Mrlguidance B.V.
NetherlandsFDA applicant, unverified
- Devices
- 1
What Mrlguidance B.V. makes
Mrlguidance B.V. manufactures the BoneMRI v1.4, a medical imaging device designed for magnetic resonance imaging of bone structures, enabling detailed visualization for diagnostic purposes.
The BoneMRI v1.4 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
BoneMRI v1.4 Ref K221762
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mrlguidance B.V. have in the registry?
The registry currently lists 1 device for Mrlguidance B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mrlguidance B.V.'s devices?
Among its 1 most recently registered device, Mrlguidance B.V. has devices listed in FDA 510(k) (1 device).
What risk classes do Mrlguidance B.V.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mrlguidance B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mrlguidance B.V. in the registry?
The most recently registered devices listed for Mrlguidance B.V. include BoneMRI v1.4.