Glaswarenfabrik Karl Hecht GmbH & Co KG
DE-MF-000006553 · Germany · Sondheim/Rhön
Glaswarenfabrik Karl Hecht GmbH & Co KG is registered in the European database on medical devices as a manufacturer, with 68 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 47 |
|---|
Most frequent device types declared: 40440, 41024, 42885, 43017, 44302.
Among these devices, 34 are declared reusable.
Catalogue references include 40440701, 40440703, 40444702, 40445702, 42886004, 42892001.
European nomenclature codes declared: L059001, W02020199, G06, A1101, V9001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 68 |
| 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 | 68 |
|---|---|
| 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. Glaswarenfabrik Karl Hecht GmbH & Co KG was not found in either the U.S. or the Canadian register.