ADL Anti Dekubitus Lagerungssyteme GmbH
DE-MF-000017900 · Germany · Amt Wachsenburg
ADL Anti Dekubitus Lagerungssyteme GmbH is registered in the European database on medical devices as a manufacturer, with 95 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 95 |
|---|
Most frequent device types declared: ADL Viskoschaum Sitzkissen, Arthrodesenkissen, Objektmatratze RG 35, Objektmatratze RG 40, Olymp PU.
Among these devices, 4 are declared active.
Devices declared under this manufacturer
- ADL 200
- ADL Viskoschaum Sitzkissen
- Arthrodesenkissen
- Clinisan®
- Clinisan® plus
- Easy Mat
- Objektmatratze RG 35
- Objektmatratze RG40
- Olymp
- Silflex 200
- Silflex 400
- Standardmatratze RG 35
Showing 12 of 95 declared devices.
Catalogue references include 00100700, 00100710, 00110483-FO, 00110485-FO, 00160750, 00180280.
European nomenclature codes declared: V080702, V08030102, V080701, V080399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 95 |
| 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 | 95 |
|---|---|
| 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. ADL Anti Dekubitus Lagerungssyteme GmbH was not found in either the U.S. or the Canadian register.