Konmex Spółka z ograniczoną odpowiedzialnością
PL-MF-000033845 · Poland · Warsaw
Konmex Spółka z ograniczoną odpowiedzialnością is registered in the European database on medical devices as a manufacturer, with 18 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 18 |
|---|
Most frequent device types declared: LAP5 Disposable Endoscopic Instruments.
Among these devices, 18 are declared sterile, 18 active.
Devices declared under this manufacturer
- LAP 5 Disposable Endoscopic Atraumatic Fenestrated Grasper
- LAP 5 Disposable Endoscopic Dissector Maryland
- LAP 5 Disposable Endoscopic Grasper Allis
- LAP 5 Disposable Endoscopic Grasper Babcock
- LAP 5 Disposable Endoscopic Grasper Maxi Grip
- LAP 5 Disposable Endoscopic Hook Scissors
- LAP 5 Disposable Endoscopic Metzenbaum Scissors
- LAP 5 Disposable Endoscopic Straight Scissors
- LAP 5 Disposable Endoscopic Toothed Grasper
Showing 12 of 18 declared devices.
Catalogue references include 0208-DDLAP501, 0208-DGLAP501, 0208-DGLAP501B, 0208-DGLAP504, 0208-DGLAP504B, 0208-DSLAP501B.
European nomenclature codes declared: K0201010602, K0201010402, K0201010202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 18 |
| Country of registration | Poland |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 18 |
|---|---|
| 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. Konmex Spółka z ograniczoną odpowiedzialnością was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
1434-MDR-003/2024 | issued | 2029-04-18 |