Weyer GmbH
DE-MF-000029826 · Germany · Kürten
Weyer GmbH is registered in the European database on medical devices as a manufacturer, with 19 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 13 |
|---|---|
| Class IIb | 6 |
Most frequent device types declared: WY1480, WY1481, WY1482, WY2016, WY2401.
Among these devices, 17 are declared active, 13 with a measuring function.
Devices declared under this manufacturer
- BILICOMPACT® LED
- CERAMOTHERM 3100
- CERAMOTHERM 3200
- CERAMOTHERM 3300
- REANIMAT O2 Blend
- THERMOCARE C
- THERMOCARE K
- THERMOCARE KCE
- THERMOCARE Vita
- THERMOCARWE Vita Vario
- VARIOTERM C
- VARIOTHERM C
Showing 12 of 19 declared devices.
Catalogue references include WY1480, WY1481, WY1482, WY2016, WY2401, WY3004.
European nomenclature codes declared: Z12080405, Z120309, Z1208040302, Z12080407, Z12080401, Z12080404.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 19 |
| 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 | 19 |
|---|---|
| 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. Weyer GmbH was not found in either the U.S. or the Canadian register.