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Shigella Antigen Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref P221110

by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd.

Identity

Trade Name
Shigella Antigen Rapid Test EUDAMED
Device Name
Shigella Antigen Rapid Test EUDAMED
Model / Reference
P221110 EUDAMED

Identifiers

Primary DI / UDI-DI
16972698603706 EUDAMED
Basic UDI-DI
B-16972698603706 EUDAMED
EMDN Code
W0105090199 BACTERIOLOGY - RT & POC - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Spain 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

Shigella Antigen Rapid Test by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000013495
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 4fc51077-8644-4981-b8f4-9bd53ed3afdf 61 fields · synced Jun 18, 2026