Burmeier GmbH & Co. KG
DE-MF-000010563 · Germany · Hiddenhausen
Burmeier GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 20 |
|---|
Most frequent device types declared: Allura II 100, Allura II 120, Dali, Gigant, Inovia.
Among these devices, 20 are declared active.
Devices declared under this manufacturer
- Allura II 100 (standard)
- Allura II 120 (standard)
- Dali (econ)
- Dali (economic)
- Dali (low-entry-econ)
- Dali (standard)
- Dali (wash)
- Gigant (standard)
- Inovia (standard)
- Lippe IV (standard)
- Regia (standard)
- Regia movo
Showing 12 of 20 declared devices.
Catalogue references include 229911, 232118, 238647, 262626, 285870, 287090.
European nomenclature codes declared: V08060101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 20 |
| 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 | 20 |
|---|---|
| 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. Burmeier GmbH & Co. KG was not found in either the U.S. or the Canadian register.