- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
B-8012992BGMSSgluEJ2M41 reference
B-8012992BGMSSgluEJ2M4V10305320020Basic 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 →SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →European Medical Device Nomenclature — the EU product classifications carried across this device family's references.
W0101060101Glucose test strips1 reference
| Product | Trade name | Reference / catalog number | 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 → | Quantity | Status |
|---|---|---|---|---|---|
| GLUCOFIX TECH Sensor | GLUCOFIX TECH Sensor | 46627 NL, 46626, 46623 FR, 46622 FR10,47688 FR 50, 48587 IT, 48586 IT10, 48585 IT25, 48584 IT, 51342 UK, 51343 UK | D-8012992BGMSSgluEJ2M4 | 1 | On the market |