Kurland GmbH
DE-MF-000010484 · Germany · Ainring
Kurland GmbH is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 15 |
|---|
Devices declared under this manufacturer
- Einmal Heu-Kräuterpackung
- Einmal Heusack, ascend
- Einmal Naturmoorpackung
- Einmal-Lehmpackung
- Heat Carrier, half width
- Heubad, 60 x 80 cm
- Heusack für Nacken & Schulter
- Heusack klein
- Heusäcke, mittel
- Klassische Moorpackung
- Sole Tücher
- Wärmeträger, Größe I
Showing 12 of 15 declared devices.
Catalogue references include 10140-201, 10400-201, 10401-204, 10401-241, 10430-050, 10820-xxxxx.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 15 |
| 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 | 15 |
|---|---|
| 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. Kurland GmbH was not found in either the U.S. or the Canadian register.