Catell AB
SE-MF-000000726 · Sweden · Älta
Catell AB is registered in the European database on medical devices as a manufacturer, with 689 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 689 |
|---|
Devices declared under this manufacturer
- Base Comfort Black, L S
- Base Frank Black, R XL
- Base Max Beige L S
- Base Max Strong Black, R XXL
- Catell Tape, Light Blue, 5 cm x 5 m, 24 pcs/pkg
- Catell Wrap, 2,5 cm x 4,5 m Beige, 24 pcs/pkg
- EDEMA Light Long, Fullfinger, M, Beige
- EDEMA Light Thumb, L, Beige
- Easy Comfort Black, L XL
- Ella Soft, Black, Left XS
- Finger More, Black, XS, Pack size 30
- Lacy Short Stabil Black R M
Showing 12 of 689 declared devices.
Catalogue references include 3050-24, 7080-23, 7350-4, 7706-33, 7707-35, 7715-02.
European nomenclature codes declared: Y060606, M030499, Y060613, M0304010301, Y060630, H900299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 689 |
| 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 | 689 |
|---|---|
| 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. Catell AB was not found in either the U.S. or the Canadian register.