Synformulas GmbH
DE-MF-000016381 · Germany · Gräfelfing
Synformulas 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 |
|---|
Devices declared under this manufacturer
- KIJIMEA® COLON IRRITABILE PRO
- KIJIMEA® COLON IRRITABLE PRO
- KIJIMEA® CÔLON IRRITABLE PRO
- KIJIMEA® IBS PRO
- KIJIMEA® PRIKKELBARE DARM PRO
- KIJIMEA® REGULARIS
- KIJIMEA® REIZDARM
- KIJIMEA® REIZDARM PRO
- KIJIMEA® REIZMAGEN
Showing 12 of 31 declared devices.
European nomenclature codes declared: G0401.
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 | 28 |
|---|---|
| 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. Synformulas GmbH was not found in either the U.S. or the Canadian register.