Better Medicine OÜ
Estonia EE-MF-000034185 Last updated 17 Sep 2026
- Devices
- 1
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
BMVision Kidney Ref BMV-KIDNEY
EUDAMED certificates
Notified body 2797 1 certificate
- MDR 795177 Issued
Quality management system EU MDR
- Issued
- 6 Dec 2024
- Expires
- 5 Dec 2029
Related companies
Notified bodies
- Notified body 2797
About
Utilising AI to transform cancer diagnostics and radiology workflows for improved efficiency and patient outcomes.
What Better Medicine OÜ makes
Better Medicine OÜ manufactures the BMVision Kidney, a medical imaging device designed for kidney assessment and diagnostic analysis. This product is intended for use in radiology workflows to support clinical decision-making regarding kidney-related conditions.
The BMVision Kidney is classified as a Class IIa medical device and is registered in the EU’s eudamed database. The company is based in Estonia.
Frequently asked questions
What types of medical devices does Better Medicine OÜ manufacture?
Better Medicine OÜ manufactures the BMVision Kidney, a medical imaging device specifically designed for kidney assessment and diagnostic analysis. This device is intended to assist radiologists and clinicians in evaluating kidney-related conditions, thereby supporting more informed clinical decision-making.
Where is Better Medicine OÜ based?
Better Medicine OÜ is based in Estonia, as indicated by its company registration details. The location is relevant for understanding regulatory jurisdiction and compliance requirements for its medical devices.
Which regulatory registries list Better Medicine OÜ’s devices?
Better Medicine OÜ’s devices, including the BMVision Kidney, are listed in the EU’s eudamed database. This registry is used to track medical devices within the European Union, ensuring transparency and traceability for regulatory oversight.
How are Better Medicine OÜ’s devices classified under EU regulations?
The BMVision Kidney, the primary device manufactured by Better Medicine OÜ, is classified as a Class IIa medical device. This classification is determined by its intended purpose and associated risks, with Class IIa devices requiring conformity assessment procedures to ensure safety and performance before market placement.
Information
- Country
- Estonia
- Address
- 9, Narva maantee, Tartu, Estonia
- Website
- www.bettermedicine.ai/
- [email protected]
- PRRC contact
- Kadri Tõnnisson
- EUDAMED SRN
- EE-MF-000034185