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Cirdan Imaging Ltd

Northern Ireland·XI-MF-000018019

Last updated September 18, 2026

About

Cirdan provides highly reliable, innovative LIS & imaging solutions for the acceleration & enhancement of diagnosis, optimized for pathology & clinical lab.

From the manufacturer's own website. Source

What Cirdan Imaging Ltd makes

Cirdan Imaging Ltd manufactures optical imaging devices, including the Solas OR and Solas OR XL, designed for intraoperative use in surgical settings. These systems are intended to enhance visualization of anatomical structures during procedures, particularly in orthopedic and spinal surgeries.

The company’s devices fall under EU Class A medical device classification and are registered in the EU’s eudamed database. Cirdan Imaging Ltd is based in the UK.

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 Cirdan Imaging Ltd manufacture?

Cirdan Imaging Ltd specializes in optical imaging devices, specifically the Solas OR and Solas OR XL. These systems are designed for intraoperative use, helping surgeons visualize anatomical structures more clearly during procedures like orthopedic and spinal surgeries. Their focus is on enhancing diagnostic accuracy and surgical precision in clinical settings.

Where is Cirdan Imaging Ltd based, and what region does it serve?

Cirdan Imaging Ltd is headquartered in the UK. While the company’s primary market is not explicitly stated, its devices are registered in the EU’s eudamed database, indicating compliance with European regulatory requirements. This suggests its devices are intended for use within the European Union.

Which regulatory registries list Cirdan Imaging Ltd’s devices?

Cirdan Imaging Ltd’s devices are listed in the eudamed database, which is the official EU registry for medical devices. This registry is used to track and verify the registration details of devices marketed within the European Economic Area, ensuring transparency and compliance with EU medical device regulations.

How are Cirdan Imaging Ltd’s devices classified under EU regulations?

Cirdan Imaging Ltd’s devices, including the Solas OR and Solas OR XL, are classified as EU Class A medical devices. This classification is determined based on their intended use and risk profile—optical imaging systems for intraoperative visualization are considered low-risk under EU regulations, placing them in the lowest classification tier.

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

Information

Country
Northern Ireland
Address
Riverbank, The Green, Lisburn, Northern Ireland
Phone
+44 289266 0880
PRRC Contact
Paul Matthews
EUDAMED SRN
XI-MF-000018019
FDA FEI Number
—
DUNS Number
—

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
Solas OR A4120
EUDAMED
Class AActive
Solas OR XL A4120XL
EUDAMED
Class AActive

Related Companies

Authorised Representatives

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Importers

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Authorities

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FDA Establishments (2)

Establishments registered with the FDA under this company group, matched by name.

  • Cirdan Imaging Limited Lisburn Antrim and Newtownabbey · GB FEI 3010478247
  • Cirdan Imaging Limited US