Reimers & Janssen GmbH
DE-MF-000032145 · Germany · Waldkirch
Reimers & Janssen GmbH is registered in the European database on medical devices as a manufacturer, with 21 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 21 |
|---|
Most frequent device types declared: 172.
Among these devices, 13 are declared active.
Devices declared under this manufacturer
- Aku-Wave 4
- Cluster probe
- LaserPen Expert
- LaserPen M
- LaserPen Praxis
- LaserPen Standard
- Laserpen Expert
- LightNeedle
- LightNeedle mini
- LightStream Base Station
- LightStream HighPower
- Physiolaser olympic
Showing 12 of 21 declared devices.
Catalogue references include 132, 134A, 139, 172, 174, 300.
European nomenclature codes declared: Z120615.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 21 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 21 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | REIMERS & JANSSEN GMBH |
North American profile: Canada only. Reimers & Janssen GmbH holds a Canadian licence but was not found in the U.S. register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
7281GB448240412 | issued | 2028-10-11 |