COMED SAS
FR-MF-000000151 · France · STRASBOURG
COMED SAS is registered in the European database on medical devices as a manufacturer, with 110 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 110 |
|---|
Devices declared under this manufacturer
- Cache œil
- Pied à sérum
- Pied à sérum blanc Hémodia
- Spéculums auriculaires à usage unique
- Test d'acuité visuelle
- Tige porte sérum 2 crochets inox
- Tige porte sérum 2 crochets inox 1m50
- Tige porte sérum 2 crochets plastique
- Tige porte sérum 4 crochets inox
Showing 12 of 110 declared devices.
Catalogue references include 24 701 25B, 2470025ACV, 2470025AL, 2470025BCJD, 2470025BCJM, 2470040BL.
European nomenclature codes declared: Z12149085, Z12030399, Z12120199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 110 |
| 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 | 110 |
|---|---|
| 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. COMED SAS was not found in either the U.S. or the Canadian register.