avateramedical GmbH
DE-MF-000019824 · Germany · Jena
avateramedical GmbH is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|---|
| Class IIb | 3 |
Among these devices, 7 are declared sterile, 1 active.
Devices declared under this manufacturer
- Atraumatische Greifzange
- Maryland Dissektor
- Metzenbaum Schere
- Nadelhalter
- Set Sterilabdeckung
- Sterilhülle Endoskop 0°
- Sterilhülle Endoskop 30°
- avatera Telemanipulator
Catalogue references include 11000000002, 11401000006, 11404000001, 11405000001, 11501000005, 11502000005.
European nomenclature codes declared: Z12020185, T030299, Z12020101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. avateramedical GmbH was not found in either the U.S. or the Canadian register.