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EUDAMED last updated this device on Jun 3, 2026
3770028922AX200TNBIOCHEMISTRY ANALYZER AX - 200CLOSED is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by GMT SARL. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
03770028922154AX200(01)03770028922154
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0201010101CHEMISTRY ANALYSERS - LOW ROUTINE (Random access without ISE mode test/h <= 400)2 warnings recorded — scroll inside the panel to see all entries.
CW008CW011FR-MF-000025248The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | — | Still on market |
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 →No certificate specifically references this device's Basic UDI-DI.
B-03770028922116On the marketAUTO HEMATOLOGY ANALYZER OX 560 - RETB-03770028922093On the marketAUTO HEMATOLOGY ANALYZER OX 560 - RET +B-03770028922109On the marketBIOCHEMISTRY ANALYZER AX - 200OPEN3770028922AX200TNOn the marketBIOCHEMISTRY ANALYZER AX - 300CLOSED3770028922AX000TCOn the marketBIOCHEMISTRY ANALYZER AX - 400CLOSED3770028922AX000TCOn 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.