Dr. August Wolff GmbH & Co. KG Arzneimittel
DE-MF-000005943 · Germany · Bielefeld
Dr. August Wolff GmbH & Co. KG Arzneimittel is registered in the European database on medical devices as a manufacturer, with 24 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 24 |
|---|
Devices declared under this manufacturer
- Gleitgelen Lipogeel
- V-san IdroCrema
- V-san Vlažilna krema
- V-san vlažilni Cremolum
- Vagisan Acid lactic
- Vagisan Cremolum globulki nawilżające
- Vagisan FeuchtCreme
- Vagisan FeuchtCreme Cremolum
- Vagisan Hüvelyhidratáló krém
- Vagisan Milchsäure
- Vagisan Pflegendes Gleitgel
- Vagisan kosteuttava emätinvoide kombi
Showing 12 of 24 declared devices.
Catalogue references include 00019230, 00019745, 00023834, 00062211, 00066936, 00066996.
European nomenclature codes declared: U0803.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 24 |
| 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 | 24 |
|---|---|
| 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. Dr. August Wolff GmbH & Co. KG Arzneimittel was not found in either the U.S. or the Canadian register.