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MultiDrugs-9 Test panel

EUDAMED

Class IVD General (EU MDR)

Ref R153-900

by Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd.

Identity

Device Name
MultiDrugs-9 Test panel EUDAMED
Model / Reference
R153-900 EUDAMED

Identifiers

Primary DI / UDI-DI
06941571815621 EUDAMED
Basic UDI-DI
B-06941571815621 EUDAMED
EMDN Code
W0102160511 MULTIPLE DRUGS OF ABUSE/TOXICOLOGY RT & POC EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

MultiDrugs-9 Test panel by Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000020607
Authorised Representative
CEpartner4U NL-AR-000000111

Sources (1)

  • EUDAMED 5ce1d153-9401-4560-9a89-b38e3966ea10 61 fields · synced Jun 19, 2026