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iFlash-Cortisol

EUDAMED

Class B (EU MDR)

Ref C86034-S

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-Cortisol EUDAMED
Device Name
iFlash-Cortisol EUDAMED
Model / Reference
C86034-S EUDAMED

Identifiers

Primary DI / UDI-DI
06925912723349 EUDAMED
Basic UDI-DI
692591270045H7 EUDAMED
EMDN Code
W0102060203 CORTISOL EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Germany 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

iFlash-Cortisol by Shenzhen Yhlo Biotech Co., Ltd. — Class B — 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 0c0e064c-f1fb-4b1f-9fb9-2c2474872056 61 fields · synced Jul 21, 2026