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EUDAMED last updated this device on Sep 27, 2023
8058945153AU2000/3GN4Evo Autoimmune Standard, anti-CL IgG 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.
080589451552713AU2000/3G(01)08058945155271
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0102152211STANDARDS AND CALIBRATORS FOR AUTOIMMUNITY3 warnings recorded — scroll inside the panel to see all entries.
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-000029729The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →IVDR risk classes
IVDR risk classes rank in-vitro diagnostic devices from lowest risk (Class A) to highest (Class D), based on the patient and public-health risk of a wrong result.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →8058945153AU2000/11LLOn the marketEvo Autoimmune Standard, anti-b2-GPI IgG8058945153AU2000/12GZ8On the marketEvo Autoimmune Standard, anti-b2-GPI IgM8058945153AU2000/12MZLOn the marketEvo Autoimmune Standard, anti-CL IgM8058945153AU2000/3MNGOn the marketEvo Autoimmune Standard, anti-DNA IgG8058945153AU2000/2DTOn the marketEvo Autoimmune Standard, anti-SSA IgG8058945153AU2000/1DROn the marketNo 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.No certificate specifically references this device's Basic UDI-DI.