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MDMA Panel Test Drugs of Abuse Test Kit

EUDAMED

Class B (EU MDR)

Ref G12710Model 25 tests/box

by Beijing Diagreat Biotechnologies Co., Ltd.

Identity

Trade Name
MDMA Panel Test Drugs of Abuse Test Kit EUDAMED
Device Name
MDMA Panel Test Drugs of Abuse Test Kit EUDAMED
Model / Reference
25 tests/box EUDAMED
G12710 EUDAMED

Identifiers

Primary DI / UDI-DI
06942293581474 EUDAMED
Basic UDI-DI
697518250G1271032 EUDAMED
Direct Marketing DI
06942293581474 EUDAMED
EMDN Code
W0102090102 AMPHETAMINE/METHAMPHETAMINE SPECIFIC EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

Yes

EUDAMED

MDMA Panel Test Drugs of Abuse Test Kit by Beijing Diagreat Biotechnologies Co., Ltd. — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000019511
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 0f130a5b-b4d6-459b-abe7-b2f0932fdf8a 61 fields · synced Jun 18, 2026