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Testosterone Assay Kit (Chemiluminescent Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref S2087E-48Ref S2087E-24

by Sansure Biotech Inc.

Identity

Device Name
Testosterone Assay Kit (Chemiluminescent Immunoassay) EUDAMED
Model / Reference
S2087E-48 EUDAMED
S2087E-24 EUDAMED

Identifiers

Primary DI / UDI-DI
06955792738157 EUDAMED
06955792738140 EUDAMED
Basic UDI-DI
B-06955792738157 EUDAMED
B-06955792738140 EUDAMED
EMDN Code
W0102050110 TESTOSTERONE (WITH DEHYDRO AND FREE TESTOSTERONE) 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

Testosterone Assay Kit (Chemiluminescent Immunoassay) by Sansure Biotech Inc. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

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 e8fafb80-8b3f-423e-934b-d1092a129240 61 fields · synced Jul 22, 2026
  • EUDAMED 25d4bf46-7a60-4416-989d-b60baa299b8b 61 fields · synced May 18, 2026