MIM Pharma Europe AB
SE-MF-000048118 · Sweden · Fengersfors
MIM Pharma Europe AB is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Most frequent device types declared: KS015, MIM-ALL-NS-001, SinaVita-MIG-INHAL-01.
Among these devices, 1 are declared active.
Devices declared under this manufacturer
- SinaVita® Allergy Support Inhalation Drops
- SinaVita® Allergy Support Nasal Spray
- SinaVita® Immune Support Inhalation Drops
- SinaVita® Immune Support Nasal Spray
- SinaVita® Immune Support Oral Spray
- SinaVita® Migraine Support Inhalation Drops
- SinaVita® Migraine Support Nasal Spray
- SinaVita® Respiratory Support Inhalation Drops
- SinaVita® Respiratory Support Nasal Spray
- SinaVita® Respiratory Support Oral Spray
Catalogue references include MIM-ALL-NS-001, MIM-IMM-NS-001, MIM-IMM-OS-001, MIM-RESP-ID-001, MIM-RESP-NS-001, MIM-RESP-OS-001.
European nomenclature codes declared: Q030103, R060203, R0699.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| 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 | 11 |
|---|---|
| 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. MIM Pharma Europe AB was not found in either the U.S. or the Canadian register.