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SARS-CoV-2 IgM Antibody Test Kit (Chemiluminescence Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref S2055E-150

by Sansure Biotech Inc.

Identity

Device Name
SARS-CoV-2 IgM Antibody Test Kit (Chemiluminescence Immunoassay) EUDAMED
Model / Reference
S2055E-150 EUDAMED

Identifiers

Primary DI / UDI-DI
06955792740136 EUDAMED
Basic UDI-DI
B-06955792740136 EUDAMED
EMDN Code
W0102010107 IMMUNOGLOBULIN M EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
France 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

A comprehensive medical device directory contains a detailed and accurate description of the SARS-CoV-2 IgM Antibody Test Kit (Chemiluminescence Immunoassay) including its features, compliance status, and FAQs.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

EUDAMED SRN
CN-MF-000011392
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 39e7d958-f7d1-4c76-898f-261deb08c491 61 fields · synced Jun 22, 2026