Pharmaflex S.r.l.
IT-MF-000036467 · Italy · Venafro
Pharmaflex S.r.l. is registered in the European database on medical devices as a manufacturer, with 44 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 44 |
|---|
Most frequent device types declared: Materasso; Topper, STANDARD H10; STANDARD H13,5; STANDARD H15; REFLUX; CERVICAL; BABY, Standard, Reflux, Standard; Hybrid.
Devices declared under this manufacturer
- Baby Topper
- GUANCIALe MEMORY PHARMAFLEX STANDARD H10
- Materasso Hybrid Francese King
- Materasso Hybrid Matrimoniale King
- Materasso Hybrid una piazza e mezza King
- Materasso Singolo King
- Materasso Standard Francese King
- Materasso Standard Matrimoniale King
- TOPPER ORTOPEDICO RELUX FRANCESE KING
- TOPPER ORTOPEDICO RELUX SINGOLO
- TOPPER ORTOPEDICO RELUX SINGOLO KING
- TOPPER ORTOPEDICO RELUX UNA PIAZZA E MEZZA
Showing 12 of 44 declared devices.
Catalogue references include 20201, 30100.02, 30100.08, 40100.03, 40100.08, 40200.01.
European nomenclature codes declared: V080702, V08030102, V028099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 44 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 44 |
|---|---|
| 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. Pharmaflex S.r.l. was not found in either the U.S. or the Canadian register.