CHROMagar™
FR-MF-000024723 · France · La Plaine Saint Denis
CHROMagar™ is registered in the European database on medical devices as a manufacturer, with 80 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Devices declared under this manufacturer
- CHROMagar™ Acinetobacter Base
- CHROMagar™ C.difficile base
- CHROMagar™ COL-APSE supplement
- CHROMagar™ Campylobacter base
- CHROMagar™ KPC supplement
- CHROMagar™ MRSA Base A
- CHROMagar™ MRSA Mix C
- CHROMagar™ StrepA base
- CHROMagar™ StrepA-S1
- CHROMagar™ StrepA-S2
- CHROMagar™ StrepB base
- CHROMagar™ mSuperCARBA™ base
Showing 12 of 80 declared devices.
Catalogue references include AC092(B), CO262(S), CP572(B), KP102, MR513-125(C), SB282(B).
European nomenclature codes declared: W0104010104, W0104010101, W0104030101.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | CHROMAGAR (FR) · FDA 9680687 |
| Devices in EUDAMED | 80 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 80 |
|---|---|
| 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: United States only. CHROMagar™ is registered in the United States but was not found in the Canadian register.