AIDA GmbH
DE-MF-000040784 · Germany · Bad Kreuznach
AIDA GmbH is registered in the European database on medical devices as a manufacturer, with 34 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- CenpB
- DANA-Pro
- ENA Screen
- Histon-H1
- Histon-H2B
- Histon-H4
- Jo-1
- PD DETECT II
- PM-Scl
- RNP complex
- Scl-70
- U1-70
Showing 12 of 34 declared devices.
Catalogue references include 10102, 10104, 10105, 10113, 10116, 10140.
European nomenclature codes declared: W0102100107, W01019099, W0102100101, W0102100106, W0102100105, W0102100114.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 34 |
| 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 | 34 |
|---|---|
| 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. AIDA GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
HX 2699595-1 | issued | 2031-02-08 |