Cerascreen GmbH
DE-MF-000017602 · Germany · Schwerin
Cerascreen GmbH is registered in the European database on medical devices as a manufacturer, with 192 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- DNA Hautgesundheits Test
- cerascreen® COVID-19 Vaccine Effectiveness Test
- cerascreen® CholesterinTest
- cerascreen® Genetic Age Test
- cerascreen® Lebensmittel-Reaktionstest
- cerascreen® Milch und Ei Allergie-Test
- cerascreen® Milk + Egg Allergy Test
- cerascreen® Omega-3 Test
- cerascreen® Pollen Allergy Test
- cerascreen® Thyroid Test
- cerascreen® Vitamin B12 Test
- cerascreen® hsCRP Test
Showing 12 of 192 declared devices.
Catalogue references include 99010032, 99010058, 99010155, 99010286-D, 99010445, 99010486.
European nomenclature codes declared: W0501010201, W05019099, W05019001, W05019002, W05010202, W0501010201,W05019002.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 192 |
| 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 | 192 |
|---|---|
| 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. Cerascreen GmbH was not found in either the U.S. or the Canadian register.