VWR International bv
BE-MF-000016952 · Belgium · Leuven
VWR International bv is registered in the European database on medical devices as a manufacturer, with 49 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 32 |
|---|
Among these devices, 17 are declared sterile.
Devices declared under this manufacturer
- CONT. 120ML PP F VACUUM TUBE IND. STERILE
- CONT. CON.120ML PP BLUE CAP STERILE
- CONT. CON.120ML PP GREEN CAP STERILE
- CONT. CON.120ML PP RED CAP IND. WRAP. STERILE
- GLOVE NITRILE AMBI LIGHT POWDERFREE L
- GLOVE NITRILE AMBI LIGHT POWDERFREE M
- GLOVE NITRILE AMBI LIGHT POWDERFREE XS
- GLOVE NITRILE PF EXTRA LIGHT XL(9-10)
- GLOVE NITRILE PF EXTRA LIGHT XS(5-6)
- VWR Latex Powder Free Gloves NC size M
- VWR Latex Powder Free Gloves NC size XS
- VWR Nitrile green gloves; M (7-8)
Showing 12 of 49 declared devices.
Catalogue references include 112-2755, 112-2765, 112-4197, 112-6644, 112-6648, 112-6649.
European nomenclature codes declared: T01020204, W05019099, T010201, W05010203, T01020201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 49 |
| Country of registration | Belgium |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 49 |
|---|---|
| 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 bv holds a Canadian licence but was not found in the U.S. register.