KD Medical GmbH Hospital Products
DE-MF-000006773 · Germany · Berlin
KD Medical GmbH Hospital Products is registered in the European database on medical devices as a manufacturer, with 687 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 687 |
|---|
Among these devices, 687 are declared sterile, 41 with a measuring function.
Devices declared under this manufacturer
- KD-FINE
- KD-FINE BLUNT
- KD-FINE SAFETY
- KD-FIX
- KD-FIX +
- KD-FIX SOLO
- KD-FIX-MONO SAFETY
- KD-FIX-SAFETY
- KD-FIX-SAFETY +
- KD-FIX-SAFETY PRO
- KD-FIX-SOLO SAFETY
- KD-FLY SAFETY
Showing 12 of 687 declared devices.
Catalogue references include 767030A, 777565M, 870860, 911631S, 911693S, 912393E.
European nomenclature codes declared: A0101010101, C0101010102, A01010201, A01010202, A0101010102, C0101010202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 687 |
| 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 | 411 |
|---|---|
| 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. KD Medical GmbH Hospital Products was not found in either the U.S. or the Canadian register.