Albert Heiss GmbH & Co. KG
DE-MF-000005495 · Germany · Tuttlingen
Albert Heiss GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 1 181 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 1 181 |
|---|
Most frequent device types declared: Eye Speculum, Forceps, Hook, Knife, Marker.
Among these devices, 912 are declared reusable.
Catalogue references include H-1743, H-2561/13, H-2636/4, H-2812/4, H-3357DA, H-4250.
European nomenclature codes declared: L170201, L170102, L1711, L01040501, L1713, L1706.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 1 181 |
| 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 | 1 181 |
|---|---|
| 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. Albert Heiss GmbH & Co. KG was not found in either the U.S. or the Canadian register.