Verum Diagnostica GmbH
GermanyFDA applicant, unverified
- Devices
- 1
What Verum Diagnostica GmbH makes
Verum Diagnostica GmbH manufactures the MULTIPLATE 5.0 AGGREGOMETER, a device used for measuring platelet aggregation in blood samples to assess coagulation function and diagnose bleeding disorders or monitor antiplatelet therapy.
The MULTIPLATE 5.0 AGGREGOMETER 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
Multiplate 5.0 Aggregometer Ref K103555
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Verum Diagnostica GmbH have in the registry?
The registry currently lists 1 device for Verum Diagnostica GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Verum Diagnostica GmbH's devices?
Among its 1 most recently registered device, Verum Diagnostica GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Verum Diagnostica GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Verum Diagnostica GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Verum Diagnostica GmbH in the registry?
The most recently registered devices listed for Verum Diagnostica GmbH include MULTIPLATE 5.0 AGGREGOMETER.