ID SOLUTIONS
FR-MF-000024876 · France · Montpellier
ID SOLUTIONS is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- IDTM SARS-CoV-2/Influenza Triplex
- IDTM SARS-CoV-2/Influenza TriplexIDTM SARS-CoV-2/Influenza Triplex
- iSolutions™ Enteric Bacteria & C. difficile Fullplex qPCR
- iSolutions™ Enteric Virus Fullplex qPCR
- iSolutions™ Essential Enteric Bacteria Fullplex qPCR
Catalogue references include IDRESPI-P1-100 (FR) - Boîtes, IDRESPI-P1-500 (FR) - Boîtes, IS-ENTBAC-100 (FR) - Boîtes, IS-ENTBAC-CD-100 (FR) - Boîtes, IS-ENTVIR-100 (FR) - Boîtes.
European nomenclature codes declared: W0105070201, W0105040519, W0105070302, W0105041106.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 5 |
|---|---|
| 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. ID SOLUTIONS was not found in either the U.S. or the Canadian register.