Nordema GmbH
DE-MF-000008684 · Germany · Geestland
Nordema GmbH is registered in the European database on medical devices as a manufacturer, with 37 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 37 |
|---|
Among these devices, 24 are declared implantable.
Devices declared under this manufacturer
- KENTFIL+
- LUMIFIL+
- Nordema Bite Reg
- Nordema Bracket Bond
- Nordema Clean & Polish Paste
- Nordema GIC Filling Plus
- Nordema LC Desensitizer
- Nordema Nano Hybrid Composite Disc
- Nordema Print IBT
- Nordema Retraction Paste
- Nordema SC Soft Relining - cartridge
- Nordema SC Temp C&B Material - 50 ml cartridge
Showing 12 of 37 declared devices.
Catalogue references include 3134951, 3134952, 3134953, 3134957, 7198, 8535.
European nomenclature codes declared: Q010199, Q01020605, Q01010199, Q010699, Q0101010299, Q010499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 37 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. Nordema GmbH was not found in either the U.S. or the Canadian register.