Lück GmbH & Co. KG
DE-MF-000015002 · Germany · Bocholt
Lück GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 331 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 331 |
|---|
Devices declared under this manufacturer
- Lagerungskissen Rhombo-fill
- Lagerungskissen Rhombo-med
- Matratze 90x200x12 vis 4+8 PU
- Matratze 90x200x14 ks PU
- Matratze IQCare Deku3
- Matratze P1
- Matratze Rhombo-Care (Sky) Therm Plus
- Matratze Rhombo-Care (Sky) Therm Plus \
- Matratze Rhombo-Care Prevent Plus
- Matratze Rhombo-Care Therm
- Matratze Rhombo-Care Therm ECO
- Matratze Rhomo-Care (Sky) Therm Plus \
Showing 12 of 331 declared devices.
Catalogue references include 19.348, 19.763, 222941, 25.744, 25.759, 26.762.
European nomenclature codes declared: V080702, V08030102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 331 |
| 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 | 331 |
|---|---|
| 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. Lück GmbH & Co. KG was not found in either the U.S. or the Canadian register.