MEDIFORM S.A.
GR-MF-000034673 · Greece · Athens
MEDIFORM S.A. is registered in the European database on medical devices as a manufacturer, with 99 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 99 |
|---|
Devices declared under this manufacturer
- MEDIFORM HOSPITAL CARE PLUS Medium
- MEDIFORM MEDIPAD 60X90
- MEDIFORM Medipant Platinum Large
- MEDIFORM Medipant Super Large
- MEDIFORM Medipant X-Large
- MEDIFORM Medisafe Large
- MEDIFORM Medislip Maxi Xlarge
- MEDIFORM PREMIER 90X180
- MEDIFORM PREMIER ECONOMY Night X-Large
- MEDIFORM Perfect Πάνα Large
- MEDIFORM Premier Economy Large
- MEDIFORM Premier Golden Medium
Showing 12 of 99 declared devices.
Catalogue references include DHP2X36, DPE3X20, DPS2X32, PMEP314, PMEP412, PPR340.
European nomenclature codes declared: T99, T04010101, T04010299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 99 |
| Country of registration | Greece |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 99 |
|---|---|
| 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. MEDIFORM S.A. was not found in either the U.S. or the Canadian register.