NEOMEDIS
FR-MF-000004432 · France · Paris
NEOMEDIS is registered in the European database on medical devices as a manufacturer, with 33 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 33 |
|---|
Most frequent device types declared: HPBB, HPFH, HPRX, HPSF, HPSG.
Devices declared under this manufacturer
- HYPOMER RELAX
- HYPOMER RELAX 50
- Hypomer Fresh 125
- Hypomer Relax 125
- Hypomer baby
- Hypomer fresh
- Hypomer soft
- Hypomer strong
- SNOTTY
- Zylomer Attack
- Zylomer Baby
- Zylomer Baby 50
Showing 12 of 33 declared devices.
Catalogue references include 11011FR, NA.
European nomenclature codes declared: Q030103.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 33 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 33 |
|---|---|
| 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. NEOMEDIS was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
146/MDR | supplemented | 2029-03-14 |