VWR INTERNATIONAL SAS
FR-MF-000016509 · France · Rosny-Sous-Bois
VWR INTERNATIONAL SAS is registered in the European database on medical devices as a manufacturer, with 301 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 7 |
|---|
Devices declared under this manufacturer
- Coverquick 1000 Q Path
- Formaldehyde 4% Q Path / FORMALINE 10%
- Q Path Containers 150 mL White cap
- Q Path Macrostar I
- Q Path Macrostar II - rack of 40
- Q Path Macrostar III
- Q Path Macrostar V
- Q Path Macrostar V - rack of 40
- Q Path Microstar II
- Q Path Microstar II - rack of 40
- Q Path Microstar III
- Q Path Microstar V
Showing 12 of 301 declared devices.
Catalogue references include 05547528, 10.06025BL0001, 720-2165, 720-2192, 720-2243, 720-2407.
European nomenclature codes declared: W05030501, W01030705, W01030708, W01030706, W05020103, U09030301.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 301 |
| 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 | 301 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | VWR INTERNATIONAL |
North American profile: Canada only. VWR INTERNATIONAL SAS holds a Canadian licence but was not found in the U.S. register.