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Prog Assay kit CLIA

EUDAMED

Class IVD General (EU MDR)

Ref SUPM061036Ref SUPM061072

by Shenzhen Superbio Technology Co., Ltd.

Identity

Trade Name
Prog Assay kit CLIA EUDAMED
Device Name
Prog Assay kit CLIA EUDAMED
Model / Reference
SUPM061036 EUDAMED
SUPM061072 EUDAMED

Identifiers

Primary DI / UDI-DI
06974521004349 EUDAMED
06974521004356 EUDAMED
Basic UDI-DI
B-06974521004349 EUDAMED
B-06974521004356 EUDAMED
EMDN Code
W0102050106 PROGESTERONE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

Prog Assay kit CLIA by Shenzhen Superbio Technology Co., Ltd. — 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-000024149
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (2)

  • EUDAMED d2a146a6-bb8a-49e5-af07-4c53e17514f7 61 fields · synced Aug 2, 2026
  • EUDAMED 34b8c2d2-39e8-4350-9679-ff150159106f 61 fields · synced May 18, 2026