INTERCUS GmbH
DE-MF-000005084 · Germany · Bad Blankenburg
INTERCUS GmbH is registered in the European database on medical devices as a manufacturer, with 87 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 87 |
|---|
Devices declared under this manufacturer
- Bohrdrahtlehre, für Drähte D 1,0 mm - D 2,5 mm
- GN Explantationsset
- GNp T-Griff modular
- Lagerungssieb, für Femurplatten, distal, lateral, polyaxial
- Lagerungssieb, für Femurplatten, proximal, polyaxial winkelstabil, ein
- Lagerungssieb, für Großfragmentplatten System, winkelstabil, komplett,
- Lagerungssieb, für Großfragmentschrauben (Tibia) D 4,5 mm - D 5,5 mm,
- Lagerungssieb, für Handsystem INCUS-Schrauben, Kunststoff, komplett
- Lagerungssieb, für NAVICUS-Fußplatten, für Schrauben D 2,2 mm, Kunstst
- Lagerungssieb, für Schrauben D 2,5 mm/D 3,0 mm
- Lagerungssieb, für distales Tibia-/Fibulaplatten System, polyaxial win
- Lagerungssieb, für durchbohrte Schrauben D 4,0 mm, Kunststoff, komplet
Showing 12 of 87 declared devices.
Catalogue references include 1133151, 1133320, 750.105201, 750.108038, 750.108059, 750.108066.
European nomenclature codes declared: V0480, L99, L0903, L091099, L0922, L0317.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 87 |
| 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 | 87 |
|---|---|
| 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. INTERCUS GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
HZ 1284600-1 | issued | 2031-08-02 |