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EUDAMED last updated this device on Apr 6, 2023
8058945153APL1000GNZ3aPL1000G is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by ABD SRL. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
080589451558068058945153APL1000GNZ3aPL1000G(01)08058945155806
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.
W0102010105IMMUNOGLOBULIN G3 warnings recorded — scroll inside the panel to see all entries.
CW010CW007CW032No certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Apr 29, 2021 | Dec 31, 2099 |
| Romania | Apr 29, 2021 | Dec 31, 2099 |
IT-MF-000029729No 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.