LABORATOIRE VERBIESE
FR-MF-000023445 · France · MERVILLE
LABORATOIRE VERBIESE is registered in the European database on medical devices as a manufacturer, with 59 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Fixateur de Duboscq-Brasil dans 60 ml - 20 ml
- Formol tamponné pbs 4 % - 10 ml / 40 ml
- Formol tamponné pbs 4 % - 120 ml / 180 ml
- Formol tamponné pbs 4 % - 148 ml / 180 ml
- Formol tamponné pbs 4 % - 150 ml / 250 ml
- Formol tamponné pbs 4 % - 20 ml / 60 ml
- Formol tamponné pbs 4 % - 25 ml / 60 ml
- Formol tamponné pbs 4 % - 250 ml / 500 ml
- Formol tamponné pbs 4 % - 35 ml / 60 ml
- Formol tamponné pbs 4 % - 40 ml / 60 ml
- Formol tamponné pbs 4 % - 500 ml / 1000 ml
- Formol tamponné pbs 4 % - 80 ml / 180 ml
Showing 12 of 59 declared devices.
Catalogue references include 01256_35, 01922_33, 512029_28, 512029_31, 512029_36, 512029_37.
European nomenclature codes declared: W01030705, W01030799.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 59 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 59 |
|---|---|
| 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. LABORATOIRE VERBIESE was not found in either the U.S. or the Canadian register.