AMO Uppsala AB
SE-MF-000017467 · Sweden · Uppsala
AMO Uppsala AB is registered in the European database on medical devices as a manufacturer, with 46 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 45 |
|---|---|
| Class I | 1 |
Most frequent device types declared: 10271012, 10271014, 10271514, 10272011, 10272012.
Among these devices, 46 are declared sterile, 44 implantable.
Devices declared under this manufacturer
- HEALON DUET PRO II
- HEALON ENDOCOAT PRO
Showing 12 of 46 declared devices.
Catalogue references include 10271014, 10271514, 10272011, 10272012, 10292011, 10292014.
European nomenclature codes declared: Q02030301.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | AMO UPPSALA AB (SE) · FDA 3004750704 |
| Devices in EUDAMED | 46 |
| Country of registration | Sweden |
Device-level evidence
| Devices with a numeric GTIN | 2 |
|---|---|
| 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. AMO Uppsala AB is registered in the United States but was not found in the Canadian register.