Medtro GmbH
Country not established
- Devices
- 1
What Medtro GmbH makes
Medtro GmbH manufactures the THROMBO-TEST, a device designed for assessing thrombus formation or clot detection in laboratory settings.
The THROMBO-TEST is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Thrombo-Test (X) Ref K801054
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtro GmbH have in the registry?
The registry currently lists 1 device for Medtro GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtro GmbH's devices?
Among its 1 most recently registered device, Medtro GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Medtro GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtro GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtro GmbH in the registry?
The most recently registered devices listed for Medtro GmbH include THROMBO-TEST (X).