PlantTec Medical GmbH
DE-MF-000005921 · Germany · Lüneburg
PlantTec Medical GmbH is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 4 |
|---|---|
| Class IIa | 2 |
Among these devices, 6 are declared sterile, 4 implantable.
Devices declared under this manufacturer
- 4DFLap™
- 4DryField® PH
Catalogue references include LA0014-EU, LA0038-EU, SK0001-EU, SK0003-EU, SK0005-EU, SK0009-EU.
European nomenclature codes declared: M040599,M0406, A99.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 6 |
|---|---|
| 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. PlantTec Medical GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
7272GB448250701 | issued | 2029-10-09 |
13370GB450250701 | issued | 2030-06-30 |