Camp Scandinavia AB
SE-MF-000021395 · Sweden · Helsingborg
Camp Scandinavia AB is registered in the European database on medical devices as a manufacturer, with 1 922 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 1 922 |
|---|
Devices declared under this manufacturer
- ACTIVE X KNEE SHORT WRAP
- ACTIVE X KNEE SLEEVE 1 SPIRAL STAY
- BLUEROCKER 2.0 W D-RING W COMFORTKIT
- BLUEROCKER 2.0 W/O D-RING W SOFTKIT
- BLUEROCKER 2½ W/O D-RING W SOFTKIT
- KIDDIEROCKER W/O D-RING
- KIDDIEROCKER W/O D-RING 1 PC COMFORTKIT
- SELECTION MULTI OPEN
- SELECTION WRIST ORTHOSIS SOFT
- STRAPS TOEOFF w VELCRO
- TOEOFF 2½ W D-RING
- TOEOFF 2½ W D-RING W MOUNTED COMFORTKIT
Showing 12 of 1 922 declared devices.
Catalogue references include 280510015, 288840012, 289021012, 289601013, 389402014, 389451010.
European nomenclature codes declared: Y06120602, Y060612, Y06120601, Y061280, Y061209, Y060603.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | CAMP SCANDINAVIA AB (SE) · FDA 8030901 |
| Devices in EUDAMED | 1 922 |
| Country of registration | Sweden |
Device-level evidence
| Devices with a numeric GTIN | 1 922 |
|---|---|
| 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: United States only. Camp Scandinavia AB is registered in the United States but was not found in the Canadian register.