MELIPHARM SAS
FR-MF-000031887 · France · PANAZOL
MELIPHARM SAS is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 6 |
|---|
Most frequent device types declared: DM1, DM2.
Among these devices, 6 are declared sterile.
Devices declared under this manufacturer
- Aristée Pollenergie\tMiel cicatrisant
- Cicatrimel Miel cicatrisant - Miel de thym et acide hyaluronique
- Cicatrimel Miel cicatrisant - Miel de thym et acide hyaluronique 30g
- Cicatrimel Miel cicatrisant - Miel de thym et acide hyaluronique 3x5g
- Melicare Gel Cicatrisant 30g
- Melicare Gel Cicatrisant 3x5g
Catalogue references include 1110_V2, 2051, 2058, 4011, 4012, 4018.
European nomenclature codes declared: M040499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| 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 | 6 |
|---|---|
| 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. MELIPHARM SAS was not found in either the U.S. or the Canadian register.