Eurofil S.r.l.
IT-MF-000026868 · Italy · Castilenti
Eurofil S.r.l. is registered in the European database on medical devices as a manufacturer, with 92 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 92 |
|---|
Devices declared under this manufacturer
- ASSORBENTI PER INCONTINENZA COOP MINI (12x20)
- ASSORBENTI PER INCONTINENZA COOP MUTANDINA MISURA MEDIA (4X15)
- BENNET PANNOLONE MUTANDINA LARGE C/B 4X15
- BENNET PANNOLONE MUTANDINA MEDIUM C/B 4X15
- CA DIFFUSION LADY COMFORT NORMAL NOUVEAU 12X20
- CA LADY COMFORT SUPER (LC SUPER) 8X20
- LADY CARE EXTRA 15x10
- PANTS PLUS ADVANTAGE CONAD TAGLIA GRANDE (4x8)
- SETTE LADY EXTRA 12x10
- TREKPLEISTER EVER FREE MINI PLUS 6X16
- TREKPLEISTER EXTRA PLUS 8x10
- VENIXE PANNOLONE MUTANDINA LARGE EXTRA ELASTIC 6X15
Showing 12 of 92 declared devices.
Catalogue references include 2207, 2674422_4, 2674430_4, 29341115, 3122091, 3496.
European nomenclature codes declared: T04010102, T04010103, T04010101, T04010201, T04010202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 92 |
| 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 | 92 |
|---|---|
| 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. Eurofil S.r.l. was not found in either the U.S. or the Canadian register.