Adria Med S.r.l.
IT-MF-000020866 · Italy · Tocco da Casauria (PE)
Adria Med S.r.l. is registered in the European database on medical devices as a manufacturer, with 284 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIb | 284 |
|---|
Most frequent device types declared: APO, APS, EASYFLOW, EASYFLOW-R, NHS.
Among these devices, 282 are declared sterile, 284 active.
Devices declared under this manufacturer
- APTĒ
- EASYFLOW
- EASYFLOW-R
- NEOPUMP
- NEOPUMP-R
- STEADYFLOW
Showing 12 of 284 declared devices.
Catalogue references include ABF0500R, LF0100RB, LF1500R, MF6000, NBF0200, NMF0150R.
European nomenclature codes declared: A05010101.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | ADRIA.MED. SRL (IT) · FDA 3013561817 |
| Devices in EUDAMED | 284 |
| Country of registration | Italy |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 284 |
|---|---|
| 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.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
026/MDR | issued | 2027-05-08 |