Cosmo Technologies
Ireland IE-MF-000024119 Last updated 21 Oct 2026
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- Devices
- 1
- Registries
- EUDAMEDFDA
- FDA recalls
- 0
Catalogue
Eleview Ref 9000023
FDA establishments
- Cosmo Technologies, Ltd. IE
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.
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.
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.
Information
- Country
- Ireland
- Address
- Riverside II, Dublin, Ireland
- Website
- www.cosmopharma.com
- [email protected]
- Phone
- +353 18170370
- PRRC contact
- Brian Callaghan
- EUDAMED SRN
- IE-MF-000024119