Moeck & Moeck GmbH
DE-MF-000007979 · Germany · Hamburg
Moeck & Moeck GmbH is registered in the European database on medical devices as a manufacturer, with 39 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 29 |
|---|---|
| Class IIb | 10 |
Most frequent device types declared: TWINWARM BB, Twinwarm BB 12BB01 (deutsch), Twinwarm BB 12BB02 (italiano), Twinwarm BB 12BB05 (english), Twinwarm BB 12BB06 (français).
Among these devices, 10 are declared active.
Devices declared under this manufacturer
- 12BB-DE-EF
- 12BB-EN-EF
- 12BB-FR-EF
- 12BB-IT-EF
- 12BB-SV-EF
- 895 (GKD) Ganzkörperdecke
- 904 (EW II) Erwachsenen II
- 906 (UNI II) Universal II
- 906 UNI II
- 908 Multi I
- 910 (UNI III) Universal III
- Twinwarm BB 12BB02
Showing 12 of 39 declared devices.
Catalogue references include 11WD895MM, 11WD904MS02, 11WD906MS04, 11WD906MS05, 11WD906MS06, 11WD906MS08.
European nomenclature codes declared: T030301, V9099, T030301,V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 39 |
| 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 | 39 |
|---|---|
| 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. Moeck & Moeck GmbH was not found in either the U.S. or the Canadian register.