Anton Hübner GmbH & Co. KG
DE-MF-000006418 · Germany · Ehrenkirchen
Anton Hübner GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|---|
| Class IIb | 5 |
Most frequent device types declared: Emery Boards.
Devices declared under this manufacturer
- ACTIVOX Compressed lozenge
- ACTIVOX SPRAY NASAL
- ACTIVOX® Spray Nasal
- ARKOTOUX Sirop
- Arkovox Spray Nasal
- Nasenadapter für Provokationslösung
- Panthenol Meerwasser Nasenspray Dermapharm®
- Panthenol Meerwasser Nasenspray JENAPHARM®
Catalogue references include BZ00178, TD_Moisturising Lozenges, VA00433, VD10294, VE00049, VE00938.
European nomenclature codes declared: Q030103, A030499, Z12040299, V9099, V9017.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| 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 | 8 |
|---|---|
| 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. Anton Hübner GmbH & Co. KG was not found in either the U.S. or the Canadian register.