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Early Diagnostic Kit for Urothelial Carcinoma (Reversible terminal termination …

EUDAMED

Class IVD General (EU MDR)

Ref S303Model 96 tests/kit

by Ankang Euler Technology Co., LTD

Identity

Device Name
Early Diagnostic Kit for Urothelial Carcinoma (Reversible terminal termination method) EUDAMED
Model / Reference
96 tests/kit EUDAMED
S303 EUDAMED

Identifiers

Primary DI / UDI-DI
06975585300026 EUDAMED
Basic UDI-DI
B-06975585300026 EUDAMED
EMDN Code
W01060215 BLADDER CANCER DETECTION / MONITORING 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

Early Diagnostic Kit for Urothelial Carcinoma (Reversible terminal termination … 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 b0a79760-46ca-448e-95b8-233237de1d8a 61 fields · synced Jun 18, 2026