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Rotavirus Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref 808091-1

by Shenzhen Kang Sheng Bao Bio-Technology Co., Ltd.

Identity

Device Name
Rotavirus Rapid Test EUDAMED
Model / Reference
808091-1 EUDAMED

Identifiers

Primary DI / UDI-DI
D-808091-1BB EUDAMED
Basic UDI-DI
B-808091-1BB EUDAMED
EMDN Code
W0105099099 VIROLOGY - RT & POC - OTHER 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

Rotavirus Rapid Test by Shenzhen Kang Sheng Bao Bio-Technology 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-000024153
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 6bfd2536-2f5a-433c-b986-63a626abe8e2 61 fields · synced Jul 11, 2026