HERRMANN Apparatebau GmbH
DE-MF-000006133 · Germany · Elsenfeld
HERRMANN Apparatebau GmbH is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 16 |
|---|---|
| Class IIb | 4 |
Most frequent device types declared: CHT-Spekula Set, Colon Hydromat, Hyper Medozon comfort.
Among these devices, 14 are declared active.
Devices declared under this manufacturer
- CHT Spekula L 1,20m
- CHT Spekula L 1,50m
- CHT Spekula M 1,20m
- CHT Spekula M 1,50m
- CHT Spekula Set S 1,20m
- CHT Spekula Set S 1,50m
- Colon Hydromat comfort
- Colon Hydromat standard
- Hyper Medozon comfort grün
- Hyper Medzon comfort silber
- Medozon compact grün
- Medozon compact silber
Showing 12 of 20 declared devices.
Catalogue references include 15571, 15580, 15582, 15583, 15584, 16801.
European nomenclature codes declared: Z120499, G020301, Z12040207.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 20 |
| 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 | 20 |
|---|---|
| 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. HERRMANN Apparatebau GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G10 051287 0016 | supplemented | 2027-12-05 |