CoMoveIT
BE-MF-000017867 · Belgium · Assebroek
CoMoveIT is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 15 |
|---|
Among these devices, 15 are declared active.
Devices declared under this manufacturer
- CoMoveIT Drive
- CoMoveIT Drive rod set
- CoMoveIT Flex
- CoMoveIT Flex Foot
- CoMoveIT Flex dF
- CoMoveIT Smart ECU
- CoMoveIT Smart F
- CoMoveIT Smart H3
- CoMoveIT Smart dF
- ECU Mounting Plate Ottobock
- ECU Mounting Plate Permobil
- Headset Mounting Clamp
Showing 12 of 15 declared devices.
Catalogue references include 05430002911144, 05430002911151, 05430002911168, CM0001, CoMoveIT Flex, CoMoveIT Flex Footpad.
European nomenclature codes declared: Y122403.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 15 |
| Country of registration | Belgium |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 15 |
|---|---|
| Found in the U.S. device database | 7 |
| Share | 46.7 % |
⚠ The two levels disagree here. This company’s name was not found in the FDA establishment register, yet some of its devices are in the U.S. device database. The likeliest reading is that the name match failed.
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. CoMoveIT was not found in either the U.S. or the Canadian register.