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iFlash-IgG2

EUDAMED

Class B (EU MDR)

Ref C86087GRef C86087G-S

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-IgG2 EUDAMED
Device Name
iFlash-IgG2 EUDAMED
Model / Reference
C86087G EUDAMED
C86087G-S EUDAMED

Identifiers

Primary DI / UDI-DI
06925912720362 EUDAMED
06925912721239 EUDAMED
Basic UDI-DI
692591270261HF 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-IgG2 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 b3c1ddc8-5b3b-47d3-a0a4-de64b5911533 61 fields · synced Jul 26, 2026
  • EUDAMED 584e30d8-9543-4ee0-8dec-623a0a742293 61 fields · synced May 18, 2026