← Back to catalogue

iFlash-β2-Glycoprotein I IgM

EUDAMED

Class B (EU MDR)

Ref C89052M-S

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-β2-Glycoprotein I IgM EUDAMED
Device Name
iFlash-β2-Glycoprotein I IgM EUDAMED
Model / Reference
C89052M-S EUDAMED

Identifiers

Primary DI / UDI-DI
06925912723400 EUDAMED
Basic UDI-DI
692591270034H2 EUDAMED
EMDN Code
W0102100503 ANTI-B2-GLYCOPROTEIN I ANTIBODIES 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-β2-Glycoprotein I IgM 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 254a2585-04bc-494f-b5ec-ad0183601138 61 fields · synced Jun 11, 2026