Schlumbohm GmbH & Co. KG
DE-MF-000005266 · Germany · Brokstedt
Schlumbohm GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 6 |
|---|
Most frequent device types declared: KnochenFilter KF-T3, Knochenmühle.
Among these devices, 3 are declared reusable, 3 active.
Devices declared under this manufacturer
- EndoPilot comfort
- KF-T3
- Knochenmühle KM-3
Catalogue references include 104 3100, 108 0030, 110 0101.
European nomenclature codes declared: Q010399, Q010199, P01020180.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | SCHLUMBOHM GMBH & CO. KG (DE) · FDA 3018783058 |
| Devices in EUDAMED | 6 |
| Country of registration | Germany |
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 | Licensed in Canada |
|---|---|
| Matched entry | SCHLUMBOHM GMBH & CO. KG |
North American profile: Both markets. Schlumbohm GmbH & Co. KG is registered in both the United States and Canada.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
1712GB448250912 | issued | 2030-04-08 |