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h1 CLIA Microparticles

EUDAMED

Class B (EU MDR)

Ref CMQA1602Model AutoLumo Analyzer

by Autobio Diagnostics Co., Ltd.

Identity

Trade Name
h1 CLIA Microparticles EUDAMED
Device Name
h1 CLIA Microparticles EUDAMED
Model / Reference
AutoLumo Analyzer EUDAMED
CMQA1602 EUDAMED

Identifiers

Primary DI / UDI-DI
06942359510332 EUDAMED
Basic UDI-DI
697015090000247HL 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

Yes

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

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

h1 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 a7a091ba-5049-4830-bae9-6aa1d804f147 61 fields · synced Jun 18, 2026