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DRI Oxycodone

EUDAMED

Class B (EU MDR)

Ref 0018169540

by Instrumentation Laboratory SpA

Identity

Trade Name
DRI Oxycodone EUDAMED
Device Name
DRI Oxycodone EUDAMED
Model / Reference
0018169540 EUDAMED

Identifiers

Primary DI / UDI-DI
08059307640367 EUDAMED
Basic UDI-DI
80593076403675H EUDAMED
Direct Marketing DI
08059307640367 EUDAMED
EMDN Code
W0102090123 OXYCODINE EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Italy 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

DRI Oxycodone by Instrumentation Laboratory SpA — 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
IT-MF-000009277

Sources (1)

  • EUDAMED 1f0f0093-9f9e-475b-a221-fae7d6856bc0 61 fields · synced Jul 17, 2026