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Mycoplasma pneumoniae IgG/IgM Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref P231110

by Hangzhou Genesis Biodetection and Biocontrol Co., Ltd.

Identity

Trade Name
Mycoplasma pneumoniae IgG/IgM Rapid Test EUDAMED
Device Name
Mycoplasma pneumoniae IgG/IgM Rapid Test EUDAMED
Model / Reference
P231110 EUDAMED

Identifiers

Primary DI / UDI-DI
16972698601412 EUDAMED
Basic UDI-DI
B-16972698601412 EUDAMED
EMDN Code
W0105010802 MYCOPLASMA ANTIBODY ASSAYS 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

Yes

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

Mycoplasma pneumoniae IgG/IgM 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 cf405039-7c23-497b-9839-47660e8196c5 61 fields · synced Jun 18, 2026