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MultiDrugs-5 Test panel F

EUDAMED

Class IVD General (EU MDR)

Ref R153-500F

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

Identity

Device Name
MultiDrugs-5 Test panel F EUDAMED
Model / Reference
R153-500F EUDAMED

Identifiers

Primary DI / UDI-DI
06941571815539 EUDAMED
Basic UDI-DI
B-06941571815539 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-5 Test panel F 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 6f3432e3-f643-46f2-a78d-be6b92d6ad05 61 fields · synced Jul 9, 2026