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PCT Rapid Test

EUDAMED

Class C (EU MDR)

Ref CPC-N302-10

by Hangzhou Alltest Biotech.Co., Ltd.

Identity

Trade Name
PCT Rapid Test EUDAMED
Device Name
PCT Rapid Test EUDAMED
Model / Reference
CPC-N302-10 EUDAMED

Identifiers

Primary DI / UDI-DI
06936983104760 EUDAMED
Basic UDI-DI
6970277510000XYR EUDAMED
EMDN Code
W0102160999 INDIVIDUAL AND SPECIFIC HORMONES/PROTEINS RT & POC - OTHER EUDAMED

Classification

Device Class
Class C 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

New Device

No

EUDAMED

PCT Rapid Test by Hangzhou Alltest Biotech.Co., Ltd. — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Unknown

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000010710
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED c5505c9a-38bc-4ff5-83e6-e50125e4ad5c 61 fields · synced Jun 18, 2026