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Bladder Cancer Urine Test

EUDAMED

Class IVD General (EU MDR)

Ref R01-110Ref R01-112Ref R01-112-01

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

Identity

Device Name
Bladder Cancer Urine Test EUDAMED
Model / Reference
R01-110 EUDAMED
R01-112 EUDAMED
R01-112-01 EUDAMED

Identifiers

Primary DI / UDI-DI
06941571801105 EUDAMED
06941571801211 EUDAMED
06941571801204 EUDAMED
Basic UDI-DI
B-06941571801105 EUDAMED
B-06941571801211 EUDAMED
B-06941571801204 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 Urine 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 (3)

  • EUDAMED 4b3b0b8d-c1b1-4e42-8f1f-2d6cb4a62c92 61 fields · synced Oct 6, 2026
  • EUDAMED 1185e3e1-cca9-46c1-95cc-6cf85c4d05d5 61 fields · synced May 17, 2026
  • EUDAMED 8050c12d-b4e1-48ee-ba22-7eff4d2e1582 61 fields · synced May 17, 2026