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Oxipit, UAB

Lithuania LT-MF-000022304 Last updated 21 Oct 2026

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Devices
4
Registries
EUDAMED
FDA recalls
0

Catalogue4

  • CT Eye Ref 1

    Class IIb EUDAMED Active
  • ChestLink Ref 1

    Class IIb EUDAMED Active
  • MSK Eye Ref 1

    Class IIb EUDAMED Active
  • ChestEye Ref 1

    Class IIa EUDAMED Active

EUDAMED certificates2

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (2)

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

About

Oxipit is transforming radiology with innovative AI solutions that empower radiologists and streamline workflows. As the creators of ..

From the manufacturer's own website. Source

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.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

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.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Lithuania
Address
15, Sauletekio al., Vilnius, Lithuania
Website
www.oxipit.ai
Phone
+37062599148
PRRC contact
Elena Jokubauskienė
EUDAMED SRN
LT-MF-000022304