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Feces Analysis System

EUDAMED

Class A (EU MDR)

Ref 2000RRef 50Ref 6000R

by Xiamen Sciendox Biological Technology Co., Ltd.

Identity

Device Name
Feces Analysis System EUDAMED
Model / Reference
2000R EUDAMED
50 EUDAMED
6000R EUDAMED

Identifiers

Primary DI / UDI-DI
06971124110002 EUDAMED
06971124110019 EUDAMED
06971124110026 EUDAMED
Basic UDI-DI
697112411FAS00137 EUDAMED
Direct Marketing DI
06971124110002 EUDAMED
06971124110019 EUDAMED
06971124110026 EUDAMED
EMDN Code
W0101060399 FAECES TESTS - RAPID TESTS AND "POINT OF CARE" - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Feces Analysis System by Xiamen Sciendox Biological Technology Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000029485
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (3)

  • EUDAMED ec48fb9c-83d6-4b35-81ec-48dbe4e1d5f4 61 fields · synced Aug 1, 2026
  • EUDAMED 5e1509ed-4bf6-4d8f-8552-4dc826ad643b 61 fields · synced May 18, 2026
  • EUDAMED 4c8b127a-0d7e-4fb2-a483-77e77d34c4c3 61 fields · synced May 19, 2026