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EUDAMED last updated this device on Sep 19, 2024
80593076401454V0018169040 is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class C. Manufactured by Instrumentation Laboratory SpA. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0805930764014580593076401454V0018169040(01)08059307640145
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.
W01010305LITHIUM3 warnings recorded — scroll inside the panel to see all entries.
CW082CW085CW999No certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 17 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Sep 18, 2024 | Still on market |
| Austria | Sep 18, 2024 | Still on market |
| Belgium | Sep 18, 2024 | Still on market |
| Cyprus | Sep 18, 2024 | Still on market |
| Germany | Sep 18, 2024 | Still on market |
| EL | Sep 18, 2024 | Still on market |
| Spain | Sep 18, 2024 | Still on market |
| Croatia | Sep 18, 2024 | Still on market |
| Ireland | Sep 18, 2024 | Still on market |
| Liechtenstein | Sep 18, 2024 | Still on market |
| Lithuania | Sep 18, 2024 | Still on market |
| Luxembourg | Sep 18, 2024 | Still on market |
| Malta | Sep 18, 2024 | Still on market |
| Netherlands | Sep 18, 2024 | Still on market |
| Poland | Sep 18, 2024 | Still on market |
| Romania | Sep 18, 2024 | Still on market |
| XI | Sep 18, 2024 | Still on market |
IT-MF-000009277Certificate health across this manufacturer's portfolio.
V12 034483 0002Issued