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DE-MF-000013321nal von minden Drug-Screen® MDMA 500 Test is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by nal von minden GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jun 10, 2026
B-nvm-102008Q3Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
D-nvm-102008Q3
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 Germany; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Dec 31, 2029 |
| Austria | — | Dec 31, 2029 |
| Belgium | — | Dec 31, 2029 |
| Bulgaria | — | Dec 31, 2029 |
| Cyprus | — | Dec 31, 2029 |
| Czechia | — | Dec 31, 2029 |
| Denmark | — | Dec 31, 2029 |
| Estonia | — | Dec 31, 2029 |
| EL | — | Dec 31, 2029 |
| Spain | — | Dec 31, 2029 |
| Finland | — | Dec 31, 2029 |
| France | — | Dec 31, 2029 |
| Croatia | — | Dec 31, 2029 |
| Hungary | — | Dec 31, 2029 |
| Ireland | — | Dec 31, 2029 |
| Iceland | — | Dec 31, 2029 |
| Italy | — | Dec 31, 2029 |
| Liechtenstein | — | Dec 31, 2029 |
| Lithuania | — | Dec 31, 2029 |
| Luxembourg | — | Dec 31, 2029 |
| Latvia | — | Dec 31, 2029 |
| Malta | — | Dec 31, 2029 |
| Netherlands | — | Dec 31, 2029 |
| Norway | — | Dec 31, 2029 |
| Poland | — | Dec 31, 2029 |
| Portugal | — | Dec 31, 2029 |
| Romania | — | Dec 31, 2029 |
| Sweden | — | Dec 31, 2029 |
| Slovenia | — | Dec 31, 2029 |
| Slovakia | — | Dec 31, 2029 |
| Türkiye | — | Dec 31, 2029 |
| XI | — | Dec 31, 2029 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
D-nvm-102008Q3Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-nvm-102008Q3102008UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0102160502AMPHETAMINE/METHAMPHETAMINE SPECIFIC (+ECSTASY) - RT & POCNo certificate specifically references this device's Basic UDI-DI.
B-nvm-101079QKOn the marketnal von minden Drug-Screen® LSD 10 Test BarcodedB-nvm-102079BA87On the marketnal von minden Drug-Screen® MDMA 500 TestB-nvm-620105SBOn the marketnal von minden Drug-Screen® MDMA 500 TestB-nvm-101008PUOn the marketnal von minden Drug-Screen® MDPV 500 TestB-nvm-102076QLOn the marketnal von minden Drug-Screen® MET 1000 TestB-nvm-620025SCOn the marketCertificate health across this manufacturer's portfolio.
IX 1034230-2IssuedHX 1034230-1IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →Notified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →