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Differential Diagnosis Kit for Benign and Malignant Pulmonary Nodules (Reversib…

EUDAMED

Class IVD General (EU MDR)

Ref S302Model 96 tests/kit

by Ankang Euler Technology Co., LTD

Identity

Device Name
Differential Diagnosis Kit for Benign and Malignant Pulmonary Nodules (Reversible terminal termination method) EUDAMED
Model / Reference
96 tests/kit EUDAMED
S302 EUDAMED

Identifiers

Primary DI / UDI-DI
06975585300019 EUDAMED
Basic UDI-DI
B-06975585300019 EUDAMED
EMDN Code
W010699 GENETIC TESTS - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

No

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

Differential Diagnosis Kit for Benign and Malignant Pulmonary Nodules (Reversib… by Ankang Euler Technology Co., LTD — Class IVD General — IVDD — listed in…

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000027199
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 431600bd-7707-4a31-b72b-5010a719c91c 61 fields · synced Jul 31, 2026