Medilink A/S
DenmarkFDA applicant, unverified
- Devices
- 1
What Medilink A/S makes
Medilink A/S manufactures Hydrozid, a medical device designed for [specific clinical purpose or application—if not clear, omit detail]. This product falls under Class II devices, indicating moderate risk and regulatory oversight.
Hydrozid is authorised via the FDA’s 510(k) pathway and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Hydrozid Ref K201740
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medilink A/S have in the registry?
The registry currently lists 1 device for Medilink A/S. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medilink A/S's devices?
Among its 1 most recently registered device, Medilink A/S has devices listed in FDA 510(k) (1 device).
What risk classes do Medilink A/S's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medilink A/S's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medilink A/S in the registry?
The most recently registered devices listed for Medilink A/S include Hydrozid.