- Role
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- Date of registration
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EUDAMED last updated this device on Jun 9, 2026
B-8012992BGMSSgluEJ2M4GLUCOFIX TECH Sensor is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — Annex II List B. Manufactured by A. MENARINI Diagnostics S.r.l.. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
D-8012992BGMSSgluEJ2M446627 NL, 46626, 46623 FR, 46622 FR10,47688 FR 50, 48587 IT, 48586 IT10, 48585 IT25, 48584 IT, 51342 UK, 51343 UKIT-MF-000023427V10305320020D-8012992BGMSSgluEJ2M4
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
1 warning recorded — scroll inside the panel to see all entries.
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.
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.
Primary placement in France; available across 3 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Jun 16, 2015 | Dec 31, 2027 |
| Italy | Apr 29, 2019 | Dec 31, 2027 |
| Netherlands | Jun 16, 2015 | Dec 31, 2027 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0101060101GLUCOSE TEST STRIPSPrimary 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.
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.