humediQ global GmbH
Country not established
- Devices
- 1
What humediQ global GmbH makes
humediQ global GmbH develops radio-frequency identification (RFID) software designed for patient positioning and tracking within healthcare environments. The system integrates with hospital workflows to monitor patient locations and ensure accurate placement in medical procedures.
The company’s portfolio is regulated as Class II medical devices under FDA guidelines and is listed in the FDA’s Unique Device Identification (UDI) database. The manufacturer operates with a base in the United States.
Catalogue
- Registry: GUDID
Company details
- DUNS number
- 314128217
- [email protected]
- Phone
- +498964956284
Frequently asked questions
How many devices does humediQ global GmbH have in the registry?
The registry currently lists 1 device for humediQ global GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list humediQ global GmbH's devices?
Among its 1 most recently registered device, humediQ global GmbH has devices listed in FDA GUDID (1 device).
What risk classes do humediQ global GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for humediQ global GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from humediQ global GmbH in the registry?
The most recently registered devices listed for humediQ global GmbH include IDENTIFY 1.7.