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Bladder Cancer Marker Test

EUDAMED

Class IVD General (EU MDR)

Ref R01S-112

by Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd.

Identity

Device Name
Bladder Cancer Marker Test EUDAMED
Model / Reference
R01S-112 EUDAMED

Identifiers

Primary DI / UDI-DI
06941571801006 EUDAMED
Basic UDI-DI
B-06941571801006 EUDAMED
EMDN Code
W0102160201 BTA - RT & POC EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany 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

Bladder Cancer Marker Test by Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000020607
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (1)

  • EUDAMED 3c57a481-3ce8-42af-8bb1-34a59a2422ea 61 fields · synced Aug 1, 2026