Krucom AB
SE-MF-000047914 · Sweden · Lund
Krucom AB 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 |
|---|
Most frequent device types declared: X-Tray.
Devices declared under this manufacturer
- X-Tray 3.20.0
- X-Tray 3.21.0
- X-Tray 3.22.0
- X-Tray 3.22.1
- X-Tray 3.23.0
- X-Tray 3.24.0
- X-Tray 3.25.0
- X-Tray 3.25.1
- X-Tray 3.25.2
Catalogue references include 3.20.0, 3.21.0, 3.22.1, 3.23.0, 3.24.0, 3.25.0.
European nomenclature codes declared: Z119082.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | Sweden |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| 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. Krucom AB was not found in either the U.S. or the Canadian register.