Hans Dinslage GmbH
DE-MF-000005488 · Germany · Uttenweiler
Hans Dinslage GmbH is registered in the European database on medical devices as a manufacturer, with 136 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 136 |
|---|
Most frequent device types declared: SBM 15, SBM 18, SBR 55, SEM 46, SEMEL 50100.
Among these devices, 135 are declared active, 38 with a measuring function.
Catalogue references include 85862, 85927, 86084, 86086, 86130, 86297.
European nomenclature codes declared: Z129099, Y2145060101, R060101, Z1203020408, Z120601, Z120607.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 136 |
| 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 | 136 |
|---|---|
| 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. Hans Dinslage GmbH was not found in either the U.S. or the Canadian register.