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EUDAMED last updated this device on Jul 21, 2026
376042770SEQUENCE86Sequence Evolution IVD is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by AD Nucleis. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
37604277000578SEQ_EVO_IVD(01)37604277000578
European Medical Device Nomenclature — the EU product classification assigned to this device.
W02050116NUCLEIC ACID TESTING INTEGRETED EXTRATION /AMPLIFICATION /DETECTION SYSTEMS1 warning recorded — scroll inside the panel to see all entries.
heatdeck inside may be hot
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Jan 18, 2024 | Still on market |
FR-MF-000002215The 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-37604277000028On the marketExtraction and purification kit of NA for blood 24R IVD376042770112B4On the marketExtraction purification kit of NA for blood 96R IVD376042770112B4On the marketSequence PREP IVD376042770SEQUENCE86On the marketThis device is used to extract DNA/RNA from EDTA blood samples376042770112B4On the marketNo certificate specifically references this device's Basic UDI-DI.
No 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.