NanoRepro AG
DE-MF-000023735 · Germany · Marburg
NanoRepro AG is registered in the European database on medical devices as a manufacturer, with 50 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Among these devices, 1 are declared sterile.
Devices declared under this manufacturer
- CeliacDetect
- Co-TEST KELIAKIATESTI
- DR. VIVIEN KARL Vaginalpilz-Schnelltest
- FerritinCHECK
- FertiQUICK
- GlutenCHECK
- GlutenCHECK [TR/EN]
- RapiChek CandidaTEST
- RapiChek FerritinTEST
- Screen Test Celiachia
- VagiQUICK
- Veroval ZELFTEST IJzertekort
Showing 12 of 50 declared devices.
Catalogue references include 360610, 400600, 400620, 400650, 400660, 500250.
European nomenclature codes declared: W01021699, W0102160399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 50 |
| 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. NanoRepro AG was not found in either the U.S. or the Canadian register.