Imtegra GmbH & Co KG
DE-MF-000006451 · Germany · Rostock
Imtegra GmbH & Co KG is registered in the European database on medical devices as a manufacturer, with 122 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 122 |
|---|
Among these devices, 58 are declared sterile.
Devices declared under this manufacturer
- Absorba
Showing 12 of 122 declared devices.
Catalogue references include 2206 3201, 2206 4202, 2206 4208, 2206 5002, 2207 5014, 3105.
European nomenclature codes declared: T020199, T030199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 122 |
| 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 | 122 |
|---|---|
| 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. Imtegra GmbH & Co KG was not found in either the U.S. or the Canadian register.