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ARK Ketamine II Assay

EUDAMED

Class B (EU MDR)

Ref 5083-0001-02Model 5083-0001-00Ref 5083-0001-01

by ARK Diagnostics, Inc.

Identity

Trade Name
ARK Ketamine II Assay EUDAMED
Device Name
ARK Ketamine II Assay EUDAMED
Model / Reference
5083-0001-00 EUDAMED
5083-0001-02 EUDAMED
5083-0001-01 EUDAMED

Identifiers

Primary DI / UDI-DI
00812101031612 EUDAMED
00812101031599 EUDAMED
00812101031605 EUDAMED
Basic UDI-DI
0858724003KET0833G EUDAMED
Direct Marketing DI
00812101031612 EUDAMED
00812101031599 EUDAMED
00812101031605 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

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

ARK Ketamine 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 db634c0d-25b2-47df-a7a1-466e4c3f259b 61 fields · synced Aug 4, 2026
  • EUDAMED 69cc98bc-8c05-4fa7-8870-95684365d26d 61 fields · synced May 17, 2026
  • EUDAMED ddf7fe31-3c2c-4b71-ab96-a6f5c3276ace 61 fields · synced May 19, 2026