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2019-nCoV IgM Antibody Determination Kit

EUDAMED

Class B (EU MDR)

Ref P11802Model 25 tests/box

by Beijing Diagreat Biotechnologies Co., Ltd.

Identity

Trade Name
2019-nCoV IgM Antibody Determination Kit EUDAMED
Device Name
2019-nCoV IgM Antibody Determination Kit EUDAMED
Model / Reference
25 tests/box EUDAMED
P11802 EUDAMED

Identifiers

Primary DI / UDI-DI
06942293581740 EUDAMED
Basic UDI-DI
697518250P118026N EUDAMED
Direct Marketing DI
06942293581740 EUDAMED
EMDN Code
W0105041104 CORONAVIRUS IGM EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

New Device

Yes

EUDAMED

2019-nCoV IgM Antibody Determination Kit by Beijing Diagreat Biotechnologies Co., Ltd. — Class B — 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-000019511
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED a25edcd0-a88c-4339-818b-56bfca20be31 61 fields · synced Jun 20, 2026