ALLERGIKA Pharma GmbH
DE-MF-000016908 · Germany · Wolfratshausen
ALLERGIKA Pharma GmbH is registered in the European database on medical devices as a manufacturer, with 74 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 74 |
|---|
Catalogue references include 1414, 1415, 1417, 1420, 1427, 1477.
European nomenclature codes declared: T0299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 74 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 74 |
|---|---|
| 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. ALLERGIKA Pharma GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
44911230005 | issued | 2031-05-06 |