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f3 CLIA Microparticles

EUDAMED

Class B (EU MDR)

Ref CMQA0702Model AutoLumo Analyzer

by Autobio Diagnostics Co., Ltd.

Identity

Trade Name
f3 CLIA Microparticles EUDAMED
Device Name
f3 CLIA Microparticles EUDAMED
Model / Reference
AutoLumo Analyzer EUDAMED
CMQA0702 EUDAMED

Identifiers

Primary DI / UDI-DI
06942359509688 EUDAMED
Basic UDI-DI
697015090000238HK EUDAMED
EMDN Code
W01020202 IMMUNOGLOBULIN E - SPECIFIC, MONOTEST/MONORESULT 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

Category: Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent

f3 CLIA Microparticles by Autobio Diagnostics Co., Ltd. — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000003348
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 7fc28c14-e8a4-41e7-90af-c60c56d26b67 61 fields · synced Jun 18, 2026