Etablissements Albert Legrand
FR-MF-000029888 · France · Paris
Etablissements Albert Legrand is registered in the European database on medical devices as a manufacturer, with 29 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 29 |
|---|
Among these devices, 1 are declared active.
Devices declared under this manufacturer
- Anuscope XL bord biseauté sans poignée à usage unique
- Anuscope XL à bord droit sans poignée à usage unique
- Anuscope adulte bord biseauté avec poignée à usage unique
- Anuscope adulte bord biseauté sans poignée à usage unique
- Anuscope adulte long à bord droit avec poignée à usage unique
- Anuscope adulte long à bord droit sans poignée à usage unique
- Anuscope pédiatrique bord biseauté avec poignée à usage unique
- Anuscope pédiatrique bord biseauté sans poignée à usage unique
- Anuscope pédiatrique à bord droit avec poignée à usage unique
- Anuscope pédiatrique à bord droit sans poignée à usage unique
- Ligateur LigaConfort standard à usage unique
- Ligateur XL à poignée à usage unique
Showing 12 of 29 declared devices.
Catalogue references include 07-AUL-17/1, 07-AUL-22/1, 07-AUP-17/1, 07-AUP-22/1, 07-Liganet/1, 12.080/1.
European nomenclature codes declared: G02060301, G020401, Z12020605, G020401,G02060301, G02060301,Z12020605.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 29 |
| 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 | 29 |
|---|---|
| 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. Etablissements Albert Legrand was not found in either the U.S. or the Canadian register.