Materni
BE-MF-000035656 · Belgium · Erembodegem
Materni is registered in the European database on medical devices as a manufacturer, with 11 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 11 |
|---|
Most frequent device types declared: FlowCup, FlowSpoon, Teat.
Devices declared under this manufacturer
- FlowCup M1
- FlowCup M2
- FlowSpoon
- Speen, Eénmalig Gebruik, Large - Slow Flow
- Speen, Eénmalig gebruik, Large – Extra Fast Flow
- Speen, Eénmalig gebruik, Large – Fast Flow
- Speen, Eénmalig gebruik, Medium - Extra Fast Flow
- Speen, Eénmalig gebruik, Medium - Fast Flow
- Speen, Eénmalig gebruik, Medium - Slow Flow
- Speen, Eénmalig gebruik, Small
- mamivac® Babycup
Catalogue references include 281610, MEPA0012, MEPA0101, MEPA0103, MEPA0105, MEPA0115.
European nomenclature codes declared: V020380.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 11 |
| Country of registration | Belgium |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 11 |
|---|---|
| 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. Materni was not found in either the U.S. or the Canadian register.