Protac A/S
DK-MF-000000963 · Denmark · Skanderborg
Protac A/S is registered in the European database on medical devices as a manufacturer, with 244 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 244 |
|---|
Devices declared under this manufacturer
- Protac Ball Blanket Calm
- Protac Ball Blanket Combi
- Protac Ball Blanket Flexible
- Protac Granulate Blanket Flexible
- Protac Kugledynen Calm
- Protac Kugledynen Flexible Junior
- Protac Kugledynen Granulat
- Protac Kuglepuden
- Protac MyFit
- Protac MyFit Easy
- Protac SenSit
- Protac SenSit Nature
Showing 12 of 244 declared devices.
Catalogue references include 100-215-V-220-85, 100-401-V-220-85, 600-702-3820-41, 600-712-3000-42, 800-821-10-M/L, 800-841-10-XL/2XL.
European nomenclature codes declared: Y99.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 244 |
| 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 | 244 |
|---|---|
| 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. Protac A/S was not found in either the U.S. or the Canadian register.