Queisser Pharma GmbH & Co. KG
DE-MF-000005291 · Germany · Flensburg
Queisser Pharma 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 |
|---|
Devices declared under this manufacturer
- Protefix Haft-Creme Classic
- Protefix Haft-Creme Minze
- Protefix Haft-Creme Neutral
- Protefix Haft-Creme Premium
- Protefix Haft-Creme mit Aloe Vera
- Protefix Haft-Polster Oberkiefer
- Protefix Haft-Polster Unterkiefer
- Protefix Haft-Pulver
- Protefix Wund- und Schutzgel
Catalogue references include 04009932002102, 04009932002133, 04009932002164, 04009932002171, 04009932002201, 04009932003109.
European nomenclature codes declared: Q010299, V9099.
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.
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. Queisser Pharma GmbH & Co. KG was not found in either the U.S. or the Canadian register.