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EUDAMED last updated this device on Apr 9, 2026
B-DOA-A54-0146BMulti-Drug Test Panel (AMP/COC/MET/MOP/THC) is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by Hangzhou Aichek Medical Technology Co., Ltd.. Placed on the EU market in Spain. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
D-DOA-A54-0146BDOA-A54-014CN-MF-000028093D-DOA-A54-0146B
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
1 warning recorded — scroll inside the panel to see all entries.
CW010Sterile
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 Spain; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| SpainPrimary placement | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0102160511MULTIPLE DRUGS OF ABUSE/TOXICOLOGY RT & POCPrimary 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-DOA-A54-0166FOn the marketMulti-Drug Test Panel (AMP/COC/MDMA/MET/OPI/THC)B-DOA-A64-0096XOn the marketMulti-Drug Test Panel (AMP/COC/MET/BZO/BAR/MOP/THC/MDMA/MTD/PCP/OXY/BUP/TRA/K2)B-DOA-A144-003WDOn the marketMulti-Drug Test Panel (AMP/COC/MET/OPI/THC)B-DOA-A54-0056AOn the marketMulti-Drug Test Panel (AMP/COC/OPI/THC)B-DOA-A44-00965On the marketMulti-Drug Test Panel (AMP/MET/BZO/MOP/COC/THC)B-DOA-A64-0126LOn 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.