Mediwatch, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Mediwatch, Ltd. makes
Mediwatch, Ltd. manufactures ultrasound systems, including the Multiscan Ultrasound Scanner (Model M0002) and the Multiscan Ultrasound System (Model M0001), designed for diagnostic imaging.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mediwatch, Ltd. have in the registry?
The registry currently lists 1 device for Mediwatch, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mediwatch, Ltd.'s devices?
Among its 1 most recently registered device, Mediwatch, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Mediwatch, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mediwatch, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mediwatch, Ltd. in the registry?
The most recently registered devices listed for Mediwatch, Ltd. include MEDIWATCH MULTISCAN ULTRASOUND SYSTEM/SCANNER, MODEL M0002 (SCANNER ONLY); MULTISCAN ULTRASOUND SYSTEM, MODEL M0001.