modul technik GmbH
DE-MF-000014647 · Germany · Montabaur
modul technik GmbH is registered in the European database on medical devices as a manufacturer, with 31 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 31 |
|---|
Most frequent device types declared: Medizinische Versorgungseinheit, Medizinische Versorgungseinheiten, Typenreihe modulux.
Among these devices, 31 are declared active.
Devices declared under this manufacturer
- DVE 5500-D
- IME 1500
- IME duplex
- IVV 1054 UP
- MEV junior
- VIP 2000
- ambient compact
- ambient cube
- ambient junior
- ambient light
- moduflex nova
- moduversa HM plus
Showing 12 of 31 declared devices.
Catalogue references include IME duplex, IVV 1054 UP, VIP 2000, ambient compact, ambient cube, moduflex nova.
European nomenclature codes declared: Z120309.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 31 |
| 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 | 31 |
|---|---|
| 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. modul technik GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
44911222228 | issued | 2030-12-02 |