European Pharma Group B.V.
NL-MF-000021390 · Netherlands · Schiphol-Rijk
European Pharma Group B.V. is registered in the European database on medical devices as a manufacturer, with 42 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 24 |
|---|---|
| Class IIa | 18 |
Most frequent device types declared: Model M, S.
Among these devices, 30 are declared sterile, 24 active, 24 with a measuring function.
Devices declared under this manufacturer
- Adaptor de 10ml
- Adaptor de 3ml
- Duza InsuJet™
- Injector InsuJet™ V5
- InsuJet™ 10ml Adaptor
- InsuJet™ 3ml Adaptor with Cartridge Holder
- InsuJet™ Injector V5
- InsuJet™ Nozzle
- InsuJet™ Nozzle with Comfort Ring
- InsuJet™ Starter Pack V5
- InsuJet™ Starter pack V5
- InsuJet™ V5 Kit de Inceput
Showing 12 of 42 declared devices.
Catalogue references include 0120090105S, 0120090205S, 01300902050S, 013009RO050M, 017000RO0305, 017100RO0305.
European nomenclature codes declared: A99.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 42 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 42 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | EUROPEAN PHARMA GROUP B.V. |
North American profile: Canada only. European Pharma Group B.V. holds a Canadian licence but was not found in the U.S. register.