Likamed GmbH
DE-MF-000006475 · Germany · Eppingen
Likamed GmbH is registered in the European database on medical devices as a manufacturer, with 18 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 18 |
|---|
Most frequent device types declared: 59-00-00, Mechanical therapy chair, Shockwave therapy device, Therapy bed chair, Therapy chair.
Among these devices, 15 are declared active, 1 with a measuring function.
Devices declared under this manufacturer
- ComfortLine3
- LiKAWAVE VARIO® 3i
- SALSA® A1
- SALSA® A3
- SALSA® A4
- SALVA®
- SALVA® plus
- SEMA®
- SENSA i scale
- SENSA® Flex A3
- SENSA® Flex A4
- SENSA® i
Showing 12 of 18 declared devices.
Catalogue references include 57-A1-00, 58-00-00, 59-00-00, 61-C5-01, 61-F3-00, 61-I-00.
European nomenclature codes declared: V08020101, Z12139001, V080502, V08060199,Z12099003, V080202, Z12099003.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | LIKAMED GMBH (DE) · FDA 3000335752 |
| Devices in EUDAMED | 18 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 18 |
|---|---|
| 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: United States only. Likamed GmbH is registered in the United States but was not found in the Canadian register.