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QuicIgETM Aspergillus IgE Ab Lateral Flow Assay

EUDAMED

Class IVD General (EU MDR)

Ref DNK-1901-14Model 50 tests/kit

by Dynamiker Biotechnology (Tianjin) Co., Ltd.

Identity

Device Name
QuicIgETM Aspergillus IgE Ab Lateral Flow Assay EUDAMED
Model / Reference
50 tests/kit EUDAMED
DNK-1901-14 EUDAMED

Identifiers

Primary DI / UDI-DI
06930317801653 EUDAMED
Basic UDI-DI
B-06930317801653 EUDAMED
EMDN Code
W01020202 IMMUNOGLOBULIN E - SPECIFIC, MONOTEST/MONORESULT EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

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

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

QuicIgETM Aspergillus IgE Ab Lateral Flow Assay by Dynamiker Biotechnology (Tianjin) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

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/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000001133
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED c745ea03-f7d8-4be9-8d71-1b1290dea404 61 fields · synced Jul 9, 2026