Greiner GmbH
DE-MF-000007660 · Germany · Pleidelsheim
Greiner GmbH is registered in the European database on medical devices as a manufacturer, with 203 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 203 |
|---|
Most frequent device types declared: 21, 220, 422, 424, 426.
Among these devices, 168 are declared active.
Devices declared under this manufacturer
- ATMOS Chair Professional
- Behandlungsstuhl
- Blutabnahme- Patientenstuhl Serie 22
- CARELINE MAN,AH
- Carryline Cross
- Carryline Mobil
- MULTILINE NEXT DC
- Medseat
- Multiline Next IT
- Multiline next
- Relax
- Stuhl 210 UT76 SA
Showing 12 of 203 declared devices.
Catalogue references include 2207340, 4224000, 4225200, 426, 4460131, 4616600.
European nomenclature codes declared: V08020101, V080202, V080502, V08020101,V080202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 203 |
| 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 | 203 |
|---|---|
| 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. Greiner GmbH was not found in either the U.S. or the Canadian register.