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iFlash-CA50

EUDAMED

Class C (EU MDR)

Ref C86068-SRef C86068

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-CA50 EUDAMED
Device Name
iFlash-CA50 EUDAMED
Model / Reference
C86068-S EUDAMED
C86068 EUDAMED

Identifiers

Primary DI / UDI-DI
06925912721161 EUDAMED
06925912719380 EUDAMED
Basic UDI-DI
692591270160H8 EUDAMED
EMDN Code
W0102030104 CANCER ANTIGEN 50 EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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

iFlash-CA50 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 (2)

  • EUDAMED 3d5fac05-057d-4d81-a9fe-ac810630e3ab 61 fields · synced Jul 19, 2026
  • EUDAMED 389b2436-95c6-4727-90ec-49cdf31ef917 61 fields · synced May 18, 2026