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EUDAMED last updated this device on Jun 5, 2026
803377232DIA-601Y8M03331 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Medica S.p.A.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08033772321860803377232DIA-601Y8M03331(01)08033772321860
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
F01060103DIALYSERS - UFC < 18 ml/h/mmHg, SYNTHETIC MEMBRANES6 warnings recorded — scroll inside the panel to see all entries.
CW011CW010CW009CW001CW007CW032No certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 14 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jun 1, 2023 | Still on market |
| Austria | Jun 1, 2023 | Still on market |
| Czechia | Mar 14, 2025 | Still on market |
| Germany | Jun 1, 2023 | Still on market |
| EL | Jun 1, 2023 | Still on market |
| Spain | Jun 1, 2023 | Still on market |
| France | Jun 1, 2023 | Still on market |
| Ireland | Jun 1, 2023 | Still on market |
| Luxembourg | Jun 1, 2023 | Still on market |
| Portugal | Jun 1, 2023 | Still on market |
| Slovenia | Jun 1, 2023 | Still on market |
| Slovakia | Jun 1, 2023 | Still on market |
| Türkiye | Jun 1, 2023 | Still on market |
| XI | Jun 1, 2023 | Still on market |
IT-MF-000025691No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.