
The registry currently lists 1 device for Mediwatch Plc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mediwatch Plc's devices?
Among its 1 most recently registered device, Mediwatch Plc has devices listed in FDA 510(k) (1 device).
What risk classes do Mediwatch Plc's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mediwatch Plc's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mediwatch Plc in the registry?
The most recently registered devices listed for Mediwatch Plc include PORTASCAN BLADDER SCANNER, MODEL PA00146.