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Inuvi-006/CE Collection Kit

EUDAMED

Class A (EU MDR)

Ref Inuvi-006/CE

by Inuvi Diagnostics Limited

Identity

Trade Name
Inuvi-006/CE Collection Kit EUDAMED
Device Name
Inuvi-006/CE Collection Kit EUDAMED
Model / Reference
Inuvi-006/CE EUDAMED

Identifiers

Primary DI / UDI-DI
05061107470146 EUDAMED
Basic UDI-DI
5061107470146RH EUDAMED
Direct Marketing DI
05061107470146 EUDAMED
EMDN Code
W05019099 SAMPLES COLLECTION DEVICES - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

Yes

EUDAMED

Inuvi-006/CE Collection Kit by Inuvi Diagnostics Limited — Class A — 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
UK-MF-000049942
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 3ab93089-94c6-4e7e-87f8-acd8420199f0 61 fields · synced Jun 18, 2026