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ARK Ethyl Glucuronide II Assay

EUDAMED

Class B (EU MDR)

Ref 5077-0001-00Ref 5077-0001-02Ref 5077-0001-03

by ARK Diagnostics, Inc.

Identity

Trade Name
ARK Ethyl Glucuronide II Assay EUDAMED
Device Name
ARK Ethyl Glucuronide II Assay EUDAMED
Model / Reference
5077-0001-00 EUDAMED
5077-0001-02 EUDAMED
5077-0001-03 EUDAMED

Identifiers

Primary DI / UDI-DI
00812101032084 EUDAMED
00812101032107 EUDAMED
00812101032114 EUDAMED
Basic UDI-DI
0858724003ETG0773H EUDAMED
Direct Marketing DI
00812101032084 EUDAMED
00812101032107 EUDAMED
00812101032114 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 Ethyl Glucuronide II 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 (3)

  • EUDAMED b35706b5-8c81-4263-a7ef-5b12cda19d18 61 fields · synced Jul 29, 2026
  • EUDAMED f69adaac-8798-4434-9d56-f1430343eca1 61 fields · synced May 16, 2026
  • EUDAMED be690a7a-3a33-40f9-968d-f0fb617c6f8d 61 fields · synced May 17, 2026