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iFlash-CRP

EUDAMED

Class C (EU MDR)

Ref C86310Ref C86310-L

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-CRP EUDAMED
Device Name
iFlash-CRP EUDAMED
Model / Reference
C86310 EUDAMED
C86310-L EUDAMED

Identifiers

Primary DI / UDI-DI
06925912719939 EUDAMED
06925912721833 EUDAMED
Basic UDI-DI
692591270265HP EUDAMED
EMDN Code
W01021109 C-REACTIVE PROTEIN 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

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-CRP 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 4adcbaee-bdb9-4ab1-96e2-5b86a0232b26 61 fields · synced Jul 30, 2026
  • EUDAMED 11128f8b-debf-4392-a1b3-94d0a80a861b 61 fields · synced May 18, 2026