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EUDAMED last updated this device on Mar 6, 2026
697518250P117066RLuteinizing Hormone Determination Kit (Fluorescence Immunochromatographic Assay) is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class B. Manufactured by Beijing Diagreat Biotechnologies Co., Ltd.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06975182500102P11706CN-MF-000019511(01)06975182500102
The 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.
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 Italy; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Dec 1, 2023 | Dec 1, 2029 |
| Poland | Dec 1, 2023 | Dec 1, 2029 |
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0102050105LUTEINISING HORMONEPrimary 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.
697518250F1141223On the marketLipoprotein Phospholipase A2 Determination Kit (Fluorescence Immunochromatographic Assay)697518250P115086KOn the marketLuteinizing Hormone CLIA Kit (Chemiluminescence Immunoassay)697518250F117072ROn the marketLuteinizing Hormone Rapid Test Kit697518250G117022UOn the marketLysergic aciddiethylamide Panel Test Drugs of Abuse Test Kit697518250G127343GOn the marketMalaria P.f Antigen Rapid Test Kit697518250G1183138On 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.