OACP IE LTD
IE-MF-000003506 · Ireland · Clonakilty
OACP IE LTD is registered in the European database on medical devices as a manufacturer, with 162 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: FP-005, FP-013, FP-022, FP-028, FP-033.
Catalogue references include 031114-DO, FP-005, FP-013, FP-022 (FP-206-1), FP-028, FP-033.
European nomenclature codes declared: W01030703, W05019002, W02050199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 162 |
| 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 | 7 |
|---|---|
| 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. OACP IE LTD was not found in either the U.S. or the Canadian register.