Mirai Medical Limited
IE-MF-000002374 · Ireland · Galway
Mirai Medical Limited is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 4 |
|---|---|
| Class IIb | 1 |
Most frequent device types declared: 700209, 700245, MMHT1.
Among these devices, 2 are declared sterile, 3 reusable, 5 active.
Devices declared under this manufacturer
- CUTIS
- EPORE Generator
- EndoVE
Catalogue references include 700209, 700245, MMHT1.
European nomenclature codes declared: Z12040299, Z12040285.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| Country of registration | Ireland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 5 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Mirai Medical Limited was not found in either the U.S. or the Canadian register.