Ecolab Deutschland GmbH
DE-MF-000004932 · Germany · Monheim am Rhein
Ecolab Deutschland GmbH is registered in the European database on medical devices as a manufacturer, with 119 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 46 |
|---|---|
| Class IIa | 73 |
Devices declared under this manufacturer
- ANIOS NDT
- CITROCLOREX 2% MD
- INCIDIN LIQUID
- INCIDIN PRO
- Incidin OxyWipe S
- Incidin Oxyfoam S
- OLYMPUS DISINFECTANT
- OLYMPUS ENDOACT
- OLYMPUS ENDODIS
- Olympus EndoDis Pro
- SEKUMATIC FNZ
- SEKUMATIC NDT
Showing 12 of 119 declared devices.
Catalogue references include 3023500, 3050590, 3056690, 3092580, 3115810, 3116060.
European nomenclature codes declared: D0901, V0799, D0799, D0599, D050103, D99.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 119 |
| 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 | 118 |
|---|---|
| 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. Ecolab Deutschland GmbH was not found in either the U.S. or the Canadian register.