BRUMABA GmbH
DE-MF-000006236 · Germany · Geretsried
BRUMABA GmbH is registered in the European database on medical devices as a manufacturer, with 28 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 28 |
|---|
Most frequent device types declared: BRUMABA Caddy, BRUMABA Operating Table, BRUMABA treatment table.
Among these devices, 28 are declared active.
Devices declared under this manufacturer
- BRUMABA CL Genius - STA
- BRUMABA CL Genius Eye - DTN
- BRUMABA CL Genius Eye - STA
- BRUMABA CL Genius Eye Pro - DTA
- BRUMABA CL Genius Eye Pro - STA
- BRUMABA CL Genius XL STN
- BRUMABA Ecura
- BRUMABA Genius Eye Z - STA
- BRUMABA OP O2 Primus-N
- BRUMABA OP O2 Varius
- BRUMABA OP O2 Varius-N
- BRUMABA Venus DTA
Showing 12 of 28 declared devices.
Catalogue references include C1.01.13, G4.12.23, O2.11.31, O2.12.31, V1.02.12, Y1.02.12.
European nomenclature codes declared: Z12011202, Z12019010, V08060199.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | BRUMABA GmbH & Co.KG (DE) · FDA 3005607354 |
| Devices in EUDAMED | 28 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 28 |
|---|---|
| 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: United States only. BRUMABA GmbH is registered in the United States but was not found in the Canadian register.