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iFlash-CMV IgM

EUDAMED

Class C (EU MDR)

Ref C88033M-S

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Trade Name
iFlash-CMV IgM EUDAMED
Device Name
iFlash-CMV IgM EUDAMED
Model / Reference
C88033M-S EUDAMED

Identifiers

Primary DI / UDI-DI
06925912723622 EUDAMED
Basic UDI-DI
692591270104GW EUDAMED
EMDN Code
W0105040204 CMV IGM EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

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-CMV IgM by Shenzhen Yhlo Biotech Co., Ltd. — Class C — 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 db096f3c-aa1b-4689-aacb-a73ff520d6d8 61 fields · synced Jul 10, 2026