Microwarm ApS
DK-MF-000017837 · Denmark · Kgs. Lyngby
Microwarm ApS is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 7 |
|---|
Most frequent device types declared: Decuheel.
Devices declared under this manufacturer
- Curapax® Classic Professional
- Curapax® Mini Classic Professional
- DecuLeg
- Decuheel
Catalogue references include 05711265153022, 5711265150113, 5711265153046, Curapax® Classic Professional, Curapax® Mini Classic Professional, DecuLeg.
European nomenclature codes declared: V08030102, M9001, V080399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| Country of registration | Denmark |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 7 |
|---|---|
| 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. Microwarm ApS was not found in either the U.S. or the Canadian register.