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ARK Zopiclone Assay

EUDAMED

Class B (EU MDR)

Ref 5043-0001-00

by ARK Diagnostics, Inc.

Identity

Trade Name
ARK Zopiclone Assay EUDAMED
Device Name
ARK Zopiclone Assay EUDAMED
Model / Reference
5043-0001-00 EUDAMED

Identifiers

Primary DI / UDI-DI
00812101031308 EUDAMED
Basic UDI-DI
0858724003ZPC04399 EUDAMED
Direct Marketing DI
00812101031308 EUDAMED
EMDN Code
W0102090199 DRUGS OF ABUSE - OTHER EUDAMED

Classification

Device Class
Class B 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

New Device

No

EUDAMED

ARK Zopiclone Assay by Ark Diagnostics Inc — 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
US-MF-000023925
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 1ce2d65e-6118-4582-9f4d-28a0ce274681 61 fields · synced Jun 18, 2026