LD Medicare
FR-MF-000049573 · France · Pamiers
LD Medicare is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 7 |
|---|
Most frequent device types declared: Dermokat, Neorig® Urétéro – Tubulure irrigation 1 voie pour urétéroscopie.
Among these devices, 7 are declared sterile.
Devices declared under this manufacturer
- ASPIRATION SET
- Dermokat Protective Dressing Standard
- IRRIGATION SET DOUBLE WAY
- IRRIGATION SET SIMPLE WAY
- IRRIGATION SET URETEROSCOPY DOUBLE WAY
- Irrigation set Ureteroscopy
- Y IRRIGATION SET
Catalogue references include 750016, 750026, 750036, 750046, 750076, 750096.
European nomenclature codes declared: Z12019007, C03010403, M04010202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| 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 | 7 |
|---|---|
| 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. LD Medicare was not found in either the U.S. or the Canadian register.