Kanmed AB
SE-MF-000001839 · Sweden · Sollentuna
Kanmed AB is registered in the European database on medical devices as a manufacturer, with 72 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 72 |
|---|
Among these devices, 16 are declared active.
Devices declared under this manufacturer
- Embrace Base Plate Atom V-808
- Embrace Base Plate Dräger TI 500
- Kanmed BabyBed Twin fixed height, w/o rails
- Kanmed BabyBed Without rail, Twin
- Kanmed Babybed Standard
- Kanmed Blanket Warming Cabinet Large - 120 V version
- Kanmed Blanket Warming Cabinet Small - 120 V version
- Kanmed Combination Warming Cabinet
- Kanmed Tent BabyBed twin
- Kanmed Tent BabyBed, Blue/Yellow
- Kanmed Universal Warming Cabinet Dual Access Large - 120 V version
- Kanmed Universal Warming Cabinet Large - 120 V version
Showing 12 of 72 declared devices.
Catalogue references include BB100, BB162, BB401F, GE-2350D, GE-2350L-120, GE2380S-120.
European nomenclature codes declared: A030105, Z12040208, V08068099, V0804, V0201, V0806010701.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 72 |
| 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 | 72 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | KANMED AB |
North American profile: Canada only. Kanmed AB holds a Canadian licence but was not found in the U.S. register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
28620221903 | issued | 2030-06-09 |