Erimed International AB
SE-MF-000032221 · Sweden · SKÄRHOLMEN
Erimed International AB is registered in the European database on medical devices as a manufacturer, with 80 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 80 |
|---|
Devices declared under this manufacturer
- CRUZ MAN DARK BROWN D 45
- CRUZ WOMAN BLACK D 37
- CRUZ WOMAN BLACK D 40
- CRUZ WOMAN TAUPE D 40
- DELPHI 4 Woman Black D 37
- DELPHI 4 Woman Black D 38
- DICTUS DS-02J CHILD BLACK
- DICTUS DS-02J CHILD NATUR
- DICTUS IN DS-03 BLACK LEFT
- DICTUS IN DS-03J CHILD NATUR
- ESPIRIT 4 Woman Black D 39
- ESPIRIT 4 Woman Black D 41
Showing 12 of 80 declared devices.
Catalogue references include 530200-000, 530201-000, 530300-111, 863112-038, 863212-037, 863212-040.
European nomenclature codes declared: Y063303, Y06120602, Y061218, Y061216.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 80 |
| 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 | 80 |
|---|---|
| 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. Erimed International AB was not found in either the U.S. or the Canadian register.