Pharmpur GmbH
DE-MF-000008337 · Germany · Königsbrunn
Pharmpur GmbH is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 14 |
|---|---|
| Class IIa | 9 |
Most frequent device types declared: Packaging variant T1, Packaging variant T2, Packaging variant U1, Packaging variant U2.
Among these devices, 23 are declared sterile, 8 implantable, 1 active.
Devices declared under this manufacturer
- AddVisc
- Visco 4500
- W2O HPMC 2 %
- ophthafutur c2f6
- ophthafutur c3f8
- ophthafutur deca
- ophthafutur hpmc
- ophthafutur octa
- ophthafutur safelight
- ophthafutur sf6
- ophthafutur sil 1000
- ophthafutur sil 2000
Showing 12 of 23 declared devices.
Catalogue references include 500069, 500502, 500503, 500507, 500513, 500514.
European nomenclature codes declared: Q02030399, Q02030205, Q02030101, Q02030202, L1799.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | PHARMPUR GMBH (DE) · FDA 3005689226 |
| Devices in EUDAMED | 23 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 23 |
|---|---|
| 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: United States only. Pharmpur GmbH is registered in the United States but was not found in the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
1000276572 | issued | 2030-12-10 |
1000204102 | issued | 2030-12-10 |