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Optitrol Yellow, 2x pos, 5mL

EUDAMED

Class B (EU MDR)

Ref SR11023Model SR11021

by LGC Clinical Diagnostics, Inc.

Identity

Trade Name
Optitrol Yellow, 2x pos, 5mL EUDAMED
Device Name
Optitrol Yellow 4x5 mL EUDAMED
Model / Reference
SR11021 EUDAMED
SR11023 EUDAMED

Identifiers

Primary DI / UDI-DI
00850075956715 EUDAMED
Basic UDI-DI
0816784020108XW EUDAMED
EMDN Code
W0105080807 MULTICONSTITUENT CONTROLS - INF.IMM. EUDAMED

Classification

Device Class
Class B 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

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

Yes

EUDAMED

Optitrol Yellow, 2x pos, 5mL by LGC Clinical 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-000016356
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (1)

  • EUDAMED 4b3f4526-eb06-4548-937a-584316ae07ee 61 fields · synced Jul 16, 2026