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DRI Opiate

EUDAMED

Class B (EU MDR)

Ref W150135

by Instrumentation Laboratory SpA

Identity

Trade Name
DRI Opiate EUDAMED
Device Name
DRI Opiate EUDAMED
Model / Reference
W150135 EUDAMED

Identifiers

Primary DI / UDI-DI
08426950553113 EUDAMED
Basic UDI-DI
84269505531137M EUDAMED
Direct Marketing DI
08426950553113 EUDAMED
EMDN Code
W0102090113 OPIATES EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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 Opiate 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 b0210fcc-4f27-4e3a-b7b8-548a518e49e0 61 fields · synced Jul 25, 2026