LAURYPATH
FR-MF-000020948 · France · CHAPONOST
LAURYPATH is registered in the European database on medical devices as a manufacturer, with 83 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- 10% Neutral Buffered Formalin 125/60 ML - YELLOW CAPS (x24)
- 10% Neutral Buffered Formalin 180/80 ML - YELLOW CAPS (x24)
- 10% PINK-Fix Formalin 20/10ML - YELLOW CAPS (x24)
- 10% PINK-Fix Formalin 5 L (x 4)
- 70% Dehydrant
- BIDON 10L FORMALDEHYDE 4% pH7
- BIDON 5L FORMALDEHYDE ROSE 4% PH7
- FLACON 20/10ML DE FORMALDEHYDE ROSE 4% pH7 - CAPE JAUNE (
- FLACON 40/20ML DE FORMALDEHYDE 4% pH7 - CAPE ROUGE
- FLACON 40/20ML DE FORMALDEHYDE 4% pH7 - CAPE VERTE
- FLACON 60/30ML DE FORMALDEHYDE ROSE 4% pH7 - CAPE BLEUE
- POT 500/250ML FORMALDEHYDE 4% pH7
Showing 12 of 83 declared devices.
Catalogue references include 40877-02/10R, 40877-04/20EV, 40877-36R-MMF, 40877-41, 51201P-LP-Y, 5735P-LP.
European nomenclature codes declared: W01030705, W0102090207, W01030799.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 83 |
| 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 | 83 |
|---|---|
| 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. LAURYPATH was not found in either the U.S. or the Canadian register.