GMT SARL
FR-MF-000025248 · France · Anglet
GMT SARL is registered in the European database on medical devices as a manufacturer, with 43 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Most frequent device types declared: AX300OPEN, AX300CLOSED, AX400OPEN, AX400CLOSED, CX200, CX260, CX380, CX040, Cleaner 360.5, Cleaner 360.1, Diluent 360.20, Diluent 360.5, LYA-1 Lyse 580.5, LYA-1 Lyse.
Devices declared under this manufacturer
- AUTO HEMATOLOGY ANALYZER OX - 360
- AUTO HEMATOLOGY ANALYZER OX - 560
- AUTO HEMATOLOGY ANALYZER OX 560 - RET
- AUTO HEMATOLOGY ANALYZER OX 560 - RET +
- BIOCHEMISTRY ANALYZER AX - 400CLOSED
- BIOCHEMISTRY ANALYZER AX - 400OPEN
- Coagulation Analyzer CX - 260
- DIL-A Diluent 580.20
- DIL-C Diluent 560.20
- Diluent 360.20
- Diluent 360.5
- LYA-1 Lyse
Showing 12 of 43 declared devices.
Catalogue references include AX400, OR50T0020, OX360, OX36D2000, OX36D5000, OX560RET.
European nomenclature codes declared: W0103010105, W0201010101, W0202010101, W0202020102, W0202010201, W0103010102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 43 |
| 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 | 43 |
|---|---|
| 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. GMT SARL was not found in either the U.S. or the Canadian register.