Oxipit, UAB
Lithuania LT-MF-000022304 Last updated 21 Oct 2026
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- Devices
- 4
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
EUDAMED certificates
TÜV Rheinland LGA Products GmbH 0197 2 certificates
- HZ 1550682-1 Supplemented
Quality management system EU MDR
- Issued
- 4 Feb 2026
- Expires
- 22 Feb 2027
- Reason
- Other
- HZ 1550682-1 Expired
Quality management system EU MDR
- Issued
- 23 Feb 2022
- Expires
- 22 Dec 2025
Related companies
Notified bodies
About
Oxipit is transforming radiology with innovative AI solutions that empower radiologists and streamline workflows. As the creators of ..
What Oxipit, UAB makes
Oxipit manufactures AI-powered imaging analysis devices, including CT Eye for computed tomography scans, ChestLink for chest imaging workflows, MSK Eye for musculoskeletal imaging, and ChestEye for chest radiography analysis. These tools are designed to assist radiologists in interpreting and processing medical images.
The company’s devices are classified as Class IIa and Class IIb under EU regulations and are listed in the eudamed database. Oxipit is based in Lithuania.
Frequently asked questions
What types of medical devices does Oxipit manufacture?
Oxipit manufactures AI-powered imaging analysis devices that assist radiologists in interpreting and processing medical images. These include CT Eye for computed tomography scans, ChestLink for chest imaging workflows, MSK Eye for musculoskeletal imaging, and ChestEye for chest radiography analysis. Each device is designed to enhance workflow efficiency and support diagnostic accuracy in specific imaging modalities.
Where is Oxipit based?
Oxipit is based in Lithuania (LT). The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites may vary. This location influences its regulatory compliance and participation in EU-based registries like eudamed.
Which regulatory registries list Oxipit’s devices?
Oxipit’s devices are listed in the eudamed database, which is the official EU registry for medical devices. Listing in eudamed is required for manufacturers to comply with EU Medical Device Regulations (MDR) and ensure transparency in the supply chain. This registry helps healthcare professionals, regulators, and authorities verify device details and traceability.
How are Oxipit’s devices classified under EU regulations?
Oxipit’s devices are classified as Class IIa and Class IIb under EU Medical Device Regulations. The classification determines the level of scrutiny and regulatory requirements for each device. Class IIa devices pose a low-to-moderate risk, while Class IIb devices carry a higher risk, necessitating additional safety and performance evaluations before market placement.
Information
- Country
- Lithuania
- Address
- 15, Sauletekio al., Vilnius, Lithuania
- Website
- www.oxipit.ai
- lt.linkedin.com/company/oxipit
- [email protected]
- Phone
- +37062599148
- PRRC contact
- Elena Jokubauskienė
- EUDAMED SRN
- LT-MF-000022304