ALPLA PHARMA GREECE Single Member S.Α.
EL-MF-000042547 · Greece · KOROPI-ATHENS
ALPLA PHARMA GREECE Single Member S.Α. is registered in the European database on medical devices as a manufacturer, with 28 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 28 |
|---|
Most frequent device types declared: DOSING CUP, DOSING SPOON, SPOON, VAGINAL APPLICATOR / RECTAL APPLICATOR.
Among these devices, 9 are declared with a measuring function.
Devices declared under this manufacturer
- CAP PROCTO-SYNALAR ASSEMBLED
- DOSING CUP 10 ML
- DOSING CUP 15 ML TRANSPARENT “N”
- DOSING CUP 20 ML
- DOSING SPOON 2,5/5 ML, WHITE ISPM15
- RECTAL CREAM APPLICATOR TRANSPARENT/WHITE
- RECTAL CREAM APPLICATOR WHITE/WHITE (SINGLE PACK)
- SPOON A1003
- VAGINAL APPLICATOR - 1/2 DOSE
- VAGINAL APPLICATOR - 1/2 DOSE (7 ITEMS)
- VAGINAL APPLICATOR N (3 PCS)
- VAGINAL APPLICATOR N (7 ITEMS)
Showing 12 of 28 declared devices.
Catalogue references include DOS20005, KOY2A300, KOY30006, POF06700, POF60062, POF60088.
European nomenclature codes declared: A0704.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 28 |
| 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 | 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. ALPLA PHARMA GREECE Single Member S.Α. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
1000239168 | supplemented | 2029-09-11 |