Börm Bruckmeier Verlag GmbH
DE-MF-000013053 · Germany · Grünwald
Börm Bruckmeier Verlag GmbH is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|
Most frequent device types declared: BB Content App, Medimir — Clinical Decision Support System.
Among these devices, 8 are declared active.
Devices declared under this manufacturer
- Arzneimittel Pocket
- DGK Pocket Leitlinien
- EAU Guidelines App
- Medimir
- Neuro CDS
- Onco CDS
- Pneumo CDS
- Rheuma CDS
Catalogue references include Arzneimittel Pocket, DGK Pocket Leitlinien, EAU Guidelines App, Medimir v2.2, Neuro CDS, Onco CDS.
European nomenclature codes declared: V92.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| 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 | 8 |
|---|---|
| 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. Börm Bruckmeier Verlag GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G10 097893 0004 | reinstated | 2028-06-25 |