Careva System AB
SE-MF-000004861 · Sweden · Göteborg
Careva System AB is registered in the European database on medical devices as a manufacturer, with 40 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 40 |
|---|
Most frequent device types declared: Careva Systems, Crossit.
Devices declared under this manufacturer
- Buckle Extra long
- Chest Buckle
- Chest belt
- Chest belt L
- Chest belt M
- Combi belt L
- Combi belt S
- Hip (pelvic) KIT
- Hip (pelvic) belt L
- Hip (pelvic) belt M
- Shoulder KIT
- Shoulder belt M
Showing 12 of 40 declared devices.
Catalogue references include 10023 S, 10030 m, 10080, 10100, 10135 XL, 10285 M, L.
European nomenclature codes declared: Y180980.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 40 |
| 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 | 40 |
|---|---|
| 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. Careva System AB was not found in either the U.S. or the Canadian register.