DocCheck Steam GmbH
DE-MF-000050235 · Germany · Köln
DocCheck Steam GmbH is registered in the European database on medical devices as a manufacturer, with 64 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 64 |
|---|
Most frequent device types declared: Clôppe.
Among these devices, 4 are declared active.
Devices declared under this manufacturer
- Antimikrobielle Kupfermembran \
- Clôppe
- Clôppe Pro
- Lûx
- Scaut
- Tŭlip
- Tŭlip Clean
- Tŭlip HiFi
- Vibe
Showing 12 of 64 declared devices.
Catalogue references include 101963.6, 102703.1, 102853.4, 103096.12, 103395.1, 104360.1.
European nomenclature codes declared: C9005, L160101, N010199, Z12040118, V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 64 |
| 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 | 64 |
|---|---|
| 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. DocCheck Steam GmbH was not found in either the U.S. or the Canadian register.