Medigard Limited
Country not established
- Devices
- 1
What Medigard Limited makes
Medigard Limited manufactures blood collection devices designed for medical use, facilitating the safe and efficient collection of blood samples in clinical settings.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Medigard Blood Collection Device Ref K082511
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medigard Limited have in the registry?
The registry currently lists 1 device for Medigard Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medigard Limited's devices?
Among its 1 most recently registered device, Medigard Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Medigard Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medigard Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medigard Limited in the registry?
The most recently registered devices listed for Medigard Limited include MEDIGARD BLOOD COLLECTION DEVICE.