Remy & Geiser GmbH
DE-MF-000020726 · Germany · Schleusingen
Remy & Geiser GmbH is registered in the European database on medical devices as a manufacturer, with 715 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 715 |
|---|
Catalogue references include 10986-AR2400001, 11254-AR240001, 11467-AR850001, 12176_V02-AR850001, 4240M-AR240001, 9208M-AR240001.
European nomenclature codes declared: A99, A13.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 715 |
| 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 | 715 |
|---|---|
| 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. Remy & Geiser GmbH was not found in either the U.S. or the Canadian register.