Knop Elektronik A/S
DK-MF-000025631 · Denmark · Struer
Knop Elektronik A/S is registered in the European database on medical devices as a manufacturer, with 33 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 33 |
|---|
Most frequent device types declared: CT901, KK901, LAK901, MR902, PIR900.
Among these devices, 32 are declared active.
Devices declared under this manufacturer
- CT901BED
- KK100
- KK901P
- LAK901
- MR902
- PIR900
- POS901
- POS901S
- PU101
- PU901
- PU901P
- TX901
Showing 12 of 33 declared devices.
Catalogue references include EPI900, KK100, KK901AP, LAK901, PIR900, PU901P.
European nomenclature codes declared: Y214299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 33 |
| 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 | 33 |
|---|---|
| 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. Knop Elektronik A/S was not found in either the U.S. or the Canadian register.