Dune Medical Devices Ltd
Country not established
- Devices
- 1
What Dune Medical Devices Ltd makes
Dune Medical Devices Ltd manufactures intraoperative tumour margin analysis probes, designed to assist surgeons in identifying cancerous tissue margins during surgical procedures. The MarginProbe® Probe is used to provide real-time feedback on tissue characteristics to improve precision in tumour resection.
The company’s products fall under Class III medical devices, indicating they carry the highest regulatory risk due to their critical role in patient safety. These devices are listed in the FDA’s Unique Device Identifier (UDI) database, adhering to U.S. regulatory requirements for tracking and compliance. The manufacturer is based in the United States.
Catalogue
- GUDID
Company details
- DUNS number
- 533247359
Frequently asked questions
How many devices does DUNE MEDICAL DEVICES LTD have in the registry?
The registry currently lists 1 device for DUNE MEDICAL DEVICES LTD. Devices recorded under merged duplicate company entries are counted once.
Which registries list DUNE MEDICAL DEVICES LTD's devices?
Among its 1 most recently registered device, DUNE MEDICAL DEVICES LTD has devices listed in FDA GUDID (1 device).
What risk classes do DUNE MEDICAL DEVICES LTD's devices fall under?
Among its 1 most recently registered device, the classes recorded for DUNE MEDICAL DEVICES LTD's devices are Class III. Each device page shows its own class and authorisation.
What are the newest devices from DUNE MEDICAL DEVICES LTD in the registry?
The most recently registered devices listed for DUNE MEDICAL DEVICES LTD include MarginProbe® Probe AC0300001.