R. Langenbrinck GmbH
DE-MF-000025266 · Germany · Emmendingen
R. Langenbrinck GmbH is registered in the European database on medical devices as a manufacturer, with 60 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Bucket volume 2,5 Liter
- Bucket volume 5 Liter
- Bucket volume 5 Liter,
- Histology container volume 500 ml
- Histowax with added polymer
- Round tin volume 1.000 ml
- Round tin volume 500 ml
- Round tin volume 500 ml
- Screw can 500 ml volume half filled with formaldehyde 4%
- Screw can volume 1,250 ml half filled with formaldehyde 4%
- Screw can volume 1.000 ml half filled with formaldehyde 4%
- Screw can volume 2.000 ml half filled with formaldehyde 4%
Showing 12 of 60 declared devices.
Catalogue references include 08-0006/FE, 08-0006/FX, 08-0080/500FE, 08-0083/FX, 08-0103/FE, 08-0103/FX.
European nomenclature codes declared: W05020103, W05020199, W0202059016.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 60 |
| 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 | 60 |
|---|---|
| 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. R. Langenbrinck GmbH was not found in either the U.S. or the Canadian register.