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EUDAMED last updated this device on Jun 11, 2026
40490550300001076UQGenoXtract® is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Hain Lifescience GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
040490550025048.31.01(01)04049055002504
European Medical Device Nomenclature — the EU product classification assigned to this device.
W02069099VARIOUS SAMPLE PROCESSING INSTRUMENTS - OTHER6 warnings recorded — scroll inside the panel to see all entries.
ISO7010: W009
ISO7010: W006 & P007
ISO7010: W004
ISO7010: W001
ISO7010: W017
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Still on market |
DE-MF-000008606The 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 →B-04049055000418On the marketGenoType NTM-DR VER 1.0B-04049055003235On the marketGenoType PAI-1 VER 2.0B-04049055000432On the marketGenoXtract® fleXT Software40490550300001089UZOn the marketGT-Blot 4840490550300001077USOn the marketGTQ-Cycler 9640490550300001083UMOn the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
V70 079456 0011IssuedV70 079456 0010IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →Notified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →