M. G. Kurth GmbH
DE-MF-000045501 · Germany · Schwarzenbek
M. G. Kurth GmbH is registered in the European database on medical devices as a manufacturer, with 100 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 100 |
|---|
Most frequent device types declared: Bite Covers, ScanSleeves Standard Line.
Devices declared under this manufacturer
- Anmischblock - Klotz
- Anmischblock Antirutschbeschichtung
- Anmischblock, Antirutschbeschichtung
- Anmischblock, mittel
- Folienblock Antirutschbeschichtung
- Folienblock, Antirutschbeschichtung
- Hygiene-Schutzhüllen
- Hygiene-Schutzhüllen für Aufbiss
- POLY Mixing Pad
- Pergament Anmischblock, mittel
- Pergament Anmischblock, universal
- Speicherfolien-Schutzhülle Plus-Line
Showing 12 of 100 declared devices.
Catalogue references include 70102A, 70132, 70303, 70403, 80802, 80931.
European nomenclature codes declared: Q010503, T030102, T030402.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 100 |
| 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. M. G. Kurth GmbH was not found in either the U.S. or the Canadian register.