LID - SOTRAMET
FR-MF-000014659 · France · Grans
LID - SOTRAMET is registered in the European database on medical devices as a manufacturer, with 140 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 140 |
|---|
Most frequent device types declared: SUPPORT PLATE WHITE.
Devices declared under this manufacturer
- BELLON CEILING
- BELLON CEILING WITH BALL JOINT LED18PH-G
- Bella Lumax rotative
- CARLA
- CARLA FOCUS
- CLAMP FOR MEDICAL RAIL
- DIANA
- HYDRA
- LINA
- LISA
- Pied roulant
- SUPPORT PLATE WHITE
Showing 12 of 140 declared devices.
Catalogue references include BOR50651BL, ETRPM007, LED18P, LED22650R, LEDB0900ISC, LEDBI122-ISC.
European nomenclature codes declared: Z12010702, Z12010701.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 140 |
| 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 | 140 |
|---|---|
| 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. LID - SOTRAMET was not found in either the U.S. or the Canadian register.