Bloom Technologies NV
BelgiumFDA applicant, unverified
- Devices
- 1
What Bloom Technologies NV makes
Bloom Technologies NV manufactures the Bloomlife MFM-Pro, a magnetic fetal monitoring device designed for non-invasive tracking of fetal heart rate and uterine contractions during pregnancy.
The Bloomlife MFM-Pro is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Bloomlife MFM-Pro Ref K222327
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bloom Technologies NV have in the registry?
The registry currently lists 1 device for Bloom Technologies NV. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bloom Technologies NV's devices?
Among its 1 most recently registered device, Bloom Technologies NV has devices listed in FDA 510(k) (1 device).
What risk classes do Bloom Technologies NV's devices fall under?
Among its 1 most recently registered device, the classes recorded for Bloom Technologies NV's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bloom Technologies NV in the registry?
The most recently registered devices listed for Bloom Technologies NV include Bloomlife MFM-Pro.