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W0102069013

EUDAMED

Class IVD General (EU MDR)

Ref SUPM042072

by Shenzhen Superbio Technology Co., Ltd.

Identity

Trade Name
W0102069013 EUDAMED
Device Name
PCT Assay Kit CLIA EUDAMED
Model / Reference
SUPM042072 EUDAMED

Identifiers

Primary DI / UDI-DI
06974521001607 EUDAMED
Basic UDI-DI
B-06974521001607 EUDAMED
EMDN Code
W0102069013 PROCALCITONIN 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

W0102069013 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 (1)

  • EUDAMED 848446b8-5cef-4312-a72b-7024973f8168 61 fields · synced Aug 2, 2026