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iFlash-PCT

EUDAMED

Class C (EU MDR)

Ref C86317

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-PCT EUDAMED
Device Name
iFlash-PCT EUDAMED
Model / Reference
C86317 EUDAMED

Identifiers

Primary DI / UDI-DI
06925912722991 EUDAMED
Basic UDI-DI
692591270050GY EUDAMED
EMDN Code
W0102069013 PROCALCITONIN EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Germany 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

New Device

No

EUDAMED

iFlash-PCT by Shenzhen Yhlo Biotech Co., Ltd. — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000001137
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED dc242816-4e01-4129-b1df-9caa38f8c2e8 61 fields · synced Jun 19, 2026