← Back to catalogue

iFlash-IGFBP-3

EUDAMED

Class B (EU MDR)

Ref C86127

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-IGFBP-3 EUDAMED
Device Name
iFlash-IGFBP-3 EUDAMED
Model / Reference
C86127 EUDAMED

Identifiers

Primary DI / UDI-DI
06925912720539 EUDAMED
Basic UDI-DI
692591270271HJ EUDAMED
EMDN Code
W0102060406 INSULIN-LIKE GROWTH FACTOR BINDING PROTEIN 3 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-IGFBP-3 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 63f85be0-9bf4-484c-abd0-a0383c4f5ce8 61 fields · synced Jul 18, 2026