- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
B-8012992BGMSMgluketUV2EP1 reference
B-8012992BGMSMgluketUV2EPV10305320020Basic 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 stripsW010106010801Blood test strips controlsW0101060110Ketone test strips (β-hydroxybutyrate test strips)W020106019099Various diabetes monitoring instruments - other1 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 GK | GLUCOFIX TECH GK | 52076 FR/IT, 52077 FR-basic, 52078 NL, 56815 UK, 57170 FR-basic-E, 57168 FR, 57169 FR-E | D-8012992BGMSMgluketUV2EP | 1 | On the market |