- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Apr 15, 2026
B-DOA-A204aSLMulti-Drug Test Panel 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 Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
D-DOA-A204aSLDOA-A204aD-DOA-A204aSL
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0102160511MULTIPLE DRUGS OF ABUSE/TOXICOLOGY RT & POC1 warning recorded — scroll inside the panel to see all entries.
CN-MF-000028093Primary placement in Netherlands; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | — | Still on market |
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.
View in glossary →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.
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 →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 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.No certificate specifically references this device's Basic UDI-DI.
B-DOA-A77-0017VOn the marketMulti-Drug Test Cup (MET/COC/OXY/MOP/BZO/KET/THC/TRA/K2/K3/K4/MCAT/FTY/MTD/MDMA)B-DOA-A157-002XROn the marketMulti-Drug Test Cup (MOP/MET/KET/MDMA/THC)B-DOA-A57-00275On the marketMulti-Drug Test Panel (AMP/BZO/COC/MET/MDMA/ MOP/MTD/PCP/THC/SOMA/K2/K3/ETO)B-DOA-A134-002VWOn the marketMulti-Drug Test Panel (AMP/BAR/BZO/COC/MDMA/MET/MOP/MTD/TCA/THC)B-DOA-A104-005UVOn the marketMulti-Drug Test Panel (AMP/BAR/BZO/COC/MQL/MTD/OPI/PCP/PPX/THC)B-DOA-A104-006UXOn the market