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iFlash-IgG1

EUDAMED

Class B (EU MDR)

Ref C86086G-SRef C86086G

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-IgG1 EUDAMED
Device Name
iFlash-IgG1 EUDAMED
Model / Reference
C86086G-S EUDAMED
C86086G EUDAMED

Identifiers

Primary DI / UDI-DI
06925912721222 EUDAMED
06925912720355 EUDAMED
Basic UDI-DI
692591270260HD EUDAMED
EMDN Code
W0102010106 IMMUNOGLOBULIN G SUBCLASS REAGENTS EUDAMED

Classification

Device Class
Class B 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-IgG1 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 (2)

  • EUDAMED 1dedb0dc-ca23-4786-83a6-6676832aa2ee 61 fields · synced Jul 12, 2026
  • EUDAMED 360e5443-58b8-4885-8c5a-0b1a53a654fc 61 fields · synced May 17, 2026