Bayer Consumer Care AG
CH-MF-000014141 · Switzerland · Basel
Bayer Consumer Care AG is registered in the European database on medical devices as a manufacturer, with 37 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 35 |
|---|---|
| Class IIa | 2 |
Most frequent device types declared: Bepanthen Itch Relief.
Authorised representative in the Union: Bayer Vital GmbH.
Devices declared under this manufacturer
- Bepanderm®
- Bepanthen Sensiderm Anti-Juckreiz Creme
- Bepanthen Sensiderm Cream
- BepanthenSensicalm® Paupières
- Bepanthene® Cooling Foam Spray
- Bepanthene® Eczema
- Bepanthenol® Sensiderm Crema
- Bepanthen® Eczeem Crème Baby
- Bepanthen® Kuehlendes Schaumspray
- Bepanthen® Sensiderm Anti-Juckreiz Creme
- Bepanthen® Sensiderm Cremă
- Bepanthen® Sensiderm Krem
Showing 12 of 37 declared devices.
Catalogue references include 04064273000248, 04064273110008, 04064273120069, 04064273120083, 04064273130075, 04064273150004.
European nomenclature codes declared: M04041503, M0408, M0410, V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 37 |
| Country of registration | Switzerland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 36 |
|---|---|
| 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. Bayer Consumer Care AG was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G70 054972 0039 | issued | 2030-03-24 |
G70 054972 0038 | issued | 2030-02-17 |