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Human chorionic gonadotropin Assay Kit (Chemiluminescent Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref S2091E-48Ref S2091E-24

by Sansure Biotech Inc.

Identity

Device Name
Human chorionic gonadotropin Assay Kit (Chemiluminescent Immunoassay) EUDAMED
Model / Reference
S2091E-48 EUDAMED
S2091E-24 EUDAMED

Identifiers

Primary DI / UDI-DI
06955792738232 EUDAMED
06955792738225 EUDAMED
Basic UDI-DI
B-06955792738232 EUDAMED
B-06955792738225 EUDAMED
EMDN Code
W0102050205 TOTAL HUMAN CHORIONIC GONADOTROPIN 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

Human chorionic gonadotropin Assay Kit (Chemiluminescent Immunoassay) by Sansure Biotech Inc. — 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-000011392
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED 1e9d731f-1524-4fa9-8ecb-b6ba702e7d7d 61 fields · synced Jul 28, 2026
  • EUDAMED 13ce5ac6-d779-4161-9d38-9a076d0a3037 61 fields · synced May 17, 2026