RAL Diagnostics
FR-MF-000007902 · France · MARTILLAC
RAL Diagnostics is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Devices declared under this manufacturer
- BLEU-RAL 555
- BLUE-RAL 555
- Carbolic gentian violet
- EOSIN-RAL 555
- FIX-RAL 555
- Giemsa R solution
- May-Grünwald solution
- RAL Diff-Quik™ solution I
- RAL Diff-Quik™ solution II
- Tampon pH=7.0 (1 dose)
Showing 12 of 27 declared devices.
Catalogue references include 320965-0200, 361640-0100, 361650-1000, 361650-2500, 362870-0100, 362870-0500.
European nomenclature codes declared: W0103010399, W0104010804, W0103010302, W0104010899.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | RAL DIAGNOSTICS (FR) · FDA 3009000266 |
| Devices in EUDAMED | 27 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 27 |
|---|---|
| Found in the U.S. device database | 2 |
| Share | 7.4 % |
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. RAL Diagnostics is registered in the United States but was not found in the Canadian register.