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Cosmo Technologies

Ireland·IE-MF-000024119

Last updated September 18, 2026

About

Cosmo empowers people to live and work with confidence by innovating at the intersection of science and technology, in the spaces of MedTech AI, dermatology, gastroenterology, and contract manufacturing.

From the manufacturer's own website. Source

What Cosmo Technologies makes

Cosmo Technologies manufactures the Eleview, a medical device designed for use in dermatology and gastroenterology. The product appears to integrate imaging or diagnostic capabilities for clinical assessment in these specialties, though specific functions are not detailed.

The Eleview is classified as a Class IIa medical device and is registered in the EU via the eudamed database. The company is based in Ireland.

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 Cosmo Technologies manufacture?

Cosmo Technologies manufactures the Eleview, a medical device primarily used in dermatology and gastroenterology. The device appears to incorporate imaging or diagnostic features for clinical evaluations in these fields, though the exact functionality is not specified. The company also mentions involvement in MedTech AI and contract manufacturing, but only the Eleview is explicitly detailed as a product.

Where is Cosmo Technologies based?

Cosmo Technologies is based in Ireland. The company’s headquarters or primary operational location is in the country, which is relevant for regulatory and compliance purposes, particularly in the EU market.

Which regulatory registries list Cosmo Technologies’ devices?

Cosmo Technologies’ devices, including the Eleview, are listed in the EU’s eudamed database. This registry is used to track medical devices authorized for commercialization within the European Union, ensuring transparency and compliance with EU medical device regulations.

How are Cosmo Technologies’ devices classified under EU regulations?

The Eleview, Cosmo Technologies’ primary device, is classified as a Class IIa medical device under EU regulations. This classification indicates a moderate risk level, requiring compliance with specific design controls, clinical evaluations, and post-market surveillance to ensure safety and performance.

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

Information

Country
Ireland
Address
Riverside II, Dublin, Ireland
Facebook
—
Phone
+353 18170370
PRRC Contact
Brian Callaghan
EUDAMED SRN
IE-MF-000024119
FDA FEI Number
—
DUNS Number
—

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Eleview 9000023
EUDAMED
Class IIaActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Establishments (1)

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

  • Cosmo Technologies, Ltd. US