mediPlac GmbH
DE-MF-000008087 · Germany · Borchen
mediPlac GmbH is registered in the European database on medical devices as a manufacturer, with 288 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 288 |
|---|
Most frequent device types declared: Lagerungshilfen zur Druckentlastung.
Among these devices, 288 are declared reusable.
Catalogue references include 300.719, 300.751, 800.004-316A-2, 800.004-4034-2, 800.031-K, 800.121-E-4054-1.
European nomenclature codes declared: V08030102, V080302, V0804, Z12011299, Z12011280, V0880.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 288 |
| 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 | 288 |
|---|---|
| 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. mediPlac GmbH was not found in either the U.S. or the Canadian register.