ALPRO MEDICAL GMBH
DE-MF-000010603 · Germany · St. Georgen
ALPRO MEDICAL GMBH is registered in the European database on medical devices as a manufacturer, with 126 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 126 |
|---|
Devices declared under this manufacturer
- AlproJet-DD 1 L
- AlproJet-W 1 L
- Aspi-Jet
- BRS® (Biofilm-Removing-Set)
- IC-100 500 ml
- KDM Biodes-K Forte Eco
- MaxiWipes-L reel Nachfüllpackung
- MinutenSpray-classic 5 L
- MinutenWipes 30 StarterSet
- MinutenWipes Jumbo 50 Nachfüllpackung
- NIGHT CLEANER
- PlastiSept eco JumboWipes 30 Nachfüllpackung
Showing 12 of 126 declared devices.
Catalogue references include 19500299, 223748, 3050, 3106, 3215, 4634.
European nomenclature codes declared: D99, V0799, V80, D0799, D0299, D0599.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 126 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. ALPRO MEDICAL GMBH was not found in either the U.S. or the Canadian register.