Pharma Aldenhoven GmbH & Co. KG
DE-MF-000005322 · Germany · Aldenhoven
Pharma Aldenhoven GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Most frequent device types declared: Kopfschmerz Roll-On.
Devices declared under this manufacturer
- Altapharma Kopfschmerz Roll-On
- BI LIFE Kopfschmerz Roll-On
- Curafit Plus Kopfschmerz Roll-On
- Mivolis Abschwellendes Nasenspray
- Mivolis Meerwasser Nasenspray
- Mivolis Meerwasser Nasenspray sensitiv
- Mivolis Meerwasser Schnupfenspray
- SilaVit Kopfschmerz Roll-On
- SoVita Kopfschmerz Roll-On
Catalogue references include 003031, 004012, 004013, 004015, 004016, 004405.
European nomenclature codes declared: V9099, Q030103.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| 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: Neither register. Pharma Aldenhoven GmbH & Co. KG was not found in either the U.S. or the Canadian register.