Igefa Handelsgesellschaft mbH & Co. KG
DE-MF-000029971 · Germany · Ahrensfelde OT Blumberg
Igefa Handelsgesellschaft mbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 56 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 56 |
|---|
Devices declared under this manufacturer
- Kolibri combed PREMIUM ultra 60x60cm
- Kolibri comfort PREMIUM maxi
- Kolibri comfort PREMIUM men 2
- Kolibri comfort SOFT maxi
- Kolibri compact PREMIUM classic
- Kolibri compact PREMIUM supra
- Kolibri compact PREMIUM ultra
- Kolibri comslip PREMIUM supra L/XL
- Kolibri comslip PREMIUM supra M
- Kolibri comslip PREMIUM ultra L/XL
- Kolibri comslip SOFT ultra XL
- Kolibri comtrain PREMIUM extra M
Showing 12 of 56 declared devices.
Catalogue references include 2108219, 2108221, 2117265, 2135603, 2135607, 2142801.
European nomenclature codes declared: T04010103, T04010102, T04010101, T04010201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 56 |
| 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 | 56 |
|---|---|
| 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. Igefa Handelsgesellschaft mbH & Co. KG was not found in either the U.S. or the Canadian register.