Paul Marienfeld GmbH & Co. KG
DE-MF-000023724 · Germany · Lauda-Königshofen
Paul Marienfeld GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 995 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Devices declared under this manufacturer
- DG 10x12,5 N.1 V=100 STÜ Superiorerior
- DG 12,8 D N.3 V=50 STÜ Superior CE
- DG 24x40 N.5 V=25 SDD Superior CE
- DG 47 D N.1,5H silik V=100 Papp Superior CE
- DG 75,5x111,5 N.1,5H V=50 Papp Superior CE
- DG 75x100 N.1,5 Papzw. V=50 Papp Superior CE
- DG 95x100 N.1 V=100 Papzw Papp Superior CE
- Histob+ S Float weiß V=100 Plasch Superior
- OT 10F 7mm blau V=50 Superior
- OT 24F 4mm grün MR 15 V=50 Superior
- OT 2F 11mm blau V=50 Superior
- OT 76,2x25,2x1 Float fbk oMR V=50 Superior CE
Showing 12 of 995 declared devices.
Catalogue references include 010199909109, 0106992096, 0114990092, 0704107, 0810501, 1215671.
European nomenclature codes declared: W0503900202, W0503900201, W02020199.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | PAUL MARIENFELD GMBH & CO. KG. (DE) · FDA 8010388 |
| Devices in EUDAMED | 995 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 995 |
|---|---|
| Found in the U.S. device database | 963 |
| Share | 96.8 % |
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: United States only. Paul Marienfeld GmbH & Co. KG is registered in the United States but was not found in the Canadian register.