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Optitrol NAT Triplex, 5x 1, 2 mL

EUDAMED

Class B (EU MDR)

Ref NT01041

by LGC Clinical Diagnostics, Inc.

Identity

Trade Name
Optitrol NAT Triplex, 5x 1,2 mL EUDAMED
Device Name
Optitrol NAT Triplex, 5x 1,2 mL EUDAMED
Model / Reference
NT01041 EUDAMED

Identifiers

Primary DI / UDI-DI
00850075956326 EUDAMED
Basic UDI-DI
0816784020092Y8 EUDAMED
EMDN Code
W0105080808 ALL INFECTIOUS DISEASES CONTROLS - NAT 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 NAT Triplex, 5x 1, 2 mL 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 77e46ce5-5e40-44fe-b28c-6647fe99c740 61 fields · synced Jun 19, 2026