Danmedical Limited
United KingdomFDA applicant, unverified
- Devices
- 1
What Danmedical Limited makes
Danmedical Limited manufactures the DANMEDICAL ANALYSIS SYSTEM (Model D-MAS), a diagnostic device designed for clinical analysis tasks.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the US registry.
Catalogue
Danmedical Analysis System, Model D-Mas Ref K100424
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Danmedical Limited have in the registry?
The registry currently lists 1 device for Danmedical Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Danmedical Limited's devices?
Among its 1 most recently registered device, Danmedical Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Danmedical Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Danmedical Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Danmedical Limited in the registry?
The most recently registered devices listed for Danmedical Limited include DANMEDICAL ANALYSIS SYSTEM, MODEL D-MAS.